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Drug Recalls

Last updated

Every drug recall in FDA enforcement reports from the last three years, plus older recalls that are still open. Filter by severity, status or medicine, and check the lot numbers on your package.

3 Class I (most serious) drug recalls reported in the last 30 days.

3,250 recalls

  • Class II Ongoing

    Pyridoxine HCL 100 mg/ml, (30 ML). Compounded by Tri-Coast Pharmacy

    Reason: Lack of Assurance of Sterility

    Tri-Coast Pharmacy · Pyridoxine Hydrochloride

    Lots, distribution and details
    Product
    Pyridoxine HCL 100 mg/ml, (30 ML). Compounded by Tri-Coast Pharmacy
    Lots / codes
    Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 08162016A (02/12/2017).
    Distribution
    Nationwide
    Quantity
    3 vials
    Recall started
    November 17, 2016 (Voluntary: Firm initiated)
    Severity
    Could cause temporary or medically reversible health problems; serious harm is unlikely.
    FDA recall number
    D-0279-2017
  • Class II Ongoing

    Nandrolone Decanoate 200 mg/ml, (5 ML). Compounded by Tri-Coast Pharmacy

    Reason: Lack of Assurance of Sterility

    Tri-Coast Pharmacy

    Lots, distribution and details
    Product
    Nandrolone Decanoate 200 mg/ml, (5 ML). Compounded by Tri-Coast Pharmacy
    Lots / codes
    Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 07112016A (12/31/2016), 08172016B (2/13/2017), 09122016C (02/28/2017), 10252016E (02/28/2017).
    Distribution
    Nationwide
    Quantity
    701 vials
    Recall started
    November 17, 2016 (Voluntary: Firm initiated)
    Severity
    Could cause temporary or medically reversible health problems; serious harm is unlikely.
    FDA recall number
    D-0278-2017
  • Class II Ongoing

    Mineral Mix Schrader, Zinc Chloride 5 mg/ml + Vanadium 100 mcg/ml + Manganese HCL 100 mcg/ml + Sodium Molybdate 250 mcg/ml + Strontium Chloride 3 mg/ml + Lithium Citrate 5 mg/ml + Chromium Picolinate 100 mcg/ml + Boron C…

    Reason: Lack of Assurance of Sterility

    Tri-Coast Pharmacy

    Lots, distribution and details
    Product
    Mineral Mix Schrader, Zinc Chloride 5 mg/ml + Vanadium 100 mcg/ml + Manganese HCL 100 mcg/ml + Sodium Molybdate 250 mcg/ml + Strontium Chloride 3 mg/ml + Lithium Citrate 5 mg/ml + Chromium Picolinate 100 mcg/ml + Boron Citrate 1798 mg/ml + Sodium Selenite 200 mcg.ml + Cupric Sulfate 1 mg/ml, (30 ML). Compounded by Tri-Coast Pharmacy
    Lots / codes
    Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 05182016B (11/14/2016), 08102016B (12/31/2016)
    Distribution
    Nationwide
    Quantity
    36 vials
    Recall started
    November 17, 2016 (Voluntary: Firm initiated)
    Severity
    Could cause temporary or medically reversible health problems; serious harm is unlikely.
    FDA recall number
    D-0277-2017
  • Class II Ongoing

    MIC Ultra Cocktail (Methionine (L) 25mg/Inositol 50mg/Choline Chloride 50mg/Methylcobalamin 700mcg/Chromium Picolinate 20 mcg/Pyridoxine HCL 2mg/ml), (10 ML). Compounded by Tri-Coast Pharmacy

    Reason: Lack of Assurance of Sterility

    Tri-Coast Pharmacy

    Lots, distribution and details
    Product
    MIC Ultra Cocktail (Methionine (L) 25mg/Inositol 50mg/Choline Chloride 50mg/Methylcobalamin 700mcg/Chromium Picolinate 20 mcg/Pyridoxine HCL 2mg/ml), (10 ML). Compounded by Tri-Coast Pharmacy
    Lots / codes
    Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 06132016B (11/30/2016), 08042016B (12/31/2016), 08252016A (12/31/2016)
    Distribution
    Nationwide
    Quantity
    278 vials
    Recall started
    November 17, 2016 (Voluntary: Firm initiated)
    Severity
    Could cause temporary or medically reversible health problems; serious harm is unlikely.
    FDA recall number
    D-0276-2017
  • Class II Ongoing

    Myers Cocktail #5 (Ascorbic Acid 2000 mg + Magnesium Chloride 1000 mg + Calcium Gluconate (Anhydrous) 200 mg + Pyridoxine HCL 100 mg + Dexpanthenol 252 mg + Methylcobalamin 2 mg + Thiamine HCL 100 mg + Riboflavin-5-Phosp…

    Reason: Lack of Assurance of Sterility

    Tri-Coast Pharmacy

    Lots, distribution and details
    Product
    Myers Cocktail #5 (Ascorbic Acid 2000 mg + Magnesium Chloride 1000 mg + Calcium Gluconate (Anhydrous) 200 mg + Pyridoxine HCL 100 mg + Dexpanthenol 252 mg + Methylcobalamin 2 mg + Thiamine HCL 100 mg + Riboflavin-5-Phosphate Sod 2 mg + Folic Acid 1 mg + Vitamin E Succinate 10 IU + Vitamin A Acetate 100 IU/10-mL), (10 ML). Compounded by Tri-Coast Pharmacy
    Lots / codes
    Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 07182016A (12/31/2016)
    Distribution
    Nationwide
    Quantity
    21 vials
    Recall started
    November 17, 2016 (Voluntary: Firm initiated)
    Severity
    Could cause temporary or medically reversible health problems; serious harm is unlikely.
    FDA recall number
    D-0275-2017
  • Class II Ongoing

    Myers Cocktail #4 (Ascorbic Acid 2000 mg + Magnesium Chloride 1000 mg + Calcium Gluconate (Anhydrous) 200 mg + Pyridoxine HCL 100 mg + Dexpanthenol 252 mg + Methylcobalamin 2 mg + Thiamine HCL 100 mg + Riboflavin-5-Phosp…

    Reason: Lack of Assurance of Sterility

    Tri-Coast Pharmacy

    Lots, distribution and details
    Product
    Myers Cocktail #4 (Ascorbic Acid 2000 mg + Magnesium Chloride 1000 mg + Calcium Gluconate (Anhydrous) 200 mg + Pyridoxine HCL 100 mg + Dexpanthenol 252 mg + Methylcobalamin 2 mg + Thiamine HCL 100 mg + Riboflavin-5-Phosphate Sod 2 mg/10-mL), (10 ML). Compounded by Tri-Coast Pharmacy
    Lots / codes
    Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 06202016DD (06/21/2016), 09132016B (02/28/2017)
    Distribution
    Nationwide
    Quantity
    66 vials
    Recall started
    November 17, 2016 (Voluntary: Firm initiated)
    Severity
    Could cause temporary or medically reversible health problems; serious harm is unlikely.
    FDA recall number
    D-0274-2017
  • Class II Ongoing

    Methylcobalamin/Folic Acid/Pyridoxine 1 mg/1 mg/50 mg/mL, 1 ML). Compounded by Tri-Coast Pharmacy

    Reason: Lack of Assurance of Sterility

    Tri-Coast Pharmacy

    Lots, distribution and details
    Product
    Methylcobalamin/Folic Acid/Pyridoxine 1 mg/1 mg/50 mg/mL, 1 ML). Compounded by Tri-Coast Pharmacy
    Lots / codes
    Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 05232016A (05/06/2016), 06282016B (07/01/2016), 06212016A (06/24/2016), 06142016A (06/17/2016), 06072016E (06/10/2016), 06022016B (06/05/2016), 06022016A (06/05/2016), 07262016H (07/29/2016), 07192016A (07/22/2016), 07122016A (07/15/2016), 07082016D (07/11/2016), 07062016B (07/09/2016), 08302016B (09/03/2016), 08232016D (08/26/2016), 08162016D (08/19/2016), 08092016E (08/11/2016), 08042016F (08/07/2016), 09272016D (09/30/2016), 09272016B (09/30/2016), 09202016A (09/23/2016), 09132016A (09/16/2016), 09072016B (09/10/2016), 10112016D (10/14/2016), 10042016B (10/07/2016), 11022016A (11/05/2016), 11092016A (11/12/2016), 11082016A (11/11/2016)
    Distribution
    Nationwide
    Quantity
    99 vials
    Recall started
    November 17, 2016 (Voluntary: Firm initiated)
    Severity
    Could cause temporary or medically reversible health problems; serious harm is unlikely.
    FDA recall number
    D-0273-2017
  • Class II Ongoing

    Methylcobalamin 1,000 mcg/mL, 10 mL and 30 mL. Compounded by Tri-Coast Pharmacy

    Reason: Lack of Assurance of Sterility

    Tri-Coast Pharmacy

    Lots, distribution and details
    Product
    Methylcobalamin 1,000 mcg/mL, 10 mL and 30 mL. Compounded by Tri-Coast Pharmacy
    Lots / codes
    Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 05312016KK, 05262016A (11/22/2016), 060920161 (12/06/2016), 07262016B (01/22/2017), 07062016C (12/31/2016), 08292016B (02/25/2017), 10132016F (04/11/2017), 10252016K (02/28/2017), 07262016C (01/22/2017), 09152016 (02/28/2017)
    Distribution
    Nationwide
    Quantity
    1,458 vials
    Recall started
    November 17, 2016 (Voluntary: Firm initiated)
    Severity
    Could cause temporary or medically reversible health problems; serious harm is unlikely.
    FDA recall number
    D-0272-2017
  • Class II Ongoing

    Lipotropic with MIC (Methionine (L) 12.5mg/Inositol 25mg/Choline Chloride 25mg/L-Carnitine 170 mg + Methylcopalamin 300 mcg + Thiamine HCL 20 mg + Riboflavin-5-Phosphate Sod 2 mg + Niacinamide 20 mg + Pyridoxine HCL 2 mg…

    Reason: Lack of Assurance of Sterility

    Tri-Coast Pharmacy

    Lots, distribution and details
    Product
    Lipotropic with MIC (Methionine (L) 12.5mg/Inositol 25mg/Choline Chloride 25mg/L-Carnitine 170 mg + Methylcopalamin 300 mcg + Thiamine HCL 20 mg + Riboflavin-5-Phosphate Sod 2 mg + Niacinamide 20 mg + Pyridoxine HCL 2 mg + Folic Acid 1 mg/Lidocaine HCL 20mg/ml, (30 ML). Compounded by Tri-Coast Pharmacy
    Lots / codes
    Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 06012016B (11/28/2016), 07082016A (12/31/2016), 08242016C (12/31/2016)
    Distribution
    Nationwide
    Quantity
    236 vials
    Recall started
    November 17, 2016 (Voluntary: Firm initiated)
    Severity
    Could cause temporary or medically reversible health problems; serious harm is unlikely.
    FDA recall number
    D-0271-2017
  • Class II Ongoing

    Lipotropic (L-Carnitine 170 mg + Methylcobalamin 300 mcg + Thiamine HCL 20 mg + Riboflavin-5-phosphate Sod 2 mg + Niacinamide 20 mg + Pyridoxine HCL 2 mg + Folic Acid 1 mg/Lidocaine HCL 10 mg/ml), (30 ML). Compounded by…

    Reason: Lack of Assurance of Sterility

    Tri-Coast Pharmacy

    Lots, distribution and details
    Product
    Lipotropic (L-Carnitine 170 mg + Methylcobalamin 300 mcg + Thiamine HCL 20 mg + Riboflavin-5-phosphate Sod 2 mg + Niacinamide 20 mg + Pyridoxine HCL 2 mg + Folic Acid 1 mg/Lidocaine HCL 10 mg/ml), (30 ML). Compounded by Tri-Coast Pharmacy
    Lots / codes
    Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 09022016A (12/31/2016), 07282016C (12/31/2016)
    Distribution
    Nationwide
    Quantity
    987 vials
    Recall started
    November 17, 2016 (Voluntary: Firm initiated)
    Severity
    Could cause temporary or medically reversible health problems; serious harm is unlikely.
    FDA recall number
    D-0270-2017
  • Class II Ongoing

    Lipo-C (Methionine 25 mg/Inositol 50 mg/Choline Chloride 50 mg/Carnitine (L) 100 mg/Methylcobalamin 1 mg/Thiamine HCL 50 mg/Rivoflavin-5-Phosphate Sod 5 mg/Niacinamide 50 mg/Dexpanthenol 5 mg/Pyridoxine HCL 1.25 mg/Lidoc…

    Reason: Lack of Assurance of Sterility

    Tri-Coast Pharmacy

    Lots, distribution and details
    Product
    Lipo-C (Methionine 25 mg/Inositol 50 mg/Choline Chloride 50 mg/Carnitine (L) 100 mg/Methylcobalamin 1 mg/Thiamine HCL 50 mg/Rivoflavin-5-Phosphate Sod 5 mg/Niacinamide 50 mg/Dexpanthenol 5 mg/Pyridoxine HCL 1.25 mg/Lidocaine HCL 10 mg/mL), (30 ML). Compounded by Tri-Coast Pharmacy
    Lots / codes
    Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 07282016B (12/31/2016), 08242016B (12/31/2016)
    Distribution
    Nationwide
    Quantity
    69 vials
    Recall started
    November 17, 2016 (Voluntary: Firm initiated)
    Severity
    Could cause temporary or medically reversible health problems; serious harm is unlikely.
    FDA recall number
    D-0269-2017
  • Class II Ongoing

    L-Tyrosine 10 mg/mL, (30 ML). Compounded by Tri-Coast Pharmacy

    Reason: Lack of Assurance of Sterility

    Tri-Coast Pharmacy

    Lots, distribution and details
    Product
    L-Tyrosine 10 mg/mL, (30 ML). Compounded by Tri-Coast Pharmacy
    Lots / codes
    Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 07292016A (01/25/2017), 07182016E (01/14/2017), 08222016A (02/28/2017), 10192016A (10/22/2016)
    Distribution
    Nationwide
    Quantity
    50 vials
    Recall started
    November 17, 2016 (Voluntary: Firm initiated)
    Severity
    Could cause temporary or medically reversible health problems; serious harm is unlikely.
    FDA recall number
    D-0268-2017
  • Class II Ongoing

    L-Carnitine 250 mg/mL, (30 ML). Compounded by Tri-Coast Pharmacy

    Reason: Lack of Assurance of Sterility

    Tri-Coast Pharmacy

    Lots, distribution and details
    Product
    L-Carnitine 250 mg/mL, (30 ML). Compounded by Tri-Coast Pharmacy
    Lots / codes
    Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 09132016F (02/28/2017).
    Distribution
    Nationwide
    Quantity
    14 vials
    Recall started
    November 17, 2016 (Voluntary: Firm initiated)
    Severity
    Could cause temporary or medically reversible health problems; serious harm is unlikely.
    FDA recall number
    D-0267-2017
  • Class II Ongoing

    L-Arginine HCL 100 mg/mL, (30 ML). Compounded by Tri-Coast Pharmacy

    Reason: Lack of Assurance of Sterility

    Tri-Coast Pharmacy

    Lots, distribution and details
    Product
    L-Arginine HCL 100 mg/mL, (30 ML). Compounded by Tri-Coast Pharmacy
    Lots / codes
    Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 07282016H (01/24/2017), 09282016E (03/27/2017)
    Distribution
    Nationwide
    Quantity
    41 vials
    Recall started
    November 17, 2016 (Voluntary: Firm initiated)
    Severity
    Could cause temporary or medically reversible health problems; serious harm is unlikely.
    FDA recall number
    D-0266-2017
  • Class II Ongoing

    IV Cocktail #2 (Ascorbic Acid 200 mg+Vitamin A Acetate 330 IU+Vitamin D3 200 IU+Thiamine HCL 6 mg+Riboflavin-5-Phosphate Sod 3.6 mg+Pyridoxine HCL 6 mg+Niacinamide 40 mg+Dexpanthenol 15 mg+Vitamin 40E Succinate 10 IU+Phy…

    Reason: Lack of Assurance of Sterility

    Tri-Coast Pharmacy

    Lots, distribution and details
    Product
    IV Cocktail #2 (Ascorbic Acid 200 mg+Vitamin A Acetate 330 IU+Vitamin D3 200 IU+Thiamine HCL 6 mg+Riboflavin-5-Phosphate Sod 3.6 mg+Pyridoxine HCL 6 mg+Niacinamide 40 mg+Dexpanthenol 15 mg+Vitamin 40E Succinate 10 IU+Phytonadione (K1) 150 mcg/5 mL), (30 ML). Compounded by Tri-Coast Pharmacy
    Lots / codes
    Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date, if known): 05252016D (05/28/2016), 05202016A (05/23/2016), 05182016C (05/21/2016), 05092016C (05/12/2016), 05022016C (05/05/2016), 06132016D (06/16/2016), 06072016A (06/10/2016), 06062016A (06/09/2016), 07282106E (07/31/2016), 07252016G (07/28/2016), 09122016A (09/15/2016), 09192016B (09/22/2016)
    Distribution
    Nationwide
    Quantity
    132 vials
    Recall started
    November 17, 2016 (Voluntary: Firm initiated)
    Severity
    Could cause temporary or medically reversible health problems; serious harm is unlikely.
    FDA recall number
    D-0265-2017
  • Class II Ongoing

    Infuvite IV (Ascorbic Acid 200 mg+ Vitamin A Acetate 330 IU+Vitamin D3 200 IU+Thiamine HCL 6 mg+Riboflavin-5-Phosphate Sod 3.6 mg+Pyridoxine HCL 6 mg+Niacinamide 40 mg+Dexpanthenol 15 mg+Vitamin 40E Succinate 10 IU+Phyto…

    Reason: Lack of Assurance of Sterility

    Tri-Coast Pharmacy

    Lots, distribution and details
    Product
    Infuvite IV (Ascorbic Acid 200 mg+ Vitamin A Acetate 330 IU+Vitamin D3 200 IU+Thiamine HCL 6 mg+Riboflavin-5-Phosphate Sod 3.6 mg+Pyridoxine HCL 6 mg+Niacinamide 40 mg+Dexpanthenol 15 mg+Vitamin 40E Succinate 10 IU+Phytonadione (K1) 150 mcg/5 mL). 30 ML. Compounded by Tri-Coast Pharmacy.
    Lots / codes
    Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date, if known): 07062016D (10/30/2016), 08312016A, 08232016C, 08222016C, 08102016E, 08102016D, 08012016E, 09262016C, 09132016C
    Distribution
    Nationwide
    Quantity
    161 vials
    Recall started
    November 17, 2016 (Voluntary: Firm initiated)
    Severity
    Could cause temporary or medically reversible health problems; serious harm is unlikely.
    FDA recall number
    D-0264-2017
  • Class II Ongoing

    HCG 11,000 IU Vial. Compounded by Tri-Coast Pharmacy

    Reason: Lack of Assurance of Sterility

    Tri-Coast Pharmacy

    Lots, distribution and details
    Product
    HCG 11,000 IU Vial. Compounded by Tri-Coast Pharmacy
    Lots / codes
    Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 06152016A (12/12/2016), 07252016D (01/21/2017), 07112016C (01/07/2017), 08312016B (02/27/2017), 08262016B (02/22/2017), 08092016D (02/05/2017), 08052016A (02/01/2017), 09282016B (02/28/2017), 09222016D (02/28/2017), 09072016A (02/28/2017), 10252016J (02/28/2017), 10182016D (02/28/2017), 10102016H (02/28/2017), 11042016A (02/28/2017), 11012016E (02/28/2017)
    Distribution
    Nationwide
    Quantity
    5,229 vials
    Recall started
    November 17, 2016 (Voluntary: Firm initiated)
    Severity
    Could cause temporary or medically reversible health problems; serious harm is unlikely.
    FDA recall number
    D-0263-2017
  • Class II Ongoing

    HCG/Hydroxycobalamin 5,000 IU/5 mg Vial. Compounded by Tri-Coast Pharmacy

    Reason: Lack of Assurance of Sterility

    Tri-Coast Pharmacy

    Lots, distribution and details
    Lots / codes
    Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 06232016A (12/20/2016), 07192016B (01/15/2017), 08262016A (01/31/2017), 08092016C (01/31/2017), 09192016C (01/31/2017), 11042016C (11/04/2016), 10252016A (02/28/2017)
    Distribution
    Nationwide
    Quantity
    1,304 vials
    Recall started
    November 17, 2016 (Voluntary: Firm initiated)
    Severity
    Could cause temporary or medically reversible health problems; serious harm is unlikely.
    FDA recall number
    D-0262-2017
  • Class II Ongoing

    HCG 5,000 IU Vial. Compounded by Tri-Coast Pharmacy.

    Reason: Lack of Assurance of Sterility

    Tri-Coast Pharmacy

    Lots, distribution and details
    Product
    HCG 5,000 IU Vial. Compounded by Tri-Coast Pharmacy.
    Lots / codes
    Lot codes: 06222016D, 06062016C, 07192016C07062016A, 08182016B, 08112016A, 08012016A, 09282016A, 09122016D, 10182016C, 11042016B, 11012016F; Exp. 11/16
    Distribution
    Nationwide
    Quantity
    4,884 vials
    Recall started
    November 17, 2016 (Voluntary: Firm initiated)
    Severity
    Could cause temporary or medically reversible health problems; serious harm is unlikely.
    FDA recall number
    D-0261-2017
  • Class II Ongoing

    Glutathione 200 mg/mL (30 ML). Compounded by Tri-Coast Pharmacy

    Reason: Lack of Assurance of Sterility

    Tri-Coast Pharmacy

    Lots, distribution and details
    Product
    Glutathione 200 mg/mL (30 ML). Compounded by Tri-Coast Pharmacy
    Lots / codes
    Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 06082016A (09/06/2016), 07052016C (10/03/2016), 08082016A (11/06/2016), 09132016D (12/12/2016), 10262016A (01/24/2016).
    Distribution
    Nationwide
    Quantity
    367 vials
    Recall started
    November 17, 2016 (Voluntary: Firm initiated)
    Severity
    Could cause temporary or medically reversible health problems; serious harm is unlikely.
    FDA recall number
    D-0260-2017
  • Class II Ongoing

    Glutamine 25 mg/mL (30 ML). Compounded by Tri-Coast Pharmacy

    Reason: Lack of Assurance of Sterility

    Tri-Coast Pharmacy

    Lots, distribution and details
    Product
    Glutamine 25 mg/mL (30 ML). Compounded by Tri-Coast Pharmacy
    Lots / codes
    Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp date): 08032016A (01/30/2017).
    Distribution
    Nationwide
    Quantity
    12 vials
    Recall started
    November 17, 2016 (Voluntary: Firm initiated)
    Severity
    Could cause temporary or medically reversible health problems; serious harm is unlikely.
    FDA recall number
    D-0259-2017
  • Class II Ongoing

    Glucosamine 200 mg/mL (30 ML). Compounded by Tri-Coast Pharmacy

    Reason: Lack of Assurance of Sterility

    Tri-Coast Pharmacy

    Lots, distribution and details
    Product
    Glucosamine 200 mg/mL (30 ML). Compounded by Tri-Coast Pharmacy
    Lots / codes
    Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 10192016D (10/22/2016).
    Distribution
    Nationwide
    Quantity
    30 vials
    Recall started
    November 17, 2016 (Voluntary: Firm initiated)
    Severity
    Could cause temporary or medically reversible health problems; serious harm is unlikely.
    FDA recall number
    D-0258-2017
  • Class II Ongoing

    GAC, L-Glutamine/L-Arginine/L-Carnitine 25 mg/100 mg/200 mg/mL (30 mL). Tri-Coast Pharmacy.

    Reason: Lack of Assurance of Sterility

    Tri-Coast Pharmacy

    Lots, distribution and details
    Product
    GAC, L-Glutamine/L-Arginine/L-Carnitine 25 mg/100 mg/200 mg/mL (30 mL). Tri-Coast Pharmacy.
    Lots / codes
    Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 06172016A (12/14/2016), 08092016B (02/05/2014), 09262016A (03/25/2017), 10132016E (02/28/2017).
    Distribution
    Nationwide
    Quantity
    114 vials
    Recall started
    November 17, 2016 (Voluntary: Firm initiated)
    Severity
    Could cause temporary or medically reversible health problems; serious harm is unlikely.
    FDA recall number
    D-0257-2017
  • Class II Ongoing

    Dexpanthenol 250 mg/mL (30 ML). Compounded by Tri-Coast Pharmacy

    Reason: Lack of Assurance of Sterility

    Tri-Coast Pharmacy

    Lots, distribution and details
    Product
    Dexpanthenol 250 mg/mL (30 ML). Compounded by Tri-Coast Pharmacy
    Lots / codes
    Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 08162016B (02/12/2017).
    Distribution
    Nationwide
    Quantity
    5 vials
    Recall started
    November 17, 2016 (Voluntary: Firm initiated)
    Severity
    Could cause temporary or medically reversible health problems; serious harm is unlikely.
    FDA recall number
    D-0256-2017
  • Class II Ongoing

    Calm Me (Aminobutyric Acid (GABA) 50 mg/Magnesium Chloride 50 mg/Taurine 50 mg/Theanine (L) 50 mg/Tryptophan (L) 10 mg/Lidocaine HCL 10 mg/ml), (30 ML). Compounded by Tri-Coast Pharmacy.

    Reason: Lack of Assurance of Sterility

    Tri-Coast Pharmacy

    Lots, distribution and details
    Product
    Calm Me (Aminobutyric Acid (GABA) 50 mg/Magnesium Chloride 50 mg/Taurine 50 mg/Theanine (L) 50 mg/Tryptophan (L) 10 mg/Lidocaine HCL 10 mg/ml), (30 ML). Compounded by Tri-Coast Pharmacy.
    Lots / codes
    Recall includes all sterile products compounded between 05/17/2016 and 11/17/2016. Known lot codes (Exp Date): 09212016A (01/31/2017), 08032016C (01/31/2017).
    Distribution
    Nationwide
    Quantity
    10 vials
    Recall started
    November 17, 2016 (Voluntary: Firm initiated)
    Severity
    Could cause temporary or medically reversible health problems; serious harm is unlikely.
    FDA recall number
    D-0255-2017

Have this medicine at home? Compare the lot number and expiry date on your package with the recall. Do not stop taking a prescribed medicine on your own — stopping suddenly can be riskier than the recalled lot. Your pharmacist can check it and usually swap it for an unaffected one.

What the recall classes mean

  • Class I Most serious: use could cause serious health problems or death.
  • Class II Could cause temporary or medically reversible health problems; serious harm is unlikely.
  • Class III Not likely to cause health problems — for example a labelling or packaging fault.

Source: FDA Enforcement Report, via openFDA. Updated here twice a day; last update November 5, 2026 14:40. openFDA data are not validated for clinical use — confirm with the FDA source or your pharmacist.

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