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. 2,353 recalls have been distributed to Alaska in the last 12 months.
Showing 24201–24220 of 46,762 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 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: DigitalDiagnost Dual Detector (Stitching Patient Support) 712022 Recalled by...
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 Flex / Value (Stitching Patient Support) 712028 Recalled...
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 Rel.4 Upgrades (Stitching Patient Support) 712084 Recalled...
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: Proteus 235 Recalled by Ion Beam Applications S.A. Due to Gantry rotation or...
The Issue: Gantry rotation or proton irradiation can be allowed even if apertures or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blissful Remedies Red Maeng Da Recalled by World Organix, LLC Due to...
The Issue: Microbial Contamination of Non-Sterile Products: The firm is initiating a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Blissful Remedies Red Maeng Da Liquid Kratom Mitragyna Speciosa Recalled by...
The Issue: Microbial Contamination of Non-Sterile Products: The firm is initiating a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Blissful Remedies Recalled by World Organix, LLC Due to Microbial...
The Issue: Microbial Contamination of Non-Sterile Products: The firm is initiating a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Blissful Remedies Kratom+CBD CBD infused Maeng Da Recalled by World Organix,...
The Issue: Microbial Contamination of Non-Sterile Products: The firm is initiating a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Blissful Remedies Gold Series Ultra Enhanced Indo Recalled by World Organix,...
The Issue: Microbial Contamination of Non-Sterile Products: The firm is initiating a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Enalapril Maleate Tablets Recalled by MAJOR PHARMACEUTICALS Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Sub-recall because this...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Enalapril Maleate Tablets Recalled by MAJOR PHARMACEUTICALS Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Sub-recall because this...
Recommended Action: Stop taking this medication. Contact your pharmacy or 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: 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: 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: 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: Acetylcysteine for Injection 6 g/30 mL (200 mg/mL). Rx Only. Recalled by...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or 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.