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. 2,251 recalls have been distributed to Alaska in the last 12 months.
Showing 45221–45240 of 46,762 recalls
Recalled Item: ProBalance Protein To Go(TM) Recalled by Protica, Inc Due to Product not...
The Issue: Product not sufficiently acidified (equilibrium pH higher than 4.6),...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Protein Shots Recalled by Protica, Inc Due to Product not sufficiently...
The Issue: Product not sufficiently acidified (equilibrium pH higher than 4.6),...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Protein Wave 15 grams of protein Recalled by Protica, Inc Due to Product not...
The Issue: Product not sufficiently acidified (equilibrium pH higher than 4.6),...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Vital Signs Disposable General Purpose 9 French Temperature Probe For...
The Issue: There is a potential for epistaxis during use of the Disposable General...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Torx 6.5mm Cancellous Bone Screw The Recalled by...
The Issue: Stryker has received reports from the field indicating that certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Torx 6.5mm Cancellous Bone Screw The Recalled by...
The Issue: Stryker has received reports from the field indicating that certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Varian brand Eclipse Treatment Planning System Recalled by Varian Medical...
The Issue: Varian has identified an anomaly with the Eclipse Treatment Planning where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Octopus 101 Perimeter Recalled by Haag-Streit USA Inc Due to The firm...
The Issue: The firm recalled the device after learning of a possible deviation in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luigi's Real Italian Ice Birthday Cake 6 FL OZ cups Recalled by J & J Snack...
The Issue: Luigi's Real Italian Ice Birthday Cake Flavor is mislabeled as "Dairy-Free".
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: KARL STORZ Photodynamic Diagnosis (PDD) D-Light C System Recalled by Karl...
The Issue: The recall was initiated because Karl Storz has confirmed that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll X Series Defibrillator/Pacemaker/Monitor Product Usage: The product is...
The Issue: Shipped with incorrect software
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HYDROmorphone HCl Injection Recalled by Hospira Inc. Due to Superpotent...
The Issue: Superpotent (Single Ingredient) Drug: The prefilled cartridge unit has been...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Capex Shampoo (fluocinolone acetonide) Recalled by Galderma Laboratories,...
The Issue: Subpotent; fluocinolone acetonide.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Stockert Heater-Cooler 3T Recalled by Sorin Group USA, Inc. Due to On August...
The Issue: On August 15, 2012, Sorin informed consignees via letter of changes made to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips SureSigns VSi/VS2+ patient monitors Model Part Numbers VSi/ 863275...
The Issue: Philips SureSigns VSi/VS2+ patient monitors may not be properly secured and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Choletec - Kit for the Preparation of Technetium Tc 99m Mebrofenin Recalled...
The Issue: Presence of Particulate Matter; potential for charcoal particulates
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prometh VC Plain Recalled by Actavis Mid Atlantic LLC Due to...
The Issue: Impurities/Degradation Products: Recalled lots do not meet room temperature...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prometh VC with Codeine Cough Syrup Recalled by Actavis Mid Atlantic LLC Due...
The Issue: Impurities/Degradation Products: Recalled lots do not meet room temperature...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: THERA PEARL 3-in-1 BREAST THERAPY Recalled by Lansinoh Laboratories Inc Due...
The Issue: The Spanish translation on the Instructions for Use (IFU) insert and product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JUGGERKNOT IN¿GUIDE PUNCH Recalled by Biomet, Inc. Due to Investigation...
The Issue: Investigation found that the current design of the product allows the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.