1,079 recalls tagged with “chemical hazard”.
BMW recalls 2025-2026 X1 and X2 models plus MINI Cooper and Countryman variants for front seat belt retractors with damaged torsion bars. The defect may fail to restrain occupants in a crash. Dealers will replace both front retractors at no cost. Owner letters begin November 7, 2025. VIN lookup will be available on NHTSA.gov the same day.
Sanlebi Pet Vet Playsets, sold on Amazon by Letokids, are recalled after reports of accessible button cell batteries in the nail grinder and otoscope. The recall affects model MX094. Consumers should remove the nail grinder and otoscope components and seek a refund or replacement. Disposed components must be photographed and emailed for the refund process.
ZMC Group recalls LED Finger Beam Lights, model A10-8, sold at discount stores nationwide from August 2025 through March 2026 for about $1. The recall is active as of April 16, 2026. The toy contains three pre-installed AG3 button cell batteries that can be accessed by children. Consumers should stop using the lights and seek a full refund or replacement. Contact ZMC Group for instructions and to
Vitaquest International recalled Arey Not Today iron supplements sold at retailers nationwide after determining the products do not meet the Poison Prevention Packaging Act's child-resistant packaging requirement. The noncompliant packaging creates a poisoning risk to young children if ingested. Consumers should stop using the products immediately and contact Vitaquest for a free child-resistant替换
Head USA recalls ski boots with fluorescent yellow components from 2016–2022 model years. The recall covers boots and inserts with six-digit article codes. Consumers should stop using recalled boots immediately and contact Head for a free replacement or sole-insert option.
BISSELL recalled more than 1 million Steam Shot OmniReach handheld steam cleaners with attachments, sold nationwide through retailers. The attachments can detach and expel hot water or steam, posing a serious burn hazard. Stop using the attachments immediately and contact BISSELL to receive free replacement attachments.
Taro Pharmaceuticals announced a market withdrawal of Diclofenac Sodium, Topical Gel, 3% on January 27, 2026. The withdrawal stems from out of specification viscosity results. Healthcare providers and consumers should stop using the product immediately.
Sangohe expands its 2026 recall of adult portable bed rails 504E and 504Q due to entrapment and asphyxiation risk. The recall cites noncompliance with the mandatory standard and missing warning labels. Stop using the recalled rails and pursue a full refund by contacting Sangohe.
Sam's Club recalls Member's Mark Valentine pajama sets due to burn risk and a violation of mandatory flammability standards for children's sleepwear. The recall covers sizes XS through XL sold online between December 2025 and January 2026 for about $14. Consumers should stop using the pajamas immediately and contact Sam's Club for a full refund.
F&S Fresh Foods recalled 325 ReadyMeals Turkey Bacon & Cheddar Pretzel Duo Sandwiches distributed in Oregon after sesame was not declared on the label. The issue involves sesame as an undeclared allergen in a product labeled to contain egg, milk, soy, and wheat. Consumers should not eat the sandwich and should contact F&S Fresh Foods for refunds or replacements.
Tuymec Minoxidil Hair Growth Kit sold on Amazon by DrHealBeauty is recalled for non-child-resistant packaging. The kit contains two black spray bottles with 5% minoxidil and BIOTIN labels. Consumers should stop using the product immediately and contact DrHealBeauty for a free empty replacement bottle with a child-resistant closure.
TecFlox recalled its Minoxidil Topical Solution hair growth serum bottles on April 2, 2026. The packaging is not child-resistant, violating the Poison Prevention Packaging Act. Consumers should stop using the product immediately, store it out of reach of children, and email TecFloxrecall@outlook.com to receive free replacement bottles. Only bottles with serum remaining will be replaced; dispose of
Biocon Pharma Inc. recalled 88,008 bottles of Prazosin Hydrochloride capsules, 1 mg, 100-count bottles, nationwide in the United States. A cGMP deviation detected N-nitroso-prazosin impurity C above acceptable limits. Consumers and healthcare providers should stop using this product immediately and contact Appco Pharma LLC or a healthcare provider for guidance.
Biocon Pharma Inc. recalled 58,896 bottles of Prazosin Hydrochloride Capsules, USP, 2 mg, 100-count bottle. The product was distributed nationwide in the USA and manufactured by Appco Pharma LLC. A cGMP deviation detected N-nitroso-prazosin impurity C above acceptable limits. Consumers and healthcare providers should stop using this product immediately and contact Appco Pharma LLC or their health‑
Blueroot Health recalled Aller-C dietary supplement bottles after discovering undeclared allergens. The recall covers Aller-C bottles in 100-count and 200-count sizes distributed across 35 states. Consumers should not consume the product and should seek refund or replacement.
Zarlengo Italian Ice recalls 173 one-gallon gelato buckets sold in Illinois, Indiana and Texas. Soy lecithin appears in ingredients but is not listed in the contains statement. Consumers should not consume this product and should seek refund or replacement.
Zarlengo Italian Ice recalls 1,333 units of Chocolate Chocolate Chip Gelato distributed in Illinois, Indiana and Texas after discovering a mismatch between ingredients and contains statements. Soy lecithin appears in the ingredients list but is not referenced in the contains statement. The recall is Class II with high hazard potential. Consumers should not consume the product and should seek a退款或替
Zarlengo Italian Ice recalled 757 units of chocolate gelato across multiple sizes in Illinois, Indiana and Texas. The issue centers on a soy lecithin omission in the contains statement. Consumers should not eat the product and should seek a refund or replacement.
Geri-Care eye drops recalled nationwide after lack of sterility assurance affects 720 bottles. The product, ARTIFICIAL TEARS with NDC 68788-7266-0, is manufactured by Preferred Pharmaceuticals, Inc. in Brooklyn, NY. The FDA recall class II points to a risk of contamination. Stop using immediately and contact a healthcare provider for guidance.
Connecticut Crab Company LLC recalls 39 boxes of crab cakes sold to food service due to potential temperature abuse that could enable Clostridium botulinum growth. The recall notice is active as of April 15, 2026. Consumers who purchased these products should not consume them and should seek refund or replacement information from the company.