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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.

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Over-the-counter & supplements recalls

Pain relief, cold remedies, vitamins, dietary supplements.

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Children

Sleep & nursery274 Car seats254 Formula & baby food230 Children's medicine176 Swings & bouncers125 Nursery furniture317 Toys & play852 Strollers & carriers156 Clothing & sleepwear626

Adults & seniors

Prescription medicine1,991 Over-the-counter & supplements377 Mobility & home health182

Food & drink

Family food1,229

Pets

Pet food & products15

Home & car

Cleaning & chemicals271 Appliances & tools1,380 Furniture & furnishings572 Cars & vehicles12,229 Everything else2,312

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

377 recalls · newest first

Food & drug recall · FDAOctober 31, 2025Serious

Blossom Pharmaceuticals — Nivagen, Zinc Oxide Ointment, Net Wt. 1 oz. (28.4g), Nivagen Pharmaceuticals, Inc., Sacramento, CA 95827, USA Made in India, NDC 75834-170-01.

Over-the-counter & supplements · Blossom Pharmaceuticals · 13536 containers affected

cGMP deviations

Food & drug recall · FDAOctober 31, 2025Serious

Blossom Pharmaceuticals — Nivagen, Zinc Oxide Ointment USP, Zinc Oxide 20 %, Net Wt. 1 oz. (28.4g), Nivagen Pharmaceuticals, Inc., Sacramento, CA 95827, USA, Made in India, NDC 75834-170-02.

Over-the-counter & supplements · Blossom Pharmaceuticals · 7920 bottles affected

cGMP deviations

Food & drug recall · FDAOctober 31, 2025Serious

Blossom Pharmaceuticals — WeCare, Zinc Oxide Ointment, Net Wt. 15 oz/425 g, Manuactured for: Dynarex Corporation, 11 Dynarex Drive, Middletown, NY 10941, Made in India, NDC 67777-223-05.

Over-the-counter & supplements · Blossom Pharmaceuticals · 2592 bottles affected

cGMP deviations

Food & drug recall · FDAOctober 21, 2025Serious

Kenvue Brands LLC — TYLENOL, Acetaminophen, Extra Strength, 24 Caplets, 500mg each

Over-the-counter & supplements · Kenvue Brands LLC · 3,816 bottles affected

Defective Container

Food & drug recall · FDAOctober 17, 2025Serious

Aero Healthcare — Acetaminophen 500mg Caffeine 65mg caplets, packaged as 2 caplets per packet further packaged in a 50-count box, AERO TAB

Over-the-counter & supplements · Aero Healthcare · N/A affected

Labeling: Label Mix-up.

Food & drug recall · FDAOctober 10, 2025Serious

CA BOTANA International, Inc. — Sugared+Bronzed Tinted Mineral Sunscreen SPF 50, Zinc Oxide 21%, Net WT 3.3 OZ (93 G) per tube, Dist. By: Sugared+Bronzed, 929 Montana Ave, Santa Monica, CA 90403. NDC: 35192-055-18, UPC 8 50047 92223 6

Over-the-counter & supplements · CA BOTANA International, Inc. · 2090 tubes affected

CGMP Deviations

Food & drug recall · FDAOctober 10, 2025Serious

CA BOTANA International, Inc. — Doctor. D. Schwab Mineral Sunscreen SPF 50, Zinc Oxide 21%, 4 oz./ 113.4 g per tube

Over-the-counter & supplements · CA BOTANA International, Inc. · 1167 tubes affected

CGMP Deviations

Food & drug recall · FDAOctober 10, 2025Serious

CA BOTANA International, Inc. — Elixir by Coco March Mineral Sunscreen SPF 50, Zinc Oxide 21%, 2.1 oz (62g) per bottle

Over-the-counter & supplements · CA BOTANA International, Inc. · 3295 bottles affected

CGMP Deviations

Food & drug recall · FDAOctober 10, 2025Serious

CA BOTANA International, Inc. — Doctor D. Schwab Shimmery Sun Lotion Sunscreen SPF 30, Titanium Dioxide 5% and Octinoxate 4%, 4 oz./113.4 g per tube, Doctor D. Schwab, A division of CA BOTANA, San Diego, CA 92121. NDC: 35192-012-02

Over-the-counter & supplements · CA BOTANA International, Inc. · 805 tubes affected

CGMP Deviations

Food & drug recall · FDAOctober 10, 2025Serious

CA BOTANA International, Inc. — Gabriel Mineral Sunscreen SPF 50, Zinc Oxide 21%, 2.1 oz, Net 61 g per tube, Dist. By: Gabriel Cosmetics, Inc., Redmond, WA USA 98052, NDC: 35192-044-01, UPC 7 07060 9592 1

Over-the-counter & supplements · CA BOTANA International, Inc. · 1617 tubes affected

CGMP Deviations

Food & drug recall · FDAOctober 10, 2025Serious

CA BOTANA International, Inc. — Sea Enzyme Ultra Umbrella Sunscreen SPF 30, Titanium Dioxide 4%, Octinoxate 4%, 4 oz./113.4 g per tube

Over-the-counter & supplements · CA BOTANA International, Inc. · 874 tubes affected

CGMP Deviations

Food & drug recall · FDAOctober 10, 2025Serious

CA BOTANA International, Inc. — Elixir by Coco March Tinted Mineral Sunscreen SPF 50, Zinc Oxide 21%, 2.1 oz (62g) per bottle

Over-the-counter & supplements · CA BOTANA International, Inc. · N/A affected

CGMP Deviations

Food & drug recall · FDAOctober 8, 2025Highest risk

Mohamed Hagar — Mojo Max Fusion XXX, 500 mg, one capsule per blister card, 20 count box

Over-the-counter & supplements · Mohamed Hagar · 125 boxes affected

Marketed Without an Approved NDA/ANDA-FDA analysis revealed undeclared sildenafil (13.1 mg/capsule) and tadalafil (13.8 mg/capsule).

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 · FDASeptember 29, 2025Highest risk

Acuity Specialty Products, Inc. — Wyandotte, Sanifect E3, Hand Sanitizer (Ethanol-Based, Product 5511), Ethyl Alcohol 60.1%, Manufacture By: AFCO, 550 Development Avenue, Chambersburg, PA 17210, Toll Free: 800-345-1329, Package Configuratio

Over-the-counter & supplements · Acuity Specialty Products, Inc.

cGMP deviations: The recall was initiated because required receipt testing of incoming alcohol components used to manufacture the listed hand…

Food & drug recall · FDASeptember 29, 2025Highest risk

Acuity Specialty Products, Inc. — AFCO, Hand Sanitizer (Isopropyl Alcohol-Based, Product 5515)

Over-the-counter & supplements · Acuity Specialty Products, Inc.

cGMP deviations: The recall was initiated because required receipt testing of incoming alcohol components used to manufacture the listed hand…

Food & drug recall · FDASeptember 25, 2025Serious

SV Labs Prescott Corporation — Aloe Up Sport Performance Sunscreen Lotion SPF 30, 1 FL OZ (30 mL) per tube, Mfd. for: ALOE UP, 9700 W. 76th St., Ste 112, Eden Prairie, Minnesota 55344

Over-the-counter & supplements · SV Labs Prescott Corporation · 11,386 tubes affected

cGMP deviations: the firm released and distributed product which failed total aerobic microbial count testing.

Food & drug recall · FDAAugust 27, 2025Serious

DermaRite Industries, LLC — PeriGuard Ointment, Petrolatum 49.9%, packaged in a) 5g (NDC 61924-205-05), b) 3.5oz (NDC 61924-205-04), and c) 7oz (NDC 61924-205-07) tubes, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 0704

Over-the-counter & supplements · DermaRite Industries, LLC · 381,619 units affected

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

Food & drug recall · FDAAugust 27, 2025Serious

DermaRite Industries, LLC — DermaKleen, Health Care Antiseptic Lotion Soap with Vitamin E, Chloroxylenol 0.2%, packaged in a) 222 mL (7.5 fl. oz.) per tube (NDC 61924-092-08), b) 800 mL (27 fl. oz.) per bag (NDC 61924-092-27), and c 1000 mL

Over-the-counter & supplements · DermaRite Industries, LLC · 7,736 tubes affected

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

Food & drug recall · FDAAugust 27, 2025Serious

DermaRite Industries, LLC — GelRite Instant Hand Sanitizer, Alcohol 65%, packaged in a) 118 mL (NDC 61924-106-04), b) 473 mL (NDC 61924-106-16) and c) 800 mL (NDC 61924-106-27), and d) 1000 mL (NDC 61924-106-34) per container, DermaRite Ind

Over-the-counter & supplements · DermaRite Industries, LLC · 115,994 containers affected

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

Food & drug recall · FDAAugust 27, 2025Serious

DermaRite Industries, LLC — DermaMed Ointment, Skin Protectant, Aluminum Hydroxide Gel 2%, Net Wt. 106 g (3.75 oz.) per tube, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-214-04

Over-the-counter & supplements · DermaRite Industries, LLC · 2,673 tubes affected

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

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