United States Recalls
Consumer recalls from the FDA, CPSC, NHTSA, and USDA FSIS.
Khong Guan Corporation Issues Recall of Glutinous Rice Balls With Black Sesame Filling Due to Undeclared Peanuts
WonderStone Infant Walkers Recalled Due to Risk of Serious Injury or Death from ...
The recalled infant walkers violate the mandatory standard for infant walkers because they can fit through a standard doorway and fail to stop at the edge of a step, posing a risk of serious injury or death due to a fall hazard.
Best Buy Recalls Insignia® Gas Ranges Due to Risk of Serious Injury from a Fire ...
The recalled ranges' front-mounted knobs can be activated accidentally by humans or pets, posing a risk of serious injury from a fire hazard.
Greenworks Tools Recalls 24V and 48V Kobalt Yard Power Tools with USB-C Batterie...
Charging the lithium-ion batteries through the USB-C port, while the batteries are inserted in the yard power tools can cause the batteries to short-circuit, posing a risk of serious injury from fire hazard.
Biometric Gun Safes Recalled Due to Serious Injury Hazard and Risk of Death; Sol...
The biometric lock on the gun safes can be opened by unauthorized users, posing a serious injury hazard and risk of death.
Moodooy Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapmen...
The recalled bed rails violate the mandatory standard for?adult portable bed rails?because users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation.?In addition, the bed rails do not bear the required hazard warning labels.
Conair Recalls Cuisinart Propel+ Four Burner 3-In-1 Gas Grills Due to Risk of Se...
The tempered glass window in the pizza oven can shatter during use, posing a risk of serious injury from laceration hazard.
Flaunt Recalls Magsafe Battery Chargers Due to Risk of Serious Injury or Death f...
The lithium-ion battery in the recalled power banks (chargers) can overheat and ignite, posing a risk of serious injury or death from fire and burn hazards.
Medline Convenience kits containing recalled Swan-Ganz Catheters CV ANESTHESI...
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication loss, and/or blood loss.
CRE Wireguided 6-8mm 240cm
Potential sterile breach of the pouches in which devices are packaged.
CRE Wireguided 18-20mm 240cm
Potential sterile breach of the pouches in which devices are packaged.
CK000980A PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741236150 ...
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Depuy Synthes, ATTUNE Revision Hinge Knee Hinge Housing Components with the belo...
The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
Medline Convenience kits containing recalled Swan-Ganz Catheters RIGHT HEART ...
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication loss, and/or blood loss.
Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator...
In certain cases, a collimator may not fully dock, which triggers a system interlock and prevents motion from the operator console. If personnel then enter the treatment room and initiate motion using the in-room control pendant, the collimator may release and fall from the housing.
OTP5000 THORA/PARA TRAY, 5FR, NON-VALVED UDI-DI Code: 0110885403284748 PIG12...
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Brand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Sy...
Potential sterility breach in sealing area of sterile pouch. If used, issue may result in moderate localized infection. If discovered prior to use, may result in clinically insignificant extension of surgery to find another readily available device.
A M S, ALIGNED MEDICAL SOLUTIONS, Thyroid FNA Pack-RX, Pack Number AMS17729, sur...
Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.
CRE Wireguided 12-15mm 240cm
Potential sterile breach of the pouches in which devices are packaged.
A M S, ALIGNED MEDICAL SOLUTIONS, Dr. Lewin Pack, Pack Number AMS7200D, surgical...
Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.
ARTIS icono floor. Model Number: 11327700.
Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits.
Depuy Synthes, ATTUNE Revision Hinge Knee Hinge Insert Components with the below...
The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.
7617408 Groshong NXT ClearVue Catheter 4 Fr Single-Lumen UDI-DI Code: 008017410...
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
CRE Wireguided 15-18mm 240cm
Potential sterile breach of the pouches in which devices are packaged.