Recall data checked 14 hours ago

Loading recalls…

Loading…

The Recall Registry is not a government service and does not issue recalls. We gather published recall notices from the U.S. Consumer Product Safety Commission, the U.S. Food and Drug Administration and the National Highway Traffic Safety Administration, and rewrite them in plain language. Always confirm the details with the issuing agency using the link on each recall page.

Home All recalls Services For shops For families Your account About Privacy Terms CPSC FDA NHTSA

Home › All recalls › Over-the-counter & supplements

Over-the-counter & supplements recalls

Pain relief, cold remedies, vitamins, dietary supplements.

Search recalls by product, brand or category

Or try another category

Everything

Children

Sleep & nursery280 Car seats254 Formula & baby food232 Children's medicine178 Swings & bouncers126 Nursery furniture324 Toys & play867 Strollers & carriers156 Clothing & sleepwear633

Adults & seniors

Prescription medicine2,102 Over-the-counter & supplements425 Mobility & home health186

Food & drink

Family food1,442

Pets

Pet food & products16

Home & car

Cleaning & chemicals273 Appliances & tools1,404 Furniture & furnishings580 Cars & vehicles12,377 Everything else2,332

Highest riskSeriousWorth checkingLabelling issueTap any recall for the hazard and what to do

425 recalls · newest first

Food & drug recall · FDASeptember 1, 2023Serious

AMMAN PHARMACEUTICAL INDUSTRIES — TRP Natural Eyes, Twitching Relief, Sterile Eye Ointment, Homeopathic 0.33 FL OZ (10 mL)

Over-the-counter & supplements · AMMAN PHARMACEUTICAL INDUSTRIES · 8,819 affected

Lack of Assurance of Sterility

Food & drug recall · FDAAugust 26, 2023Serious

Dr. Berne's Whole Health Products — Dr. Berne's Organic Castor Oil Eye Drops, Net WT 30 mL/1 fl oz bottle

Over-the-counter & supplements · Dr. Berne's Whole Health Products · 1744 bottles affected

CGMP Deviations

Food & drug recall · FDAAugust 18, 2023Serious

HUMANRACE — Humanrace Suncare, Ozone Body Protection Cream, Broad Spectrum Sunscreen SPF 30, packaged as a 148mL (5 fl oz.) bottle, PA ++++, 100% mineral, Active Ingredient: Zinc oxide 15%, Snow Mushroom, Squalene, Aloe, Dist. By: @Humanrac

Over-the-counter & supplements · HUMANRACE · 2942 units affected

Subpotent Drug: Product does not contain SPF that is declared on the label.

Food & drug recall · FDAAugust 18, 2023Serious

HUMANRACE — Humanrace Suncare, Ozone Face Protection Daily Moisturizer, Broad Spectrum Sunscreen SPF 30, packaged as a 53mL (1.8 fl oz.) bottle, 100% mineral, Active Ingredient: Zinc oxide 15%, Snow Mushroom, Dist. By: @Humanrace 2022 Bever

Over-the-counter & supplements · HUMANRACE · 5046 units affected

Subpotent Drug: Product does not contain SPF that is declared on the label.

Food & drug recall · FDAAugust 14, 2023Serious

Inmar Supply Chain Solutions, LLC — All Over-The-Counter (OTC) drug products warehoused, salvaged, and sold by Inmar.

Over-the-counter & supplements · Inmar Supply Chain Solutions, LLC · Unknown affected

CGMP Deviations: Potential exposure to rodents and rodent activity in the distribution center.

Food & drug recall · FDAAugust 11, 2023Serious

AVKARE LLC — Sodium Fluoride 1.1%, SODIUM FLUORIDE Prescription Dental Toothpaste, 5000 ppm Fluoride Plus Mild Cleaning System Spearmint NET WT. 1.8 OZ. (51g), Rx only, NDC 42291-741-51

Over-the-counter & supplements · AVKARE LLC · 35,184 tubes affected

Cases of Sodium Fluoride 1.1% Prescription Dental Toothpaste may contain cartons labeled as Capsaicin Cream 0.025% but contain correctly labeled…

Food & drug recall · FDAAugust 11, 2023Serious

AVKARE LLC — Capsaicin Cream 0.025%, External Analgesic Cream, Penetrating Pain Relief, NET WT. 2.1 OZ. (60g) NDC 50268-195-60

Over-the-counter & supplements · AVKARE LLC · 35,184 cartons affected

Product mix-up: Cartons labeled Capsaicin Cream 0.025% may contain tubes of Sodium Fluoride 1.1% Prescription Dental Toothpaste

Food & drug recall · FDAAugust 10, 2023Serious

Colgate Palmolive Company — hello wild strawberry fluoride toothpaste, sodium fluoride 0.24% (0.15% w/v fluoride ion), NET WT 4.2 OZ (119 g)

Over-the-counter & supplements · Colgate Palmolive Company · 182,046 tubes affected

Labeling: Label Mix-Up: Some hello wild strawberry fluoride toothpaste, packaged in cartons labeled as hello wild strawberry fluoride toothpaste were…

Food & drug recall · FDAAugust 9, 2023Serious

Ecometics, Inc. — Unguentine Ointment, (Camphor 3.0%, Phenol 2.5%, Tannic Acid 2.2%, Zinc Oxide 6.6%), labeled as a) NET WT 1 OZ (28 g) tubes, Improved Formula, UPC 0 11169 10216 0, and b) NET WT 1 OZ (28.3g) tubes, Maximum Strength, UPC 0

Over-the-counter & supplements · Ecometics, Inc. · a) 6,120 tubes, b) 540 tubes affected

CGMP Deviations: Products not manufactured under current good manufacturing practices.

Food & drug recall · FDAAugust 2, 2023Serious

Parker Laboratories, Inc. — Protex Foaming Hand Sanitizer (Benzalkonium Chloride 0.13%), packaged in a) 2 fl oz/60 mL Pump bottles (NDC 30775-040-02) and b)18 fl. oz./550 ml Pump Bottles (NDC 30775-040-18), Parker Laboratories, Inc. 286 Eld

Over-the-counter & supplements · Parker Laboratories, Inc. · 9 affected

CGMP Deviations

Food & drug recall · FDAApril 26, 2023Highest risk

Gadget Island, Inc — Pro Power Knight Plus capsule, 2550mg, 1-count blister card

Over-the-counter & supplements · Gadget Island, Inc · 628 blister cards affected

Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with undeclared sildenafil and tadalafil, ingredients found in FDA…

Why this is here: It was found to contain a drug or chemical that is not on the label. That is different from an allergen or a contamination scare: anyone taking it has been taking a substance nobody prescribed, in an unknown dose, and it can interact with medication they are already on. Follow the agency notice rather than judging it by how the product looks.

Food & drug recall · FDADecember 2, 2022Serious