Product Recalls in Alaska
Product recalls affecting Alaska — including food, drugs, consumer products, medical devices, and vehicles distributed to Alaska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,336 recalls have been distributed to Alaska in the last 12 months.
Showing 25941–25960 of 27,254 recalls
Recalled Item: DePuy Spine VIPER POLY SCREW 5.5 8 X70MM Tl Product Recalled by DePuy Spine,...
The Issue: Polyaxial screws 8x 80 and larger may disassociate when inserting in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Echo Bi-Metric Press-Fit Stems/Echo Bi-Metric 11mm x 135mm Collarless Porous...
The Issue: It was reported that the surgeon noticed that the Echo 11mm hip stem had an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix PMIC-108 Panels Recalled by Becton Dickinson & Co. Due to An...
The Issue: An antibiotic susceptibility test kit may produce false intermediate or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare Height Adjustable (walking) Canes Recalled by Invacare Corporation...
The Issue: Following their receipt of several customer complaints, Invacare recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ethicon Endo-Surgery Inc. The ENSEAL¿ G2 Tissue Sealers are indicated...
The Issue: Potential for self activation while the device is in use, which may result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OmniGuide BP-ROBOTIC ( BeamPath Robotic) Recalled by OmniGuide, Inc. Due to...
The Issue: Failure of glue joint, allowed a portion of the single use device to shift...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arobella Medical 6mm Qurette used with the Arobella Medical AR1000 Recalled...
The Issue: This recall has been initiated because the Arobella Medical 6mm Qurette Q07...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAYFIELD Composite Series Base Unit Recalled by Integra LifeSciences...
The Issue: An investigation of an adverse trend of complaints conducted by Integra...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lifestyles Pleasure Collection 30 Premium Lubricated Condoms Assortment of...
The Issue: One lot of Lifestyles Pleasure Collection Lubricated Condoms is misbranded....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laparoscope Recalled by Applied Medical Resources Corp Due to Applied...
The Issue: Applied Medical is conducting a voluntary recall on a specific lot number of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Access hLH assay is a paramagnetic particle Recalled by Beckman Coulter...
The Issue: Beckman Coulter Inc. (BEC) has demonstrated that real time stability testing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAYFIELD Composite Series Skull Clamps Recalled by Integra LifeSciences...
The Issue: An investigation of an adverse trend of complaints conducted by Integra...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDRAD Hand Controller Sheath Recalled by Medrad Inc Due to The seal between...
The Issue: The seal between the white polyethylene and the clear plastic may be missing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LAD SILI CONE SINGLE USE Recalled by King Systems Corp. Due to The firm...
The Issue: The firm received two complaints from a user facility in New Jersey...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Trauma Nail System. The devices are indication for bone fixation....
The Issue: Recall was initiated due to the possibility that the outer pouch was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LAD Standard ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...
The Issue: The firm received two complaints from a user facility in New Jersey...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LAD Standard ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...
The Issue: The firm received two complaints from a user facility in New Jersey...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LAD SILI CONE SINGLE USE Recalled by King Systems Corp. Due to The firm...
The Issue: The firm received two complaints from a user facility in New Jersey...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LAD SILI CONE SINGLE USE Recalled by King Systems Corp. Due to The firm...
The Issue: The firm received two complaints from a user facility in New Jersey...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LAD Standard ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...
The Issue: The firm received two complaints from a user facility in New Jersey...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.