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. 2,000 recalls have been distributed to Alaska in the last 12 months.
Showing 1641–1660 of 46,762 recalls
Recalled Item: Vial Label: Epinephrine Injection Recalled by PFIZER INC Due to Lack of...
The Issue: Lack of Assurance of Sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vial Label: 8.4% Sodium Bicarbonate Injection Recalled by PFIZER INC Due to...
The Issue: Lack of Assurance of Sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Halyard Recalled by AVID Medical, Inc. Due to Potential for open header bag...
The Issue: Potential for open header bag seals, compromising sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Recalled by AVID Medical, Inc. Due to Potential for open header bag...
The Issue: Potential for open header bag seals, compromising sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PhD Hemostasis Valve Recalled by Merit Medical Systems, Inc. Due to...
The Issue: Hemostasis valve has a manufacturing defect and when used the valve cap may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion System configured with a 1 Phase UPS. Azurion family (R1.x...
The Issue: Philips Azurion and Allura systems configured with a 1 Phase Uninterruptible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura System configured with a 1 Phase UPS. Allura family (R1.x...
The Issue: Philips Azurion and Allura systems configured with a 1 Phase Uninterruptible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Interventional Fluoroscopic X-Ray System - Philips Allura Xper Series....
The Issue: Potential that a component (air baffle) may be missing in some Nehalem...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed ViewFlex Xtra ICE Catheter to visualize cardiac structures...
The Issue: Specific lots of reprocessed electrophysiology and ultrasound catheters may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed ACUSON AcuNav Ultrasound Catheter for intracardiac and...
The Issue: Specific lots of reprocessed electrophysiology and ultrasound catheters may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Webster CS Catheter 10 Electrodes for electrophysiological...
The Issue: Specific lots of reprocessed electrophysiology and ultrasound catheters may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Inquiry Steerable Diagnostics Catheter for electrogram recording...
The Issue: Specific lots of reprocessed electrophysiology and ultrasound catheters may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Livewire Steerable Electrophysiology Catheter Item Numbers...
The Issue: Specific lots of reprocessed electrophysiology and ultrasound catheters may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: 900-00218 Sterile Cover 10-Pack Shipper Box Assembly Product...
The Issue: The potential of the elastic bands included in the kit detaching or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LinkSymphoKnee System Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due...
The Issue: Some modular LinkSymphoKnee TiNbN Tibial Components were manufactured with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xolair (omalizumab injection) Recalled by Cardinal Health Inc. Due to CGMP...
The Issue: CGMP Deviations - Product was exposed to temperatures outside the product's...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Xolair (omalizumab injection) Recalled by Cardinal Health Inc. Due to CGMP...
The Issue: CGMP Deviations - Product was exposed to temperatures outside the product's...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IMPLANT EPIKUT PLUS MT16 3 Recalled by S.I.N. Implant System Ltda Due to...
The Issue: Dental implants were imported under temperature and storage conditions that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RECOMBINATE Recalled by Cardinal Health Inc. Due to CGMP Deviations -...
The Issue: CGMP Deviations - Product was exposed to temperatures outside the product's...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 4.2% Sodium Bicarbonate Injection Recalled by Exela Pharma Sciences LLC Due...
The Issue: Failed Impurities/Degradation Specifications: out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.