cpsc regulated Recalls

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

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

CCCEI Brand Power Strips Recalled for Fire Risk Sold by Middle Way Electronics (2026)

CCCEI Brand power strips are recalled after a potential fire risk due to missing overcurrent protection. The recall covers 6ft, 10ft, and 15ft models sold by Middle Way Electronics. Consumers should stop using the product and request a full refund.

MPINOI Adult Portable Bed Rails Recalled for Entrapment and Asphyxiation Risk

This recall involves MPINOI-branded adult portable bed rails. The white metal bed rails measure about 15 inches wide by 26 inches tall and have an extendable handle with gray padding and a black storage mesh pocket. "MPINOI" is printed on the mesh pocket.

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

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

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

Lack of Assurance of Sterility

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

May be temperature abused, which may result in growth of Clostridium botulinum

Omnipaque Injection Recalled by GE Healthcare for Particulate Matter in 866,570 vials (2026)

GE Healthcare Omnipaque Iohexol Injection Recall Expanded for Particulate Matter in 306,810 Vials (D

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

Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port

Fagron Compounding Services Norepinephrine Bitartrate Injection Recall Affects 5,140 Bags (2026)

Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port

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

Clonidine Transdermal System Recall Expanded for CGMP Deviations in 113,943 Cartons (2026)

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.

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

Label declares cream cheese but does not declare milk

Teva Clonidine Transdermal System Recall Expands Over CGMP Deviations, 124,054 Cartons Affected (202

CGMP Deviations: use of an unapproved raw material

Goregent Infant Walkers Recalled for Fall Hazard on Amazon (2026)

Specialized Recalls 2026 Turbo Como SL Electric Bicycles Over Fork Fatigue Crack Fall Hazard

Teva Octreotide Acetate Injectable Suspension Recall 21,930 Cartons Over Sterility Risk (2026)

Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.

Curosurf 240 mg Poractant Alfa Recalled for Sterility Concerns (2026)

Chiesi USA recalled 7,235 Curosurf vials distributed nationwide to hospitals and clinics. The recall cites a lack of assurance of sterility. Healthcare providers should stop using the product immediately and contact Chiesi USA for guidance.