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. 2,508 recalls have been distributed to Alaska in the last 12 months.
Showing 9501–9520 of 46,762 recalls
Recalled Item: PCRopsis Support: a) 1 mL Recalled by Entopsis , Inc. Due to Presence of...
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis Reagent RVD-RT Recalled by Entopsis , Inc. Due to Presence of...
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis Activator: a) 1.5mL Recalled by Entopsis , Inc. Due to Presence of...
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis Reagent Buccal Recalled by Entopsis , Inc. Due to Presence of...
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPerfusion Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: There are technical issues related to signal generation and processing,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2D Perfusion Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to There...
The Issue: There are technical issues related to signal generation and processing,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Moberg Component Neuromonitoring System (CNS Monitor)-Intended as a...
The Issue: Battery leakage can cause corrosion to the metal enclosure near the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENFAMIL PROSOBEE PWD 12.9OZ (6CAN) US Recalled by Mead Johnson & Company Due...
The Issue: Reckitt, a producer of nutrition products, announced today that out of an...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DIBUCAINE 1% HEMORRHOIDAL OINTMENT Recalled by Akron Pharma, Inc. Due to...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gabapentin Tablets Recalled by Sciegen Pharmaceuticals Inc Due to Presence...
The Issue: Presence of Foreign Tablets/Capsules: Pharmacist reported presence of some...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Stainless Steel Water Bottle The product comes in four sizes: 32 oz....
The Issue: Water bottle has a cup with a screw cap attached by a weld that has been...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Agilent Resolution ctDx FIRST Sample Collection Kit Recalled by AGILENT...
The Issue: Distributed sample collection kit with an unapproved instruction for use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Raystation treatment planning system for radiation therapy Recalled by...
The Issue: It is possible to set a non-zero collimator angle in the Virtual Simulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...
The Issue: Incorrect type of titanium was used which reduces the gripping strength of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...
The Issue: Incorrect type of titanium was used which reduces the gripping strength of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...
The Issue: Incorrect type of titanium was used which reduces the gripping strength of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...
The Issue: Incorrect type of titanium was used which reduces the gripping strength of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFINITY Occipitocervical Upper Thoracic System Recalled by Medtronic...
The Issue: Incorrect type of titanium was used which reduces the gripping strength of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Testosterone Cypionate Injection Recalled by Azurity Pharmaceuticals, Inc....
The Issue: cGMP: complaints of crystals not redissolving into solution after warming...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Buprenorphine Transdermal System Recalled by AVEVA Drug Delivery Systems,...
The Issue: Failed Impurities/Degradation Specifications: Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.