Vereinigte Staaten Recalls
Verbraucherrückrufe von FDA, CPSC, NHTSA und USDA FSIS.
NHTSAJayco, Inc. - Auto Level Jacks may be Lowered during Transit
Jayco, Inc. - Auto Level Jacks may be Lowered during Transit
Activation of the jacks during transit increases the risk of a crash.
CPSCPlay Yard and Crib Mattresses Recalled Due to Risk of Serious Injury or Death from Entrapment and Fire Hazards; Violate Mandatory Standards for Mattresses; Sold on Amazon by Voomf
Play Yard and Crib Mattresses Recalled Due to Risk of Serious Injury or Death from Entrapment and Fire Hazards; Violate Mandatory Standards for Mattresses; Sold on Amazon by Voomf
The recalled mattresses violate the mandatory safety standard for crib mattresses because the mattresses may not adequately fit certain play yards, posing a deadly entrapment hazard. Babies can suffocate in gaps between an undersized mattress, or extra padding, and side walls of a product, especially when the infant's face becomes trapped against the side and the mattress, preventing the infant from breathing. Furthermore, the full-sized crib mattresses violate the mandatory flammability standard for mattress sets, posing a risk of serious injury or death from fire.
NHTSAChrysler (FCA US, LLC) - Seat Belt May Twist and Fail to Retract Properly
Chrysler (FCA US, LLC) - Seat Belt May Twist and Fail to Retract Properly
A seat belt that does not retract properly may fail to restrain an occupant as intended, increasing the risk of injury.
NHTSAInternational Motors, LLC - Windshield Wipers May Disconnect from Motor
International Motors, LLC - Windshield Wipers May Disconnect from Motor
Inoperative windshield wipers can reduce the driver's visibility, increasing the risk of a crash.
CPSCWinston Porter and Seeday 3-Drawer, 4-Drawer, and 5-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units
Winston Porter and Seeday 3-Drawer, 4-Drawer, and 5-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units
The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or death to children. The dressers violate the mandatory safety standard as required by the STURDY Act.
CPSCWnttmt Baby Walkers Recalled Due to Risk of Serious Injury or Death from Fall and Entrapment Hazards; Violate Mandatory Standard for Infant Walkers; Sold on Amazon by WURUI.BABY
Wnttmt Baby Walkers Recalled Due to Risk of Serious Injury or Death from Fall and Entrapment Hazards; Violate Mandatory Standard for Infant Walkers; Sold on Amazon by WURUI.BABY
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 deadly fall hazard. In addition, the infant walkers have leg openings that allow the child to slip down until the child's head can become entrapped, posing a risk of serious injury or death.
CPSCHead Watersports Recalls Apeks Second Stage Scuba Regulators Recalled Due to Risk of Serious Injury or Death from Drowning Hazard
Head Watersports Recalls Apeks Second Stage Scuba Regulators Recalled Due to Risk of Serious Injury or Death from Drowning Hazard
The recalled second stage regulators can restrict air flow to the user at depths exceeding 45 meters (approximately 147 feet), posing risk of serious injury or death from a drowning hazard.
CPSCLouisville Ladder Recalls Over One Million Attic Stairway Ladders Due to Risk of Serious Injury or Death from Fall Hazard
Louisville Ladder Recalls Over One Million Attic Stairway Ladders Due to Risk of Serious Injury or Death from Fall Hazard
The bolts on the attic stairway ladders can break while in use, posing a risk of serious injury or death from fall hazard.
CPSCMagnetic Fidget Sliders Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys; Sold on Amazon by PIXLABBY
Magnetic Fidget Sliders Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys; Sold on Amazon by PIXLABBY
The magnetic fidget sliders violate the mandatory standard for toys because they can liberate loose high-powered magnets posing an ingestion hazard to children. When high-powered magnets are swallowed, the ingested magnets can attract each other or other metal objects and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.
CPSCA2batt Recalls EEMB Lithium Coin Battery Chargers Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Coin Batteries
A2batt Recalls EEMB Lithium Coin Battery Chargers Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Consumer Products with Coin Batteries
The recalled battery chargers violate the mandatory standard for consumer products containing button cell or coin batteries, because the charger has lithium coin batteries that can be accessed easily by children. In addition, the coin batteries provided with the battery charger are not in child-resistant packaging, and the packaging does not have the warnings, as required by Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.
NHTSAVolvo Trucks North America - Marker Lights May Fail to Illuminate/FMVSS 108
Volvo Trucks North America - Marker Lights May Fail to Illuminate/FMVSS 108
Marker lights that fail to illuminate can reduce visibility, increasing the risk of a crash.
NHTSARivian Automotive, LLC - Front Exterior Turn Signals May Fail/FMVSS 108
Rivian Automotive, LLC - Front Exterior Turn Signals May Fail/FMVSS 108
Turn signals that do not function properly increase the risk of a crash.
NHTSAToyota Motor Engineering & Manufacturing - Deactivated Electronic Stability Control/FMVSS 126
Toyota Motor Engineering & Manufacturing - Deactivated Electronic Stability Control/FMVSS 126
Driving with a disabled electronic stability control system or continuously illuminated brake lights can increase the risk of a crash.
NHTSAEvenflo Company, Inc. - Incorrect Indicator for Recline Position/FMVSS 213
Evenflo Company, Inc. - Incorrect Indicator for Recline Position/FMVSS 213
A child seat that is not reclined as intended increases the risk of injury in a crash.
CPSCWichard Groupe North America Recalls Courant Spliced Kalimba Climbing Ropes Due to Risk of Serious Injury or Death from Fall Hazard
Wichard Groupe North America Recalls Courant Spliced Kalimba Climbing Ropes Due to Risk of Serious Injury or Death from Fall Hazard
The spliced termination ends on the recalled ropes can fail unexpectedly, posing a risk of serious injury or death from fall hazard.
NHTSAChrysler (FCA US, LLC) - Seat Belt May Twist and Fail to Retract Properly
Chrysler (FCA US, LLC) - Seat Belt May Twist and Fail to Retract Properly
A seat belt that does not retract may fail to restrain properly an occupant as intended, increasing the risk of injury.
FDA DevicesEOPA Elongated One-Piece Arterial Cannula BLUNT 22FR, intended for use with cardiopulmonary bypass as an arterial return cannula, Model Number 77522
EOPA Elongated One-Piece Arterial Cannula BLUNT 22FR, intended for use with cardiopulmonary bypass as an arterial return cannula, Model Number 77522
Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforation, hypotension, ischemia, and organ dysfunction.
FDA DevicesL-Cath PICC S/L Peripherally Inserted Central Catheter: 26ga (1.9F) 0.60mm x 30cm, REF: 384539; 18ga (3.5F) 1.15mm x 60cm, REF: 384464; Basic Kit 28GA (1.2F) x 25cm 1 Lumen), REF: 384516; 20ga (3F) 1.00mm x 60cm, REF: 384463
L-Cath PICC S/L Peripherally Inserted Central Catheter: 26ga (1.9F) 0.60mm x 30cm, REF: 384539; 18ga (3.5F) 1.15mm x 60cm, REF: 384464; Basic Kit 28GA (1.2F) x 25cm 1 Lumen), REF: 384516; 20ga (3F) 1.00mm x 60cm, REF: 384463
Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients; and sampling, may experience leaking and/or cracking at the hub, which may lead to replacement, inability to flush/aspirate catheter, catheter occlusion, therapy interruption, blood loss, tissue irritation, bloodstream infection.
FDA DevicesGEM Premier 5000 with IQM2 Model/Catalog Number: 00024019255 and GEM Premier 7000 with iQM3 Model/Catalog Number: 00000015279 Portable blood analyzer system. Affected Accessory: Bar Code Reader (BCR) Wand Part No. 00024015859
GEM Premier 5000 with IQM2 Model/Catalog Number: 00024019255 and GEM Premier 7000 with iQM3 Model/Catalog Number: 00000015279 Portable blood analyzer system. Affected Accessory: Bar Code Reader (BCR) Wand Part No. 00024015859
Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID.
FDA DevicesResmed Astral 100/150 Resmed Astral 100/50 is a ventilator system that provides continuous or intermittent ventilatory support for patients weighing more than 11lb (5kg) who require mechanical ventilation.
Resmed Astral 100/150 Resmed Astral 100/50 is a ventilator system that provides continuous or intermittent ventilatory support for patients weighing more than 11lb (5kg) who require mechanical ventilation.
Due to a Supercapacitor electrolyte leakage on Printed Circuit Board Assembly (PCBA) may damage the charger chip, causing fail-safe state and interruption of ventilation therapy.
FDA FoodDQ Chocolate Reduced Fat Ice Cream Mix, 5 GAL (18.9L). Keep refrigerated.
DQ Chocolate Reduced Fat Ice Cream Mix, 5 GAL (18.9L). Keep refrigerated.
Foreign material found in product (identified as metal shavings)
FDA FoodRequeson (soft ricotta) 1 lb. packed into a clear clamshell package with no labeling information. "Requeson" is handwritten in black marker on the top lid of the clamshell package. No lot code or UPC.
Requeson (soft ricotta) 1 lb. packed into a clear clamshell package with no labeling information. "Requeson" is handwritten in black marker on the top lid of the clamshell package. No lot code or UPC.
Products may be contaminated with Listeria monocytogenes.
FDA DevicesAMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) ENT Pack, Pack Number AMS12206; 2) ENT Pack, Pack Number AMS15517; 3) ENT Facial Pack, Pack Number AMS15863A.
AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) ENT Pack, Pack Number AMS12206; 2) ENT Pack, Pack Number AMS15517; 3) ENT Facial Pack, Pack Number AMS15863A.
The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998C due to potential for unexpected variability of endotoxin levels on the products.
FDA DevicesOsteoBallast, 45 x 17.5 mm (SeaSpine Brand), REF: 56800095. Ballast, 45 x 17.5 mm (IsoTis Brand), REF: 02-8000-095
OsteoBallast, 45 x 17.5 mm (SeaSpine Brand), REF: 56800095. Ballast, 45 x 17.5 mm (IsoTis Brand), REF: 02-8000-095
Demineralized bone matrix (DBM) in resorbable mesh indicated for use with autograft as a bone graft extender in the posterolateral spine and pelvis, were filled with approx. 4.5 cc DBM (fill for 45 ¿ 11 mm configuration) instead of approx. 7.5 cc DBM (fill for 45 ¿ 17.5 mm configuration), which may lead to delayed fusion, incomplete fusion, pseudarthrosis, or lack of bone ingrowth.