1,320 recalls tagged with “fda regulated”.
ZOLIQUEX recalled adult portable bed rails sold on Amazon after reports of entrapment and asphyxiation risk. The recall targets silver bed rails measuring 12.4 inches wide by 33.07 inches tall and weighing 7.1 pounds. The model numbers ZEX014-V1 and the Zoliquex branding appear on packaging. Stop using the product and seek a full refund by contacting ZOLIQUEX.
Fengrong Tool recalls electric pressure washers sold under the Fengrong brand due to lack of a ground-fault circuit-interrupter. The recall affects products described as orange or green with black and a touch screen, about 25.5 inches tall, 12 inches wide and 11 inches deep. Units were labeled “High pressure washer.” Consumers should stop using the product and seek a full refund by contacting feng
ATOYUS recalled its wooden activity cubes after authorities identified a choking hazard from spherical mallet ends and detached xylophone screws and clock hands. The recall covers products sold on Amazon by Melofaver US. Consumers should stop using the toy immediately and return it for a full refund.
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
Fun and Function recalled MW7661 multi-point swing frames due to crack and break risk. The frames were sold online by Funandfunction.com from May 2022 through February 2026 for $200-$250. Consumers should stop using the product immediately and contact the company for a full refund.
Silks recalled all children's two-piece loungewear sets sold online at Silksdesign.com. These sets violate mandatory flammability standards for children's sleepwear and pose a serious burn risk. Parents should stop using the recalled loungewear immediately and contact Silks for a full refund or store credit.
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.
Coluans recalled Christmas Light-Up Rings sold on Amazon by BUDI Official. The recall centers on a battery ingestion hazard from three preinstalled button cell batteries visible through the ring’s clear casing. Stop using the rings immediately and return them for a full refund by emailing BUDIrecall@outlook.com with a photo of the disposed product.
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
K.C. Pharmaceuticals recalled eight OTC eye drops sold nationwide under CVS Health, Walgreens and Kroger brands after sterility could not be verified. The recall covers all lots within expiry through Oct 31, 2026. Nonsterile eye drops can harbor bacteria and fungus, causing serious infections that may lead to vision loss. Stop using recalled products and return them for a full refund at the store.
House of Flavors recalled 4,880 tubs of Chicago Vanilla Naturally Flavored Ice Cream, 3 GAL tub, distributed in Illinois. The product contains undeclared egg. Consumers should not consume it and should contact House of Flavors for refund or replacement via email.
HEYTEA USA INC recalls 12,677 cartons of Coconut Drink 1 sold for catering establishments in multiple states after undeclared milk was found. The product contains milk not listed on the label. Consumers should not consume the product and contact HEYTEA USA INC for refund or replacement by email.
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 28,157 bottles of PRAZOSIN HYDROCHLORIDE capsules, distributed nationwide in the USA. The recall cites cGMP deviation due to detection of N-nitroso-prazosin impurity C above acceptable limits. Stop using the product immediately and contact Appco Pharma LLC or your 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‑
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.