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 15121–15140 of 27,254 recalls
Recalled Item: CombiDiagnost R90 (Stitching Patient Support) 709030 Recalled by Philips...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4.1 High Performance (Stitching Patient Support) 712031...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost Classic Recalled by Philips Medical Systems Gmbh, DMC Due to...
The Issue: The hook does not securely hold the footplate in the vertical position....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genicon EZee Single Use Specimen Retrieval Bag - Product Usage: Recalled by...
The Issue: Genicon is providing updated IFU labeling to users to provide clarity on how...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monitor with one Blood Parameter Module and one HSat Probe Recalled by...
The Issue: H/Sat Hybrid Intensity Shift has been seen in a subset of the H/Sat...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood parameter monitoring system 500 H/SAT Recalled by Terumo...
The Issue: H/Sat Hybrid Intensity Shift has been seen in a subset of the H/Sat...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERPORT CLEARVUE isp Recalled by Bard Peripheral Vascular Inc Due to...
The Issue: Certain NAUTILUS DELTA Port Kit product code / lot number combinations may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: This is an accessory to Intelect Advanced Recalled by DJO, LLC Due to The...
The Issue: The device accessories were not labeled with appropriate latex warning.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Partial Knee System Spacer Block Alignment Tower Recalled by Zimmer...
The Issue: The PPK System Spacer Block Alignment Tower mating feature that mates with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aplicare Povidone Iodine Prep Pads packaged within Portex Pro-Vent Arterial...
The Issue: The povidone iodine prep pads packaged with the arterial blood sampling kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clarity Urocheck 10SG Urinalysis Strips Recalled by Clarity Diagnostics Llc...
The Issue: Clarity Diagnostics LLC discovered specific lots of Clarity 10SG Strips are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q. angiography system. Model 10848280 Recalled by Siemens Medical...
The Issue: Potential hardware issue which may cause thermal effects and possible damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aplicare Povidone Iodine Prep Pads packaged within Portex Pulsator Arterial...
The Issue: The povidone iodine prep pads packaged with the arterial blood sampling kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS Pheno Model 10849000. Interventional Fluoroscopic X-Ray System Product...
The Issue: Potential hardware issue which may cause thermal effects and possible damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percepta Quad CRT-P MRI SureScan Recalled by Medtronic Inc., Cardiac Rhythm...
The Issue: Potential for a device reset to occur in Percepta CRT-P MRI SureScan and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ossur Skull Pin Recalled by Ossur Americas Due to Halo system products...
The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ossur Recalled by Ossur Americas Due to Halo system products labeled MR...
The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ossur CB Resolve Recalled by Ossur Americas Due to Halo system products...
The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ossur OB Resolve Recalled by Ossur Americas Due to Halo system products...
The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ossur Skull Pin Recalled by Ossur Americas Due to Halo system products...
The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.