Vereinigte Staaten Recalls
Verbraucherrückrufe von FDA, CPSC, NHTSA und USDA FSIS.
NHTSAVolvo Car USA, LLC - Seat Belt Warning System Malfunction/FMVSS 208
Volvo Car USA, LLC - Seat Belt Warning System Malfunction/FMVSS 208
An audible warning chime that does not properly alert of an unbelted seat belt can increase the risk of injury during a crash.
FDA DevicesEsaote Endocavity ultrasonic probe, Model E 3-12, REF 120000038
Esaote Endocavity ultrasonic probe, Model E 3-12, REF 120000038
A potential weakness has been identified in the probe body, so that, in a specific production batch, liquid may leak from the terminal part of the casing near the cable.
NHTSAMercedes-Benz USA, LLC - Incorrectly Installed Cable May Prevent Door from Opening
Mercedes-Benz USA, LLC - Incorrectly Installed Cable May Prevent Door from Opening
A door that cannot be opened may trap occupants inside the vehicle, which can increase the risk of injury.
NHTSAPebble Mobility Inc. - Solar Panel May Detach
Pebble Mobility Inc. - Solar Panel May Detach
A detached solar panel can become a road hazard for other vehicles, increasing the risk of a crash.
NHTSAKia America, Inc. - Rear Seat Belt Buckle May Not Latch
Kia America, Inc. - Rear Seat Belt Buckle May Not Latch
A seat belt buckle that is not latched properly can fail to restrain an occupant in a crash, increasing the risk of injury.
CPSCCubimana Island Storm 3 In 1 Building Sets Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys; Sold on Amazon by RBS Toys
Cubimana Island Storm 3 In 1 Building Sets Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys; Sold on Amazon by RBS Toys
The Island Storm Building Sets violate the mandatory safety standard for toys because the battery compartment within the LED light piece contains button cell batteries that can be easily accessed by children. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.
CPSCHALO Dream Recalls Magic Sleepsuits Due to Choking Hazard
HALO Dream Recalls Magic Sleepsuits Due to Choking Hazard
The zipper head can detach from certain sleepsuits, posing a choking hazard to infants.
CPSCUnique Brands Com Recalls Forever 21 Pajama Pants Due to Risk of Serious Injury or Death from Burn Hazard; Violates Mandatory Flammability Standards for Children's Sleepwear
Unique Brands Com Recalls Forever 21 Pajama Pants Due to Risk of Serious Injury or Death from Burn Hazard; Violates Mandatory Flammability Standards for Children's Sleepwear
The recalled children's pajama pants violate the mandatory standards for flammability of children's sleepwear, posing a burn hazard and risk of serious injury or death to children.
NHTSAToyota Motor Engineering & Manufacturing - Second-Row Seat Backs May Fail to Lock
Toyota Motor Engineering & Manufacturing - Second-Row Seat Backs May Fail to Lock
A seat back that fails to lock may not properly restrain an occupant during a crash, increasing the risk of injury.
NHTSAMitsubishi Fuso Truck of America, Inc. - Software Error may Prevent Vehicle from being Driven
Mitsubishi Fuso Truck of America, Inc. - Software Error may Prevent Vehicle from being Driven
A vehicle that is unable to move as needed, increasing the risk of a crash.
NHTSAWebasto Thermo & Comfort NA, INC - High Voltage Battery May Fail and Cause Fire
Webasto Thermo & Comfort NA, INC - High Voltage Battery May Fail and Cause Fire
Battery failure can cause a loss of drive power, increasing the risk of a crash. Battery failure can also increase the risk of a fire.
CPSCTomum Minoxidil Hair Serum Spray Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging; Distributed by Belleka
Tomum Minoxidil Hair Serum Spray Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging; Distributed by Belleka
The hair serum contains minoxidil, which must be in child-resistant packaging as required by the Poison Prevention Packaging Act. The hair serum's bottles are not child-resistant, posing a risk of serious injury or death from poisoning if the contents are swallowed by young children.
NHTSAESCAPE TRAILER INDUSTRIES LTD. - Spare Tire Carrier May Detach
ESCAPE TRAILER INDUSTRIES LTD. - Spare Tire Carrier May Detach
A detached carrier can become a road hazard for other vehicles, increasing the risk of a crash or injury.
NHTSAGeneral Motors, LLC - Engine Stall Due to Disabled Rear Fuel Pump
General Motors, LLC - Engine Stall Due to Disabled Rear Fuel Pump
An engine stall increases the risk of a crash.
NHTSAForest River, Inc. - Electrical Distribution Panel Not Properly Grounded
Forest River, Inc. - Electrical Distribution Panel Not Properly Grounded
An energized chassis increases the risk of injury and electrocution.
NHTSAGeneral Motors, LLC - Tire Sidewall Damage
General Motors, LLC - Tire Sidewall Damage
A tire with sidewall damage may experience sudden air loss or driver loss of control, increasing the risk of a crash.
NHTSAForest River, Inc. - Improperly Stripped Wires May Cause Electrical Arcing
Forest River, Inc. - Improperly Stripped Wires May Cause Electrical Arcing
Exposed conductors may cause electrical arcing, increasing the risk of a fire.
FDA DevicesMedline Convenience Kits: 1) NAIL KIT, Model Number: DYKM1528
Medline Convenience Kits: 1) NAIL KIT, Model Number: DYKM1528
Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required sterility assurance level required for sterile products.
FDA FoodFish Ball, Frozen, 20 pieces per pack, 400g Wt. UPC# 810093891325
Fish Ball, Frozen, 20 pieces per pack, 400g Wt. UPC# 810093891325
Undeclared allergen ingredient (Wheat and Sesame)
FDA DevicesOlympus Cystoscope Outer Sheath; Model/Catalog number: WA22810A;
Olympus Cystoscope Outer Sheath; Model/Catalog number: WA22810A;
Product being removed due to incompatibility when used in conjunction with a GreenLight Laser for BPH therapy which could damage the tip of the device.
FDA DrugsAmantadine HCl, Capsules, UPS, 100 mg, 50 Capsules (5 x 10) unit dose, Rx Only, Manufactured for: AvKARE, Pulaski, TN 38478, www.avkare.com, NDC 50268-069-15.
Amantadine HCl, Capsules, UPS, 100 mg, 50 Capsules (5 x 10) unit dose, Rx Only, Manufactured for: AvKARE, Pulaski, TN 38478, www.avkare.com, NDC 50268-069-15.
Failed Dissolution Specifications: This recall has been initiated due to an Out of Specification finding in dissolution.
FDA DevicesMedline Kits containing Tego Connectors: Medline IR Pack, SKU DYNJ67205C Medline NO CATHETER DIALYSIS INSERTION, SKU CVI5200
Medline Kits containing Tego Connectors: Medline IR Pack, SKU DYNJ67205C Medline NO CATHETER DIALYSIS INSERTION, SKU CVI5200
Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing. These issues may result in an occluded fluid path identified by the inability of the user to inject or withdraw blood product with a syringe. Damaged seals may also result in delay in therapy or fluid leakage, interruption in therapy, exposure to biological contaminants or air infused into the body.
FDA DevicesCampy CVA Medium 100/PK, R01272
Campy CVA Medium 100/PK, R01272
Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.
FDA DrugsAdbry, (tralokinumab-ldrm) injection, 300 mg/2mL, Packaged as a) 1 x Single dose Autoinjector, SAMPLE NOT FOR SALE, NDC 50222-350-91; b) 2 x Single dose Autoinjectors, NDC 50222-350-02; Rx only, Manufactured by: LEO Pharma A/S. Industriparken 55, DK-2750 Ballerup, Denmark, Distributed by: LEO Pharma Inc., Madison, NJ 07940, USA,
Adbry, (tralokinumab-ldrm) injection, 300 mg/2mL, Packaged as a) 1 x Single dose Autoinjector, SAMPLE NOT FOR SALE, NDC 50222-350-91; b) 2 x Single dose Autoinjectors, NDC 50222-350-02; Rx only, Manufactured by: LEO Pharma A/S. Industriparken 55, DK-2750 Ballerup, Denmark, Distributed by: LEO Pharma Inc., Madison, NJ 07940, USA,
Lack of Assurance of Sterility: due to the presence of particulate matter in one unit from the lot, which lab tests have identified as wool fiber.