Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

7926–7950 of 11823

SevereFDA (Drugs)·D-0575-2016·2016-01-27
FDA Recalls Energique Homeopathic Skin Spray Due to Microbial Contamination
Grato Holdings, Inc. is recalling 118 bottles of Energique homeopathic skin spray due to out-of-specification microbial counts.
Product
Energique, Homeopathic Remedy, Skin Irritant & Healing Support, Topical Spray, 1 fl oz bottle, NDC 44911-0136-1, Dist. by Energique, Inc., Woodbine, IA; ALSO LABELED AS --- Liddell Laboratories, Skin Irritant & Healing Support, Topical Homeopathic Spray, NDC 50845-0214-1, Dist By
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0584-2016·2016-01-27
Pine Pharmaceuticals Recalls Bevacizumab Syringes Due to Silicone Oil Particulates
Pine Pharmaceuticals is recalling specific lots of bevacizumab syringes for intravitreal injection because they contain silicone oil microdroplets.
Product
Bevacizumab 2.5 mg/0.1 mL in 3/10 mL 31 G 5/16" Syringe for intravitreal injection, Rx -- Pine Pharmaceuticals, 100 Colvin Woods Pkwy Suite 300, Tonawanda, NY 14150.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0577-2016·2016-01-27
Energique Joint Pain Spray Recalled for Microbial Contamination
Grato Holdings is recalling Energique Joint Pain & Stiffness Relief Topical Spray due to microbial contamination. Testing revealed out-of-specification results for total aerobic microbiological count.
Product
Energique, Homeopathic Remedy, Joint Pain & Stiffness Relief, Topical Spray, 1 fl oz (30 ml) bottles, NDC 44911-0133-1, Dist. by Energique, Inc., Woodbine, IA; ALSO LABELED AS --- Liddell Laboratories, Joint Pain & Stiffness Relief, Topical Homeopathic Spray, NDC 50845-0218-1, Di
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0581-2016·2016-01-27
Pine Pharmaceuticals Recalls Bevacizumab Syringes Due to Silicone Oil Particulates
Pine Pharmaceuticals is recalling Bevacizumab syringes for intravitreal use because they contain silicone oil microdroplets.
Product
Bevacizumab 1.25 mg/0.05 mL in 3/10 mL 31 G 5/16" Syringe for intravitreal Rx -- Pine Pharmaceuticals, 100 Colvin Woods Pkwy Suite 300, Tonawanda, NY 14150.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0580-2016·2016-01-27
FDA Recalls Energique Homeopathic Pain Spray for Microbial Contamination
Grato Holdings is recalling Energique First Aid Pain & Trauma Relief homeopathic spray due to out-of-specification microbial counts.
Product
Energique, Homeopathic Remedy, First Aid Pain & Trauma Relief, 1 fl oz (30 ml) bottles, NDC 44911-0135-1, Dist. by Energique, Inc., Woodbine, IA; ALSO LABELED AS --- Liddell Laboratories, First Aid Pain & Trauma Relief, Topical Homeopathic Spray, NDC 50845-0216-1, Dist By Liddell
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0570-2016·2016-01-27
Amerita Recalls Baclofen and Clonidine Syringes Due to Sterility Concerns
Amerita Specialty Infusion Services is recalling specific lots of compounded intrathecal syringes because the company cannot ensure they are sterile.
Product
IT Custom Compound (BC) Baclofen 2000 mcg/ml, Clonidine 2 mcg/ml 40 ml PF syringe, FOR INTRATHECAL USE ONLY, Rx Only, Compounded by Amerita, Inc., Prescott, AZ 86305-1614
Category
Drug
Distribution
0 states
SevereFDA (Drugs)·D-0582-2016·2016-01-27
Pine Pharmaceuticals Recalls Bevacizumab Syringes Due to Silicone Oil Microdroplets
Pine Pharmaceuticals is recalling specific lots of bevacizumab syringes for intravitreal use due to the presence of silicone oil microdroplets.
Product
Bevacizumab 1.25 mg/0.05 mL filled to 0.06 mL in 3/10 mL 31 G 5/16" Syringe for intravitreal, Rx -- Pine Pharmaceuticals, 100 Colvin Woods Pkwy Suite 300, Tonawanda, NY 14150.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0569-2016·2016-01-27
Amerita Recalls Baclofen Syringes Due to Sterility Assurance Concerns
Amerita Specialty Infusion Services is recalling specific lots of compounded Baclofen syringes because the FDA identified a lack of assurance of sterility.
Product
Baclofen 1 mg/ml in 40 ml NS syringe, FOR INTRATHECAL USE ONLY, Rx Only, Compounded by Amerita, Inc., Prescott, AZ 86305-1614
Category
Drug
Distribution
0 states
SevereFDA (Drugs)·D-0585-2016·2016-01-27
Mylan Bromfenac Ophthalmic Solution Recalled for Sterility Assurance Failure
Mylan Pharmaceuticals is recalling specific lots of Bromfenac Ophthalmic Solution 0.09% because the preservative failed an effectiveness test, raising concerns about sterility.
Product
Bromfenac Ophthalmic Solution 0.09%, a) 2.5 mL bottles (NDC 0378-7110-35) and b) 5 mL bottles (NDC 00378-7109-35), Rx only, Mylan Pharmaceuticals, Inc., Morgantown, WV 26505
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0573-2016·2016-01-27
Freedom Pharmaceuticals Recalls Baclofen Powder Due to Foreign Substance
Freedom Pharmaceuticals is recalling specific lots of Baclofen USP powder because of the presence of a foreign substance.
Product
Baclofen USP powder, packaged in (a) 25gm (4 oz container), (b) 100gm (16 oz container), (c) 500 gm (70 oz container), and (d) 1000 gm (120 oz container, Rx only, 801 W New Orleans St. Broken Arrow, OK 74011. NDC: (a) 52372-0909-25; (b) 52372-0909-01; (c) 52372-0909-50; (d) 523
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0583-2016·2016-01-27
Pine Pharmaceuticals Recalls Bevacizumab Syringes Due to Silicone Oil Microdroplets
Pine Pharmaceuticals is recalling specific lots of Bevacizumab syringes for intravitreal use because they contain silicone oil microdroplets.
Product
Bevacizumab 2 mg/0.08 mL in 3/10 mL 31 G 5/16" Syringe for intravitreal, Rx -- Pine Pharmaceuticals, 100 Colvin Woods Pkwy Suite 300, Tonawanda, NY 14150.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0565-2016·2016-01-20
Amerisource Recalls Hydrochlorothiazide Capsules Due to Particulate Matter
Amerisource Health Services is recalling specific lots of Hydrochlorothiazide capsules because they contain particulate matter.
Product
HYDROCHLOROTHIAZIDE CAPSULES, USP, 12.5 mg, 10 cap/blister, 100-count carton, Rx only, Packaged and Distributed by American Health Packaging Columbus, Ohio 43217, NDC 68084-0398-01
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0567-2016·2016-01-20
Freedom Pharmaceuticals Recalls Domperidone API Due to Penicillin Cross-Contamination
Freedom Pharmaceuticals is recalling specific lots of Domperidone API for prescription compounding due to potential cross-contamination with penicillin.
Product
Domperidone BP, Active Pharmaceutical Ingredient for Prescription Compounding, packaged in a) 5 gm (NDC: 52372-0898-01), b) 25 gm (NDC: 52372-0898-02), c) 100 gm (NDC: 52372-0898-03), and d) 500 gm (NDC: 52372-0898-04), Cas No. 57808-66-9, Rx only, FREEDOM, 801 W. New Orleans St.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0558-2016·2016-01-06
Walgreens Recalls 3-in-1 TPN Formula Bags Due to Sterility Concerns
Walgreens Infusion Services is recalling 87 bags of 3-in-1 TPN formula in Texas due to a lack of assurance of sterility.
Product
3-in-1 TPN formula daily+overfill Bag, 2000 mL, Rx Only, Compounded by Option Care 148, San Antonio, TX 78232-5045
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-0550-2016·2016-01-06
Clindamycin Injection Bags Recalled for Lack of Sterility Assurance
Walgreens Infusion Services is recalling Clindamycin injection Accuflo bags in Texas due to a lack of assurance of sterility.
Product
Clindamycin injection, Accuflo bag, a) 500 mg/NS 50 mL b) 900 mg/NS 100 mL, Rx Only, Compounded by Option Care 148, San Antonio, TX 78232-5045
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-0542-2016·2016-01-06
Walgreens Recalls Thiamine Syringes Due to Sterility Concerns
Walgreens Infusion Services is recalling 23 Thiamine 100 mg syringes in Texas due to a lack of assurance of sterility.
Product
Thiamine 100 mg (1 mL) syringe, Rx Only, Compounded by Option Care 148, San Antonio, TX 78232-5045
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-0557-2016·2016-01-06
Walgreens Recalls 0.9% Sodium Chloride/MVI Injection Bags Due to Sterility Concerns
Walgreens Infusion Services is recalling 7 bags of 0.9% Sodium Chloride/MVI injection in Texas due to a lack of assurance of sterility.
Product
0.9% Sodium Chloride/MVI injection 2000 mL Bag, Rx Only, Compounded by Option Care 148, San Antonio, TX 78232-5045
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-0547-2016·2016-01-06
Walgreens Recalls IVIG Gammagard Injection Bags Due to Sterility Concerns
Walgreens Infusion Services is recalling five bags of IVIG Gammagard injection in Texas due to a lack of assurance of sterility.
Product
IVIG Gammagard injection bag, a) 13 gm, b) 20 gm, c) 73 gm, Rx Only, Compounded by Option Care 148, San Antonio, TX 78232-5045
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-0536-2016·2016-01-06
Meropenem Infusion Minibags Recalled for Sterility Assurance Concerns
Walgreens Infusion Services is recalling 35 Meropenem minibags distributed in Texas due to a lack of assurance of sterility.
Product
Meropenem 1 g/NS 100 mL Minibag Plus, Rx Only, Compounded by Option Care 148, San Antonio, TX 78232-5045
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-0552-2016·2016-01-06
Remicade Injection Recalled for Lack of Sterility Assurance
Walgreens Infusion Services is recalling Remicade (Infliximab) injection bags in Texas due to a lack of assurance of sterility.
Product
Remicade (Infliximab) injection, 5 mg/kg bag, Rx Only, Compounded by Option Care 148, San Antonio, TX 78232-5045
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-0528-2016·2016-01-06
Walgreens Recalls Vancomycin Injection Bags Due to Sterility Concerns
Walgreens Infusion Services is recalling 95 bags of Vancomycin Injection in NS due to a lack of assurance of sterility. The affected products were distributed in Texas.
Product
Vancomycin Injection in NS, Accuflo bag, a) 500 mg/NS 100 mL, b)1G/NS 100 mL, c) Vancomycin 1G/NS 250 mL, d) 1.5G/NS 250 mL e) 750 mg/NS 100 mL, Rx Only, Compounded by Option Care 148, San Antonio, TX 78232-5045
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-0526-2016·2016-01-06
Walgreens Recalls Pedi MVI Syringes Due to Sterility Concerns
Walgreens Infusion Services is recalling 73 syringes of Pedi MVI in Texas due to a lack of assurance of sterility.
Product
Pedi MVI a) 5 mL, b) 10 mL syringe, Rx Only, Compounded by Option Care 148, San Antonio, TX 78232-5045
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-0544-2016·2016-01-06
Walgreens Recalls Sodium Ascorbate Syringes Due to Sterility Concerns
Walgreens Infusion Services is recalling compounded Sodium Ascorbate (Vitamin C) syringes in Texas due to a lack of assurance of sterility.
Product
Sodium Ascorbate (Vitamin C) syringe, a) 500 mg/1 mL syringe, b)1000 mg/2 mL c) 800 mg/1.6 mL, Rx Only, Compounded by Option Care 148, San Antonio, TX 78232-5045
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-0549-2016·2016-01-06
Gentamicin Syringes Recalled for Lack of Sterility Assurance
Walgreens Infusion Services is recalling 27 prefilled Gentamicin syringes in Texas due to a lack of assurance of sterility.
Product
Gentamicin 14.4 mg/sodium chloride 0.9% 30 mL Prefilled syringe, Rx Only, Compounded by Option Care 148, San Antonio, TX 78232-5045
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-0556-2016·2016-01-06
Walgreens Recalls 0.9% Sodium Chloride Injection Bags Due to Sterility Concerns
Walgreens Infusion Services is recalling 43 bags of 0.9% Sodium Chloride injection in Texas due to a lack of assurance of sterility.
Product
0.9% Sodium Chloride injection bag, a) 500 mL, b)1000 mL c)2000 mL Bag, Rx Only, Compounded by Option Care 148, San Antonio, TX 78232-5045
Category
Drug
Distribution
1 state

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7926–7950 of 11823