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. 2,440 recalls have been distributed to Alaska in the last 12 months.
Showing 15661–15680 of 27,254 recalls
Recalled Item: Allura Xper R8.x.25.5 and UNIZ systems (only with a FlexVision Recalled by...
The Issue: After continuous operation for more than one and a half days, the image on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray BCID Panel (Blood Culture Identification Panel) Recalled by...
The Issue: There is an increased risk of false positive Proteus results when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart FRx AED. Recalled by Philips Electronics North America...
The Issue: An issue with one of the electric components (a resistor) could result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHILIPS Xper Flex Cardio Physiomonitoring System Recalled by Invivo...
The Issue: The real-time numeric value for ventricular end-diastolic pressure (EDP)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImplantDirect simply InterActive Implant Recalled by Implant Direct Sybron...
The Issue: The cap on the vial might be labeled with the incorrect part number but the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesis Surgical Cassette Tapered Implants are intended for placement...
The Issue: The surgical cassette contained extra-large white grommets making the 3.8 mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Prestige LP(TM) Cervical Disc System with Streamlined Instruments...
The Issue: The firm received complaints of drill bits breaking during use with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power-LOAD Cot Fastening System Recalled by Stryker Medical Division of...
The Issue: The power load floor plates which hold the ambulance cot anchors in place...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vacuum Regulator Recalled by Ohio Medical Corporation Due to Final quality...
The Issue: Final quality control testing was not completed before the devices were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phoenix Nail System Recalled by Zimmer Biomet, Inc. Due to Certain lots of...
The Issue: Certain lots of the Phoenix Tibia Nail 3.5mm Inserter instruments are being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hinge Coupling Hoffmann LRF Catalog # 4933-0-800 Intended for fixation...
The Issue: The wrong parts were picked for packaging. The connecting Nuts were packed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5 mm Apple-Hunt Secondary Cannula/Pyramidal Tip Trocar - extended length...
The Issue: Products have been packaged with the wrong Trocar length type.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evicel Accessory Device - 45 cm Flexible Tip (SET OF 3) Recalled by Ethicon,...
The Issue: Products labeled for distribution outside the United States may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci X Surgical System Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Specific da Vinci X Surgical Systems (IS4200) were shipped with defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST-AIA PACK TU Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...
The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST-AIA PACK Testosterone Recalled by Tosoh Bioscience Inc Due to Asfotase...
The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST-AIA PACK Cort Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...
The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST-AIA PACK Prolactin Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...
The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST-AIA PACK FSH Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...
The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST-AIA PACK CA 19-9 Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...
The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.