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

12226–12250 of 17785

LowFDA (Drugs)·D-0734-2016·2016-03-09
J. Strickland Recalls Subpotent Sulfur8 Anti-Dandruff Conditioner
J. Strickland and Co is recalling Sulfur8 Medicated Light Formula anti-dandruff conditioner because it failed stability testing. The product is subpotent.
Product
sulfur8 medicated LIGHT FORMULA (sulfur) anti-dandruff hair & scalp conditioner, 2%, packaged in a) 2 OZ (57g) jar (UPC 0 75610 43510 8), and b) 4 OZ (113g) jar (UPC 0 75610 43610 5), 1 dozen jars per case, J. Strickland & Co., PO Box 1637, Olive Branch, MS 38654
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0726-2016·2016-03-02
Keystone Recalls Medicated Better Braids Spray Due to Staphylococcus aureus
Keystone Laboratories is recalling Medicated Better Braids, La Laque (salicylic acid) Spray due to a positive Staphylococcus aureus test result.
Product
Medicated Better Braids, La Laque (salicylic acid) Spray, 2%,12 Fl. OZ. (355 ml.) bottle, Distributed by Keystone Laboratories, Memphis, TN 38101-2026, UPC 0 70596 00422 5.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0725-2016·2016-03-02
Zydus Recalls Risperidone Tablets Due to Impurity Failure
Zydus Pharmaceuticals is recalling 9,504 bottles of 2 mg risperidone tablets because they failed impurity specifications. The affected lot is MP4967.
Product
risperiDONE ORALLY DISINTEGRATING TABLETS, 2 mg, 30 Ct Bottles, Rx Only. Manufactured by: Cadila Healthcare Ltd., Ahmedabad, India. Distributed by: Zydus Pharmaceuticals USA Inc. Pennington, NJ 08534. NDC: 68382-156-06.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0727-2016·2016-03-02
Hospira Recalls Normosol-M Bags With Incorrect Expiration Date Labeling
Hospira is recalling 10,778 bags of Normosol-M and 5% Dextrose Injection due to an incorrect expiration date printed on the primary container.
Product
Normosol-M and 5% Dextrose (multiple electrolytes and 5% dextrose) Injection Type 1, USP, 1000 mL Single-Dose Container bag, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7965-09, Barcode (01) 0 030409 796509 0.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0728-2016·2016-03-02
Isomeric Pharmacy Recalls Triamcinolone Diacetate Injectable Suspension Due to Labeling Errors
Isomeric Pharmacy Solution, LLC is recalling 114 vials of Triamcinolone Diacetate Injectable Suspension because some vials may have incorrect lot numbers or expiration dates.
Product
Triamcinolone Diacetate Injectable Suspension, 40 mg/mL, 10mL Multi-Dose Vial for Injection, Rx only, Isomeric Pharmacy Solutions, 2401 Foothill Dr., Salt Lake City, UT 84109
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0672-2016·2016-02-24
Rhino 7 3000 Recalled for Undeclared Active Pharmaceutical Ingredients
Premiere Sales Group is recalling Rhino 7 3000 bottles because they contain undeclared active pharmaceutical ingredients, desmethyl carbondenafil and dapoxetine.
Product
Rhino 7 3000, 6 count Bottle, Distributed by Rhino 7, Made in USA
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0674-2016·2016-02-24
Medisca Recalls L-Citrulline API Due to Labeling Error
Medisca Inc is recalling L-Citrulline API bottles because FDA testing found the product contained N-acetyl-leucine instead of the labeled ingredient.
Product
CITRULLINE (L) in 25 g, 100 g, 500 g and 1 kg plastic bottles, White crystals or crystalline powder, odorless, For Use and distribution in prescription compounding, manufacturing, processing, or repackaging only in accordance with FDA regulations and applicable law, Packaged by…
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0671-2016·2016-02-24
Rhino 7 Platinum 3000 Recalled for Undeclared Active Ingredients
MSNV, Inc dba National Video Supply is recalling Rhino 7 Platinum 3000 single blister packs because they contain undeclared active pharmaceutical ingredients.
Product
Rhino 7 Platinum 3000, Single Blister Packs, distributed By Rhino 7, Made in USA
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0669-2016·2016-02-24
Glades Drugs Recalls Vitamin D3 Supplement Due to Excessive Potency
Glades Drugs Inc. is recalling Vitamin D3 supplement capsules because they contain an extremely high level of vitamin D3.
Product
Vitamin Supplement (Vial) D3, (cholecalciferol (vit D3)/lipoic acid/ubiquinol/ methylcobalamin/pyridoxine/methionine/inositol/choline bitartrate USP) capsules, 60, 120 or 180 count vials, Glades Drugs, 109 S. Lake Ave., Pahokee, FL 33476.
Category
Drug
Distribution
2 states
CriticalFDA (Drugs)·D-724-2016·2016-02-24
Pharmedium Recalls Subpotent Fentanyl Citrate Syringes for IV Use
Pharmedium Services, LLC is recalling 500 syringes of fentanyl citrate because the drug was subpotent. The affected product was distributed to nine hospital pharmacies.
Product
fentaNYL Citrate, Preservative Free, 10 mcg per 1 mL In 0.9% Sodium Chloride, 1 mL Total Volume For IV Use, packaged in a 3 mL syringe, code 2R3174, PharMEDium
Category
Drug
Distribution
7 states
CriticalFDA (Drugs)·D-0667-2016·2016-02-24
APEXXX tablets recalled for containing unapproved sildenafil
Nuway Distributors is recalling APEXXX tablets because they contain sildenafil, an unapproved drug for erectile dysfunction.
Product
APEXXX tablets, 300 mg, packaged in 1-count blister cards, Distributed Exclusively by: Nuway Distributors, LLC, Orlando, FL USA; UPC 7 05105 96361 7.
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0664-2016·2016-02-24
Akttive Fat Burner Recalled for Undeclared Dangerous Ingredients
Life and More LLC is recalling Akttive High Performance Fat Burner Gold capsules because FDA testing found undeclared sibutramine, desmethylsibutramine, and phenolphthalein.
Product
Akttive High Performance Fat Burner Gold dietary supplement capsules, 30-count bottle, Distributed by Life and More, L.L.C., Doral, Florida
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0673-2016·2016-02-24
Rhino 7 Platinum 3000 Recalled for Undeclared Active Ingredients
FDA recalls Rhino 7 Platinum 3000 because it contains undeclared active pharmaceutical ingredients, desmethyl carbondenafil and dapoxetine.
Product
Rhino 7 Platinum 3000, 1 count Blister Pack, Distributed by Rhino 7, Made in USA
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-723-2016·2016-02-24
Pharmedium Recalls Subpotent Fentanyl Citrate Syringes for IV Use
Pharmedium Services, LLC is recalling 180 syringes of fentanyl citrate because the drug was subpotent. The affected product was distributed to nine hospital pharmacies.
Product
fentaNYL Citrate, Preservative Free, 5 mcg per mL In 0.9% Sodium Chloride, 1 mL Total Volume For IV Use, packaged in a 3 mL syringe, code 2R3479, PharMEDium.
Category
Drug
Distribution
7 states
CriticalFDA (Drugs)·D-0662-2016·2016-02-24
Medline Recalls Mislabeled Acetaminophen Extra-Strength Pain Reliever Tablets
Medline Industries is recalling 500 mg acetaminophen tablets mislabeled as 325 mg. Consumers should stop using the product and return it to the retailer.
Product
ACETAMINOPHEN EXTRA-STRENGTH PAIN RELIEVER tablets, 500 mg, 100-count bottle, Distributed by Medline Industries, Inc., Mundelein, ILL 60060, NDC 53329-641-30.
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0675-2016·2016-02-24
Inaffit Recalls Natureal Burn Fat Nature Due to Undeclared Sibutramine
Inaffit, LLC is recalling Natureal Burn Fat Nature capsules because the product contains undeclared sibutramine and was marketed without an approved NDA or ANDA.
Product
NATUREAL BURN FAT NATURE, 30-count capsules, packaged in clear plastic bottle, Manufactured for: Inaffit, LLC. P.O. Box 34056, Bethesda, MD 20827.
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0722-2016·2016-02-24
Fit Firm and Fabulous Recalls Ultimate Herbal Slimcap Capsules
Fit Firm and Fabulous is recalling Ultimate Herbal Slimcap Capsules because they contain undeclared sibutramine, a controlled substance removed from the U.S. market for safety reasons.
Product
Ultimate Herbal Slimcap Capsules, 350 mg*, 30-count bottles, labeled Part 1 of 3, fit firm & fabulous, UPC 5 42423 25422 1.
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0668-2016·2016-02-24
Hospira Recalls Magnesium Sulfate Injection Bags Due to Incorrect Barcode Labeling
Hospira is recalling 213,600 bags of Magnesium Sulfate in Water for Injection because the primary bag labeling may be mislabeled with a barcode that scans as heparin sodium.
Product
MAGNESIUM SULFATE IN WATER — MAGNESIUM SULFATE IN WATER (MAGNESIUM SULFATE IN WATER)
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0670-2016·2016-02-24
Rhino 7 3000 Recalled for Undeclared Active Pharmaceutical Ingredients
MSNV, Inc dba National Video Supply is recalling Rhino 7 3000 bottles because they contain undeclared active pharmaceutical ingredients.
Product
Rhino 7 3000, 6 count bottles, Distributed by Rhino 7, Made in USA.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0699-2016·2016-02-24
Abbott's Compounding Pharmacy Recalls Sterile Compounded Products Due to Sterility Concerns
Abbott's Compounding Pharmacy is recalling all unexpired lots of sterile compounded products after an FDA inspection identified concerns regarding the lack of sterility assurance.
Product
papaverine phentolamine prostaglandin; 22.5/0.83 mg/15 mcg/mL; 5 mL unit size, refrigerate, This Rx is Compounded, Abbott's Compounding Pharmacy, Berkeley, CA 94705
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-0702-2016·2016-02-24
Abbott's Compounding Pharmacy Recalls Sterile Compounded Products for Sterility Concerns
Abbott's Compounding Pharmacy is recalling all unexpired lots of sterile compounded products, including papaverine phentolamine prostaglandin, due to FDA inspection findings regarding lack of sterility assurance.
Product
papaverine phentolamine prostaglandin; 25/1.5 mg/15 mcg/mL; 10 mL unit size, refrigerate, This Rx is Compounded, Abbott's Compounding Pharmacy, Berkeley, CA 94705
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-0692-2016·2016-02-24
Abbott's Compounding Pharmacy Recalls Sterile Compounded Products for Sterility Concerns
Abbott's Compounding Pharmacy is recalling all unexpired lots of sterile compounded products, including papaverine phentolamine prostaglandin, due to FDA inspection findings regarding lack of sterility assurance.
Product
papaverine phentolamine prostaglandin; 12/0.83 mg/10 mcg/ml; 5 mL and 10 mL unit size; refrigerate, This Rx is Compounded, Abbott's Compounding Pharmacy, Berkeley, CA 94705
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-0701-2016·2016-02-24
Abbott's Compounding Pharmacy Recalls Sterile Compounded Products for Sterility Concerns
Abbott's Compounding Pharmacy is recalling all unexpired lots of sterile compounded products after FDA inspection found concerns regarding lack of sterility assurance.
Product
papaverine phentolamine prostaglandin; 25/0.83 mg/20 mcg/mL; 5 mL and 10 mL unit sizes, refrigerate, This Rx is Compounded, Abbott's Compounding Pharmacy, Berkeley, CA 94705
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-0705-2016·2016-02-24
Abbott's Compounding Pharmacy Recalls Sterile Compounded Products for Sterility Concerns
Abbott's Compounding Pharmacy is recalling all unexpired lots of sterile compounded products containing papaverine, phentolamine, and prostaglandin due to FDA inspection findings regarding sterility assurance.
Product
papaverine phentolamine prostaglandin; 30/1 mg/10 mcg/mL; 5 mL, 7 mL and 10 mL unit sizes, refrigerate, This Rx is Compounded, Abbott's Compounding Pharmacy, Berkeley, CA 94705
Category
Drug
Distribution
1 state
SevereFDA (Drugs)·D-0706-2016·2016-02-24
Abbott's Compounding Pharmacy Recalls Sterile Compounded Products Due to Sterility Concerns
Abbott's Compounding Pharmacy is recalling all unexpired lots of sterile compounded products after FDA inspection found concerns regarding the assurance of sterility.
Product
papaverine phentolamine prostaglandin; 30/1 mg/20 mcg/mL; 5 mL unit size, refrigerate, This Rx is Compounded, Abbott's Compounding Pharmacy, Berkeley, CA 94705
Category
Drug
Distribution
1 state

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12226–12250 of 17785