613 recalls tagged with “poisoning risk”.
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.
JC Sales has issued an active recall for Lil' Buddies Pet Laser Toys, model 24496, sold by discount retailers nationwide. The recall cites serious injury or death risk from battery ingestion. The toys include three button cell batteries and fail to meet mandatory standards for teething toys.
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
Wybotics is recalling specific Osprey 700 Max and S1 robotic pool vacuums sold through retailers after reports that the lithium-ion battery can overheat, creating a burn and fire hazard. The recall covers Osprey 700 Max models WY3312MAX and WY100MAX and S1 WY200, with serial numbers WY100M230117XXXX, WY100M230127XXXX, WY100M230130XXXX, WY100M230318XXXX, WY200-230328XXXX and W200**230330XXXX. The U
Shenzhen Shijingjie Network Technology recalled two models of male-to-male extension cords sold at Walmart after safety concerns. The cords pose a risk of electrocution and carbon monoxide poisoning when used for backfeeding from a generator into a home. Consumers should stop using the recalled cords immediately and contact the company for a full refund.
Gavoyeat recalled 50-ring Halloween Light-Up Rings sold on Amazon by CSZWEICD on April 2, 2026. The recall cites a battery ingestion hazard from an accessible button cell battery in the ring’s housing. Stop using the recalled rings and return them for a full refund by emailing recalledgavoyeat@yeah.net.
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
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‑
GLMZZ recalled magnet ball toy sets after magnets posed a ingestion risk. The recall notice does not specify a retailer. The hazard is high-powered magnets that can injure or kill if swallowed. Stop using the recalled product and contact GLMZZ for a full refund.
Lily's Bakery Factory recalls 890 boxes of Cuban Crackers Galletas Cubanas sold in Florida due to undeclared color additives. FD&C Yellow 5, Yellow 6 and Red 40 are not listed on the label. Consumers should not eat the product and should seek a refund or replacement from the company.
Fagron Compounding Services recalled 34,260 bags of Vancomycin HCI Injection across the United States. The recall cites lack of sterility assurance and a blue Break-Off-Part that could detach from the administration port. Healthcare providers and patients should stop using the product immediately and follow manufacturer guidance.
Fagron Compounding Services is recalling 11,680 bags of Vancomycin HCl 1 g in 250 mL 0.9% Sodium Chloride Injection. The recall is nationwide in the United States. The blue break-off part could detach from the administration port, raising sterility concerns. Stop using immediately and contact the provider for guidance.
Teva-affiliated Clonidine Transdermal System recalls 113,943 cartons after CGMP deviations. Unapproved raw material prompts recall. Stop use immediately and contact Teva or a healthcare provider for guidance.
Amneal Pharmaceuticals is recalling 29,542 bottles of TRAMADOL HYDROCHLORIDE tablets distributed nationwide in the United States. The recall cites a failed impurity specification for N-nitroso-desmethyl-tramadol (NDSRI) at the 24‑month stability interval. Consumers and healthcare providers should stop using the product immediately and contact Amneal for guidance.
Riverence Provisions LLC recalls 3,672 units of Smoked Trout Dip sold frozen in cases distributed to eight states over milk allergen labeling. The recall is active as of April 15, 2026. Do not consume the product. Contact Riverence Provisions for refund or replacement.
Teva Pharmaceuticals recalled 124,054 cartons of Clonidine Transdermal System due to CGMP deviations from an unapproved raw material. The recall affects products sold in the United States. Consumers should stop using the product immediately and consult a healthcare provider for guidance.