Recalls
Recall: Joolz Aer2 Car Seat Adapters for Strollers
Joolz Recalls Aer2 Car Seat Adapters for Strollers Due to Risk of Serious Injury from Fall Hazard Name of Product: Joolz Aer2 Car Seat Adapters for Joolz Aer 2 Stroller Hazard: The recalled car seat adapters can fail to properly attach to the stroller, which may allow...
Recall: BABESIDE Doll and Stroller Children’s Toys
BABESIDE Doll and Stroller Children’s Toys Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violate Small Parts Ban; Sold on Amazon by HYBDOLLS Name of Product: BABESIDE Doll and Stroller Toys Hazard: The recalled toys violate the small parts...
Recall: CooCooBaby Baby Loungers
CooCooBaby Baby Loungers Recalled Due to Risk of Serious Injury or Death from Suffocation and Fall Hazards; Violates Mandatory Standard for Infant Sleep Products Name of Product: CooCooBaby Baby Loungers Hazard: The baby loungers violate the mandatory standard...
Recall: GOPO Toys
GOPO Toys Recalls Pull String Teething Toys Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys Name of Product: GOPO TOYS Pull String Teething Toys Hazard: The recalled teething toys violate the mandatory standard...
Recall: Montessori Busy Board Toys
Montessori Busy Board Toys Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys; Sold on Amazon by Small Fish Name of Product: Small Fish Montessori Busy Board Toys Hazard: The busy boards violate...
Recall: Raychy Children’s Light Sneakers
Raychy Children's Light Sneakers Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Coin Batteries; Imported by Carina and Rambo Name of Product: Raychy Children's Light Sneakers Unisex Hazard:...
Embolization Device Recall and Correction
Embolization Device Recall and Correction: Medtronic Removes Unused 027 Compatible Pipeline Vantage Embolization Device with Shield Technology, Updates Use Instructions for 021 Compatible Pipeline Vantage Embolization Devices due to Increased Risk of Incomplete Wall...
Power Assist Device Recall
Power Assist Device Recall: Max Mobility/Permobil Removes SpeedControl Dial Component Used with SmartDrive MX2+ Power Assist Device Due to Risk for Motor to Be Unresponsive to the User Max Mobility/Permobil is recalling the SpeedControl Dial component used with the...
Potential to Miss Critical Safety Alerts for Smartphone-Compatible Diabetes Devices
The U.S. Food and Drug Administration (FDA) is alerting patients who use diabetes devices, as well as their caregivers and health care providers, of a safety concern regarding diabetes devices, such as continuous glucose monitors (CGMs), insulin pumps and automated...
Continuous Ventilator Correction
Continuous Ventilator Correction: Baxter Healthcare Corporation Issues Correction for Life2000 Ventilator due to a nonconforming battery charger, which triggers a battery alarm and renders the ventilator inoperable Baxter Healthcare Corporation is correcting the...
Oxygen Concentrator Recall
Oxygen Concentrator Recall: JIANGSU JUMAO X-CARE MEDICAL EQUIPMENT CO LTD Removes JMC5A Ni/TruAire-5 Oxygen Concentrator due to the devices spontaneously catching fire JIANGSU JUMAO X-CARE MEDICAL EQUIPMENT CO LTD is recalling devices due to incidents of device...
Infusion Pump Battery Recall
Infusion Pump Battery Recall: ICU Medical Removes Some CSB Batteries Intended For Use With Plum 360, A+, and A+3 Infusion Systems Due to Reports of Allegedly Counterfeit, Untested Batteries In Use ICU Medical is recalling some CSB batteries that are intended for use...