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. 2,361 recalls have been distributed to Alaska in the last 12 months.
Showing 21901–21920 of 27,254 recalls
Recalled Item: Philips Healthcare Xper vascular systems R7.6 Model : 722134 Product...
The Issue: Monitor Ceiling Suspension system may fall
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare INTEGRIS H5000F/Allura 9F Model : 722017 Product Usage:...
The Issue: Monitor Ceiling Suspension system may fall
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Inserter for Titanium Elastic Nails Recalled by Synthes, Inc. Due to...
The Issue: The Inserter has the potential for mechanical failures such as breakage of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Allura Xper Series: Allura Xper FD10 Allura Xper Recalled...
The Issue: Monitor Ceiling Suspension system may fall
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Allure BiPlane Series: Model 722013 Allura Xper FD20...
The Issue: Monitor Ceiling Suspension system may fall
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Xper vascular system Model : 722124 Product Usage:...
The Issue: Monitor Ceiling Suspension system may fall
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Manual Toothbrush Recalled by Norwex Usa Inc Due to The toothbrush head can...
The Issue: The toothbrush head can potentially disengage from the handle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Axial Torque Limiting Driver (1st generation) Product Usage: The Bradshaw...
The Issue: A component failure could cause a situation where the applied torque was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD" Medication Cassette Reservoir Recalled by Smiths Medical ASD, Inc. Due...
The Issue: Smiths Medical has become aware of an issue with specific lots of 50mL CADD"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare¿ Pronto¿ Air Personal Transporter (power wheelchair) Recalled by...
The Issue: The batteries used in the Invacare¿ Pronto¿ Air Personal Transporter models...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Proteus XR/a with wall stand model number 2260354. Recalled by...
The Issue: Potential breakage of the steel cable which supports the bucky device in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Maquet...
The Issue: Power supply malfunction complaints related to suboptimal thermal management.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penner Patient Stretcher/Transfer Lift System Models 391000-1 and 392000-1...
The Issue: If the patient sits on either wing, not squarely on the center section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard 100% Latex-Free Urinary Drainage Bag with Anti- Chamber and Recalled by...
The Issue: Potential breach of the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta Precise Treatment Table Recalled by Elekta, Inc. Due to It is...
The Issue: It is possible to position the Treatment Table with errors greater than 5mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Trabecular Metal Tibial Plate / Persona TM Tibia-Prosthesis Recalled...
The Issue: An increase in complaints of loosening and radiolucent lines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9F Plastic Dual Port Recalled by Medical Components, Inc dba MedComp Due to...
The Issue: The dual port with catheters was not covered under FDA clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Systems Progesterone Kit Recalled by Siemens Healthcare...
The Issue: ADVIA Centaur Systems Progesterone Kit Lots Ending in 268 have a high bias...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Systems Progesterone Kit Recalled by Siemens Healthcare...
The Issue: ADVIA Centaur Systems Progesterone Kit Lots Ending in 268 have a high bias...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Engstrom Carestation Recalled by GE Healthcare Due to...
The Issue: Potential failure of the caster mounting hardware, which may result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.