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 the agency’s own highest classification or reported deaths or serious injuries, 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

13126–13150 of 18001

SevereFDA (Drugs)·D-0007-2016·2015-10-14
Merck Recalls Vytorin Tablets Due to Foreign Tablet Presence
Merck Sharp & Dohme is recalling specific bottles of Vytorin 10 mg/20 mg tablets because they contain 10 mg/40 mg tablets. The recall affects distribution in Kentucky, Mississippi, and Ohio.
Product
Vytorin (ezetimibe and simvastatin) tablets, 10 mg/20 mg, each tablet contains 10 mg ezetimibe and 20 mg simvastatin, Rx Only, 1000 count Bottle, Manuf. For Merck Sharp & Dohme Corp, a subsidiary of Merck & Co., Inc., Whitehouse Station, NJ 08889, NDC 66582-0312-82.
Category
Drug
Distribution
3 states
SevereFDA (Drugs)·D-0006-2016·2015-10-14
Sermorelin Injection Recalled Due to Sterility Assurance Concerns
DCA Pharmacy is recalling 129 vials of Sermorelin 6mg/6mL Lyophilized Powder because an FDA inspection found it was not compounded in an appropriate area, potentially compromising sterility.
Product
Sermorelin 6mg/6mL Lyophilized Powder, Sterile Compound for Subcutaneous Injection, Diabetes Corporation of America dba DCA Pharmacy, Franklin, TN 37064-5527
Category
Drug
Distribution
3 states
ModerateFDA (Drugs)·D-0008-2016·2015-10-14
Daytrana Methylphenidate Patches Recalled for Defective Delivery System
Noven Pharmaceuticals is recalling Daytrana (methylphenidate) 30 mg patches due to a defective delivery system that failed mechanical peel force specifications.
Product
DAYTRANA — DAYTRANA (METHYLPHENIDATE)
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1830-2015·2015-10-07
Hartley Medical Recalls Non-Sterile Prolotherapy with Phenol Vials
Hartley Medical Center Pharmacy is recalling 10 vials of Prolotherapy with Phenol due to non-sterility concerns. The product was distributed in California and Nevada.
Product
Prolotherapy with Phenol (Dextrose 25%, Glycerin 25%, Phenol 2.5%, QS SWI), 100 mL vial, Rx Only, Hartley Medical, (888) 671-2888
Category
Drug
Distribution
2 states
SevereFDA (Drugs)·D-1829-2015·2015-10-07
Hartley Medical Recalls Prolotherapy with Phenol Vials Due to Non-Sterility
Hartley Medical Center Pharmacy is recalling 14 vials of Prolotherapy with Phenol due to non-sterility concerns. The product was distributed in California and Nevada.
Product
Prolotherapy with Phenol (Dextrose 25%, Glycerin 10%, Lidocaine HCl 10%, Bupivacaine HCl 0.625%, Phenol 1%, QS SWI), 5 mL vial, Rx Only, Hartley Medical, (888) 671-2888
Category
Drug
Distribution
2 states
SevereFDA (Drugs)·D-1833-2015·2015-10-07
Medistat RX Recalls Sterile Products Due to Sterility Assurance Concerns
Medistat RX L.L.C. is recalling all sterile products, including various injectable medications, due to a lack of assurance of sterility.
Product
All Products Intended to be Sterile, mediStat Pharmacy, 110 East Azalea Ave., Foley, AL 36535, 844*737*2550. An Incomplete List of Recalled Products Includes 1) All Cyanacobalamin Products, 2) All Magnesium Chloride Products, 3) All Lipostat (MIC B12) Products, 4) All Trimix…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1832-2015·2015-10-07
Eagle Pharmacy Recalls Subpotent Lipo B Sterile Injection Vials
Eagle Pharmacy is recalling 104 vials of Lipo B Sterile Injection due to trace amounts of methylcobalamin. The product was distributed in Alabama and Tennessee.
Product
LIPO B STERILE INJECTION 10 mL ( Methionine 25 mg, Inositol 50 mg, Choline Chloride 50 mg, Pyridoxine Hydrochloride 5 mg, Methylcobalamin 0.1mg, Benzyl Alcohol, Sterile Water, Sodium Hydroxide, Hydrochloric Acid), Multidose vial, Rx Only, Compounded by Eagle Pharmacy…
Category
Drug
Distribution
2 states
ModerateFDA (Drugs)·D-0005-2016·2015-10-07
Guthy-Renker Recalls Subpotent Rodan & Fields Proactiv Foundation
Guthy-Renker LLC is recalling Rodan & Fields Proactiv Solution compact foundation because the salicylic acid ingredient is subpotent.
Product
Rodan & Fields Proactiv Solution, Sheer Finish Compact Foundation, salicylic acid acne treatment, DARK, 7 g/0.25 OZ. Compacts, Over the Counter. Manufactured for Guthy-Renker Palm Desert, CA 92250.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0001-2016·2015-10-07
Guthy-Renker Recalls Rodan & Fields Proactiv Foundation for Subpotent Salicylic Acid
Guthy-Renker LLC is recalling Rodan & Fields Proactiv Solution Compact Foundation because the salicylic acid ingredient is subpotent.
Product
Rodan & Fields Proactiv Solution, Sheer Finish Compact Foundation, salicylic acid acne treatment, FAIR, 7 g/0.25 OZ. Compacts, Over the Counter. Manufactured for Guthy-Renker Palm Desert, CA 92250.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0003-2016·2015-10-07
Guthy-Renker Recalls Subpotent Rodan & Fields Proactiv Foundation
Guthy-Renker LLC is recalling Rodan & Fields Proactiv Solution Compact Foundation because the salicylic acid ingredient is subpotent.
Product
Rodan & Fields Proactiv Solution, Sheer Finish Compact Foundation, salicylic acid acne treatment, MEDIUM, 7 g/0.25 OZ. Compacts, Over the Counter. Manufactured for Guthy-Renker Palm Desert, CA 92250.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1831-2015·2015-10-07
VistaPharm Recalls Metoclopramide Oral Solution Due to Defective Container Lids
VistaPharm is recalling 84,100 cups of Metoclopramide Oral Solution because the unit dose cup lids are not fully qualified.
Product
METOCLOPRAMIDE ORAL SOLUTION, USP 10 mg/10 mL, 10 mL cups, Rx only. Manufactured by VistaPharm, Inc, Largo, FL. NDC: 66689-031-01.
Category
Drug
Distribution
6 states
LowFDA (Drugs)·D-0004-2016·2015-10-07
Guthy-Renker Recalls Subpotent Rodan & Fields Proactiv Foundation
Guthy-Renker LLC is recalling specific lots of Rodan & Fields Proactiv Solution Compact Foundation because the salicylic acid ingredient is subpotent.
Product
Rodan & Fields Proactiv Solution, Sheer Finish Compact Foundation, salicylic acid acne treatment, TAN, 7 g/0.25 OZ. Compacts, Over the Counter. Manufactured for Guthy-Renker Palm Desert, CA 92250.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0002-2016·2015-10-07
Rodan & Fields Proactiv Foundation Recalled for Subpotent Salicylic Acid
Guthy-Renker LLC is recalling Rodan & Fields Proactiv Solution compact foundation because the salicylic acid ingredient is subpotent.
Product
Rodan & Fields Proactiv Solution, Sheer Finish Compact Foundation, salicylic acid acne treatment, LIGHT, 7 g/0.25 OZ. Compacts, Over the Counter. Manufactured for Guthy-Renker Palm Desert, CA 92250.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D1834-2015·2015-10-07
Apotex Recalls Verapamil Hydrochloride Extended-Release Tablets for Dissolution Failure
Apotex Inc. is recalling 2,075 bottles of Verapamil Hydrochloride Extended-Release tablets, 240 mg, because one lot failed to meet dissolution specification limits.
Product
Verapamil Hydrochloride Extended-Release tablets, USP, 240 mg, 500-count bottles, Rx Only, Apotex Corp. Manufactured by Apotex Research Private Limited, Bangalore, Karnataka 560 099, India; Manufactured for: Apotex Corp., Weston, FL 33326. NDC 60505-2742-5.
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1823-2015·2015-09-30
PharMEDium Recalls Bupivacaine Bags Due to Human Hair Particulate Matter
PharMEDium Services is recalling 20 bags of Bupivacaine HCl 0.0625% for epidural use because they contain human hair particulate matter.
Product
Bupivacaine HCl 0.0625%, 250 mL total volume in a 250 mL LifeCare Bag in Sodium chloride 0.9%, Epidural Use Only, Rx Only, PharMEDium Services, LLC, 6100 Global Drive, Memphis, TN 36141, NDC# 61553-197-50
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1824-2015·2015-09-30
PharMEDium Recalls Morphine Sulfate IV Bags Due to Particulate Matter
PharMEDium Services is recalling 100 bags of Morphine Sulfate IV solution because the sodium chloride used contained human hair.
Product
Morphine Sulfate, 1 mg per mL (250 mg per 250 mL), 250 mL total volume in a 250 mL LifeCare bag in Sodium Chloride 0.9%, IV Use Only, Rx only, PharMEDium Services, LLC, 6100 Global Drive, Memphis, TN 36141, NDC# 61553-181-50
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1816-2015·2015-09-30
Baxter Recalls Sodium Chloride Injection Bags Due to Sterility Concerns
Baxter Healthcare is recalling 139,104 bags of 0.9% Sodium Chloride Injection due to a reported complaint of mold on the interior surface of the overpouch.
Product
SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1828-2015·2015-09-30
Pharmedium Recalls Phenylephrine Injection Bags Due to Particulate Matter
Pharmedium Services is recalling 120 bags of Phenylephrine HCl injection due to the presence of human hair particulate matter.
Product
PHENYLephrine HCl, 10 mg added to 250 mL 0.9% Sodium Chloride Injection USP (40 mcg per mL), packaged in 250 ml bags, Rx only, PharMEDium Services, LLC, 12620 W. Airport Blvd., Sugar Land, TX 77478, NDC# 61553-149-50
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1827-2015·2015-09-30
Pharmedium Phenylephrine Injection Recalled for Particulate Matter
Pharmedium Services, LLC is recalling 48 bags of Phenylephrine HCl injection due to the presence of particulate matter, specifically human hair, in the product.
Product
PHENYLephrine HCl, 60 mg added to 250 mL 0.9% Sodium Chloride Injection USP (240 mcg per mL), packaged in 250 ml bags, Rx only, PharMEDium Services, LLC, 12620 W. Airport Blvd., Sugar Land, TX 77478, NDC# 61553-236-50
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1826-2015·2015-09-30
Pharmedium Recalls Phenylephrine Injection Due to Human Hair Particulate Matter
Pharmedium Services is recalling 84 bags of Phenylephrine HCl injection because the sodium chloride base contained human hair.
Product
PHENYLephrine HCl, 20 mg added to 250 mL 0.9% Sodium Chloride Injection USP (80 mcg per mL), packaged in 250 ml bags, Rx only, PharMEDium Services, LLC, 12620 W. Airport Blvd., Sugar Land, TX 77478, NDC# 61553-156-50
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1821-2015·2015-09-30
Pharmedium Recalls Phenylephrine Injection Due to Human Hair Contamination
Pharmedium Services, LLC is recalling specific lots of Phenylephrine HCl injection because the sodium chloride base used contained human hair.
Product
PHENYLephrine HCl, 50 mg added to 250 mL 0.9% Sodium Chloride Injection USP (200 mcg per mL), packaged in 250 ml bags, Rx only, PharMEDium Services, LLC, 12620 W. Airport Blvd., Sugar Land, TX 77478, NDC# 61553-171-50
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1825-2015·2015-09-30
PharMEDium Recalls Fentanyl Citrate IV Bags Due to Particulate Matter
PharMEDium Services, LLC is recalling 663 bags of Fentanyl Citrate IV solution because the sodium chloride used contained human hair.
Product
Fentanyl Citrate, 5 mcg per mL (1,250 mcg per 250 mL), 250 mL total volume in a 250 mL LifeCare bag in Sodium Chloride 0.9%, IV Use Only, Rx only, PharMEDium Services, LLC, 6100 Global Drive, Memphis, TN 36141, NDC# 61553-107-50
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1822-2015·2015-09-30
Pharmedium Recalls Phenylephrine Injection Due to Human Hair Particulate Matter
Pharmedium Services is recalling specific lots of Phenylephrine HCl injection due to the presence of human hair particulate matter.
Product
PHENYLephrine HCl, 40 mg added to 250 mL 0.9% Sodium Chloride Injection USP (160 mcg per mL), packaged in 250 ml bags, Rx only, PharMEDium Services, LLC, 12620 W. Airport Blvd., Sugar Land, TX 77478, NDC# 61553-169-50
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1815-2015·2015-09-30
Hospira Recalls Lidocaine Hydrochloride Injection Due to Particulate Matter
Hospira, Inc. is recalling Lidocaine Hydrochloride Injection vials because iron oxide particulate matter was found embedded in the glass vial necks.
Product
LIDOCAINE HYDROCHLORIDE — LIDOCAINE HYDROCHLORIDE (LIDOCAINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1819-2015·2015-09-30
Allergan Recalls FML Ophthalmic Ointment Due to Particulate Matter
Allergan is recalling specific lots of FML ophthalmic ointment because small black particles from the tube cap may be present in the product.
Product
FML (fluorometholone ophthalmic ointment) 0.1%, 3.5 g tube, Rx only, Allergan, Inc., Irvine, CA 92612, NDC 0023-0316-04, UPC 3 0023-0316-04 0.
Category
Drug
Distribution
Distributed nationwide

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13126–13150 of 18001