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

1676–1700 of 17762

HighFDA (Drugs)·D-0489-2024·2024-05-15
TraMADol HCl 50 mg Tablets Recalled for Foreign Baclofen Tablets
RemedyRepack Inc. is recalling TraMADol HCl 50 mg tablets nationwide after a pharmacist discovered a baclofen tablet in a tramadol bottle. Taking the wrong medication poses serious health risks.
Product
TraMADol HCl 50 mg Tablet, Packaged as (a) 30-count blister pack, NDC 70518-3824-00; (b) 90-count blister pack, NDC 70518-3824-02; (a) 180-count blister pack, NDC 70518-3824-03; RX ONLY, MFG: Advagen Pharma Limited, Plainsboro. NJ 08536, Repackaged by: RemedyRepack Inc., Indiana,
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0490-2024·2024-05-15
Prescription skin cleanser recalled nationwide due to subpotency
Acella Pharmaceuticals recalled 7,104 bottles of Sodium Sulfacetamide 10% Sulfur 5% Cleanser nationwide because the product contained less active ingredient than labeled. The recall was terminated in December 2025.
Product
SODIUM SULFACETAMIDE 10 SULFUR 5 CLEANSER — SODIUM SULFACETAMIDE 10 SULFUR 5 CLEANSER (SULFACETAMIDE SODIUM AND SULFUR)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0492-2024·2024-05-15
Clorazepate Dipotassium Tablets Recalled for Tablet Discoloration Defects Nationwide
Aurobindo Pharma USA Inc. is recalling 6909 bottles of Clorazepate Dipotassium 7.5 mg tablets due to visible discoloration with yellow and dotted spots. No illnesses or injuries have been reported.
Product
CLORAZEPATE DIPOTASSIUM — CLORAZEPATE DIPOTASSIUM (CLORAZEPATE DIPOTASSIUM)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0491-2024·2024-05-15
Clorazepate Dipotassium Tablets Recalled Due to Cosmetic Discoloration
Aurobindo Pharma USA Inc. is recalling Clorazepate Dipotassium Tablets 3.75 mg due to yellow dots and discoloration on some tablets distributed nationwide.
Product
CLORAZEPATE DIPOTASSIUM — CLORAZEPATE DIPOTASSIUM (CLORAZEPATE DIPOTASSIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0477-2024·2024-05-08
Methylergonovine Maleate tablets recalled for failed dissolution specifications
Amneal Pharmaceuticals recalls Methylergonovine Maleate 0.2mg tablets nationwide due to failed dissolution specifications. The tablets may not dissolve properly, potentially reducing medication effectiveness.
Product
METHYLERGONOVINE MALEATE — METHYLERGONOVINE MALEATE (METHYLERGONOVINE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0476-2024·2024-05-08
FDA Issues Nationwide Recall of Subpotent Ophthalmic Eye Drops
The FDA is recalling 3,320 bottles of compounded ophthalmic solution due to subpotency. The affected product does not contain adequate amounts of active medication.
Product
Prednisolone Sodium Phosphate-Moxifloxacin-Bromfenac Sterile Ophthalmic Solution 1%, 0.5%, 0.075%, 8mL, Compounded By: Imprimis NJOF, LLC. 1705 Route 46 West, Unit 6B Ledgewood, NJ 07852, NDC 71384-340-08
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0479-2024·2024-05-08
EYLEA injection recalled for sterility concerns and syringe breakage complaints
Regeneron Pharmaceuticals recalled over 251,000 EYLEA (aflibercept) injection syringes distributed nationwide due to complaints of syringe breakage and concerns about sterility assurance in specific lots.
Product
EYLEA — EYLEA (AFLIBERCEPT)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0480-2024·2024-05-08
Fentanyl Injection Bags Recalled Due to Incorrect Barcode Labels
Hikma Injectables USA Inc. has recalled 1,895 bags of Fentanyl 1000mcg/100mL injection (lot CH0324001) due to incorrect barcodes on the product labeling.
Product
Fentanyl 1000mcg/100mL (10mcg/mL) in 0.9% Sodium Chloride Injection, packaged in 100mL bags, Rx only, Compounded by: Hikma Injectables USA Inc. 2 Esterbrook Lane, Cherry Hill, NJ 08003, Distributed by: Hikma Injectables USA Inc. 36 Stults Road, Dayton, NJ 08810, NDC 63037-100-05
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0481-2024·2024-05-08
Prescription Valacyclovir Tablets Recalled Due to Missing Imprint
Viatris Inc is recalling 143,230 bottles of Valacyclovir Hydrochloride 500 mg tablets due to missing imprints on some tablets. The recall is nationwide and affects two lot numbers expiring in June 2024 and May 2025.
Product
VALACYCLOVIR HYDROCHLORIDE — VALACYCLOVIR HYDROCHLORIDE (VALACYCLOVIR)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0478-2024·2024-05-08
Injectable epinephrine-lidocaine recalled for failing potency specification
Imprimis NJOF, LLC is recalling epinephrine-lidocaine injectables nationwide because they failed to meet potency specifications. Patients should contact their healthcare provider regarding affected lots.
Product
Epinephrine-Lidocaine HCl 0.25 mg/mL and 7.5 mg/mL Preservative-Free, 1 mL Single-Use vials, Rx only, Imprimis NJOF, LLC 1705 Route 46 West, Unit 6B, Ledgewood, NJ, 07852, NDC 71384-640-01
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0459-2024·2024-05-01
FDA Recalls Alcoholada Gel Pain Reliever Over Methanol Contamination
Alcoholada Gel pain reliever is being recalled because the ethanol ingredient contains methanol contamination. The FDA classified this as a Class I recall affecting 9,625 bottles distributed nationwide.
Product
Alcoholada Gel, Pain Relieving Gel, 0.5% Lidocaine Hydrochloride, packaged in (a) 8.5 fl oz (251 mL) plastic bottle UPC 0 82252 03120 9 (b) 2.2 fl oz (65 mL) plastic bottle, UPC 0 82252 34030 1 , Manufactured in Aruba by Aruba Aloe Balm Inc., Pitastraat 115, Aruba, Dutch Caribbe
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0455-2024·2024-05-01
Silverback XXX Power male enhancement product recalled for undeclared sildenafil and tadalafil
Pyramids Wholesale Inc. is recalling Silverback XXX Power male enhancement nationwide due to undeclared sildenafil and/or tadalafil. These prescription drugs were not approved by the FDA before marketing.
Product
SILVERBACK XXX POWER MALE ENHANCEMENT, 2 fl. oz., UPC 8 700470 032762
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0460-2024·2024-05-01
FDA Recalls Aruba Aloe Hand Sanitizer for Methanol Contamination
FDA is recalling 5,299 bottles of Aruba Aloe Hand Sanitizer Gel nationwide due to methanol contamination in the ethanol ingredient. Consumers should stop using the product immediately.
Product
Aruba Aloe Hand Sanitizer Gel, 80% Alcohol, 12 fl oz (355 mL) plastic bottle, Manufactured in Aruba by Aruba Aloe Balm Inc., Pitastraat 115, Aruba, Dutch Caribbean. UPC 0 82252 03300 5
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0452-2024·2024-05-01
Pink Pussycat Honey recalled for undeclared sildenafil and tadalafil content
Pyramids Wholesale Inc. is recalling Pink Pussycat Honey because it contains undeclared sildenafil and tadalafil and was marketed without FDA approval. The recall affects all lots nationwide.
Product
Pink Pussycat Honey, net wt: 20gx12 sachets, UPC 7 918750 046557
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0458-2024·2024-05-01
Sexual Enhancement Product Recalled for Undeclared Prescription Drugs
Pyramids Wholesale Inc. is recalling HONEY MANUKA BUNNY LOVE nationwide because it contains undeclared sildenafil and/or tadalafil—prescription medications—and was marketed without FDA approval.
Product
HONEY MANUKA BUNNY LOVE, 12g, All Natural Sexual Enhancement, UPC: N/A
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0449-2024·2024-05-01
Honey product recalled nationwide for undeclared sildenafil and tadalafil
Pyramids Wholesale Inc. is recalling Weiner Boner Honey due to undeclared sildenafil and tadalafil. The product was distributed nationwide without FDA approval.
Product
Weiner Boner Honey, 12g packet, 100% Organic Formula.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0450-2024·2024-05-01
FDA Recalls Flower Power Female Enhancement for Undeclared Sildenafil and Tadalafil
Flower Power CBD infused Female Enhancement contains undeclared sildenafil and tadalafil. These prescription drugs were not disclosed to consumers and the product was marketed without FDA approval.
Product
Flower Power, CBD infused Female Enhancement, 59 ml bottle, UPC 0 678741 351646.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0470-2024·2024-05-01
ForeverMen Natural Energy Boost Capsules Recalled for Undeclared Sildenafil
ForeverMen Natural Energy Boost Capsules contain undeclared sildenafil and are marketed without FDA approval, making them an unapproved drug. Consumers should stop using the product immediately.
Product
ForeverMen Natural Energy Boost Capsules, packaged in a box containing a 10-count blister card.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0456-2024·2024-05-01
The GOAT Sublingual Strip Recalled for Undeclared Prescription Drug Ingredients
The GOAT Sublingual Strip male enhancement product, distributed nationwide, was recalled for containing undeclared sildenafil and tadalafil. The product was marketed without FDA approval.
Product
The GOAT SUBLINGUAL STRIP, MALE ENHANCEMENT, 2 Pack, Distributed by Hombres LLC, 130 Maccormick Ave, Suite 105, Costa Mesa, A, UPC 6 61631 26363 1.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0454-2024·2024-05-01
FDA Recalls libigrow RED DRAGON+ Capsules for Undeclared Sildenafil and Tadalafil
Pyramids Wholesale Inc. is recalling libigrow RED DRAGON+ capsules nationwide because they contain undeclared sildenafil and tadalafil, prescription medications not approved by the FDA for this product.
Product
libigrow RED DRAGON+, Maximum Strength Formula, 2 capsules per box, UPC 7 05105 83073 5.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0448-2024·2024-05-01
Spanish Fly 22K Capsules Recalled for Undeclared Prescription Drug Ingredients
Spanish Fly 22K capsules contain undeclared sildenafil and/or tadalafil and were marketed without FDA approval. The product poses serious health risks from these unapproved pharmaceutical ingredients.
Product
Spanish Fly 22K capsules, 2-count box, UPC 0 664979 979455
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0451-2024·2024-05-01
Samurai-X Honey 6800 Recalled for Undeclared Drug Ingredients
Samurai-X Honey 6800, manufactured by Pyramids Wholesale Inc., is recalled for containing undeclared sildenafil and/or tadalafil. The product was distributed nationwide and marketed without FDA drug approval.
Product
Samurai-X Honey 6800, UPC 2 56891 27553 3.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0457-2024·2024-05-01
Male Performance Enhancer Recalled for Undeclared Sildenafil and Tadalafil
ALPHASTRIP Male Performance Enhancer strips are being recalled nationwide because they contain undeclared sildenafil and tadalafil. The product was marketed without FDA approval.
Product
ALPHASTRIP MALE PERFORMANCE ENHANCER, The fastest acting sublingual, Serving Size (1 strip), Distributed by: GALT INT'L
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0453-2024·2024-05-01
Male Sexual Enhancement Product Recalled for Undeclared Pharmaceutical Ingredients
Pyramids Wholesale Inc. is recalling all lots of GoHARD 25000 because it contains undeclared sildenafil and tadalafil. The product was marketed without FDA approval for these prescription-strength drugs.
Product
GoHARD 25000, Male Sexual Enhancement, Honey, 100% Natural, UPC: N/A.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0471-2024·2024-05-01
Prescription respiratory drug recalled for short fill in unit-dose vials
Cipla USA recalls Ipratropium Bromide and Albuterol Sulfate inhalation solution due to short fill in unit-dose vials. Some vials contain less medication than labeled, affecting dosage.
Product
IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE — IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE (IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE)
Category
Drug
Distribution
Distributed nationwide

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1676–1700 of 17762