cpsc regulated Recalls

2,142 recalls tagged with “cpsc regulated”.

Health & Personal Care
HIGH
FDA DRUG

Biocon Prazosin Hydrochloride 2 mg Capsules Recalled for Nitrosamine Impurity (58,896 bottles, 2026)

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‑

Prazosin Hydrochloride
cGMP deviation:
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Food & Beverages
HIGH
FDA FOOD

Zarlengo Italian Ice Recalls Chocolate Chocolate Chip Gelato Over Soy Lecithin Ingredient Mismatch (

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
Soy Lecithin
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Recalled Sunnyyes LED Lights with remote controls
HIGH
CPSC

Sunnyyes LED Mini Lights Recalled for Battery Ingestion Risk, Despite Reese’s Law Violations

Sunnyyes LED mini lights are recalled after reports of serious injury risk from accessible coin batteries. The recall covers Sunnyyes branded lights sold nationwide. The hazard stems from lithium coin batteries accessible to children, plus a loose remote-control battery screw and missing parental warnings. Stop using the product and contact Sunnyyes for a full refund.

Sunnyyes LED Mini Lights
The recalled
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Recalled Vive Health Compact Bed Rail (model number LVA2009SLV)
HIGH
CPSC

Vive Health Bed Rails Recall Expands as Entrapment, Asphyxiation Risk Causes Two Deaths

Vive Health recalled adult portable bed rails after two deaths were linked to entrapment and asphyxiation. The recall covers the Compact Bed Rail model LVA2009SLV, Bed Rail Collection V model LVA2097SLV, and LVA1024 units purchased on or before August 21, 2023. A prior recall covered LVA1024 units purchased after that date. Consumers must stop using these rails and seek a full refund from Vive.

Vive Health
When the
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Recalled 4our Kiddies Plastic Tip Restraint
HIGH
CPSC

4our Kiddies Tip Restraint Kits Recalled Over Tip-Over Hazard in 2026

Fourour Kiddies recalled tip restraint kits after tests found plastic components could break, creating a tip-over risk. The recall affects kits used to secure furniture to walls. Consumers should stop using the recalled restraints and seek a stainless steel replacement from 4our Kiddies.

4our Kiddies
The recalled
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Recalled AirClub Convertible Bassinet – Front View light grey
MEDIUM
CPSC

AirClub Recalling convertibles Bassinets for Bedside Sleepers Over Fall Hazard (2026)

AirClub recalled convertible bassinets that convert into bedside sleepers due to a hazardous attachment mechanism. The recall affects models labeled QX-831. The defect creates an opening between the bedside sleeper and mattress, posing a risk of serious injury or death to infants. Stop using the product immediately and contact AirClub for a replacement attachment mechanism.

AirClub
The recalled
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Health & Personal Care
HIGH
FDA DRUG

ARTIFICIAL TEARS Eye Drops Recalled for Sterility Concerns, 720 Bottles Distributed Nationwide (2026

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.

ARTIFICIAL TEARS
Lack of
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Food & Beverages
HIGH
FDA FOOD

Connecticut Crab Company Crab Cakes Recalled for Temperature Abuse Risk, 39 Boxes Affected

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.

Connecticut Crab Company
May be
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Health & Personal Care
HIGH
FDA DRUG

Fagron Compounding Services Vancomycin HCl 1 g in 250 mL NS Injection Recall Expands in 2026

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.

Fagron Compounding Services
Lack of
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Food & Beverages
HIGH
FDA FOOD

Riverence Smoked Trout Dip Recall for Milk Allergen Labeling Error (High)

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.

Riverence Provisions
Label declares
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Recalled Aisstxoer Adult Bike Helmet (pink)
HIGH
CPSC

Aisstxoer Adult Bicycle Helmets Recalled Over Head Injury Risk (2026)

Aisstxoer adult bicycle helmets sold on Amazon by YXTDZ Store are being recalled. The helmets fail to meet mandatory safety standards for impact attenuation and stability, creating a serious head-injury risk. Stop using the recalled helmet now and contact YXTDZ Store for a full refund; destroy the helmet and email a photo to yxtdzamz@126.com.

Aisstxoer Adult Bicycle Helmets
The recalled
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Tag Statistics

Total Recalls
2,142

Related Tags

chemical hazardpoisoning riskstop use immediatelyreturn for refundfda regulatednhtsa regulatedlithium batteryglassinfant productadult productimmediate actionbattery powered