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. 2,384 recalls have been distributed to Alaska in the last 12 months.
Showing 20121–20140 of 46,762 recalls
Recalled Item: OMNIlife science Recalled by OMNIlife science Inc. Due to Acetabular liners...
The Issue: Acetabular liners failed the oxidation testing performed prior to release....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OMNIlife science Recalled by OMNIlife science Inc. Due to Acetabular liners...
The Issue: Acetabular liners failed the oxidation testing performed prior to release....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OMNIlife science Recalled by OMNIlife science Inc. Due to Acetabular liners...
The Issue: Acetabular liners failed the oxidation testing performed prior to release....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Folate 100 test kit-for IVD of folate Recalled by...
The Issue: Homocysteine Assay May Cause Elevated Results in the Folate Assay
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Folate (500 Test Kit)-for IVD of folate Recalled by...
The Issue: Homocysteine Assay May Cause Elevated Results in the Folate Assay
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Folate (500 Test Kit )- for IVD Recalled by Siemens...
The Issue: Homocysteine Assay May Cause Elevated Results in the Folate Assay
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dynex DSX Software-IVD ELISA Assays effected as follows: DSX Assay Recalled...
The Issue: Assay files used on the open Dynex DSX Instrument to process IVD ELISA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge MCC Flow i Disposable CO2 absorber Recalled by GETINGE US SALES LLC...
The Issue: Reversed expiration and manufacturing date on the label
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal Enteral Safe Feeding Tubes: a) Recalled by DeRoyal Industries Inc...
The Issue: Certain MED-RX Polyurethane Feeding Tubes are being recalled due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lisinopril and Hydrochlorothiazide Tablets USP Recalled by Lupin...
The Issue: Presence of Foreign Tablets/Capsules: Product complaint received of one...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MONSEL'S (Ferric Subsulfate) Solution Recalled by Dercher Enterprises, Inc.,...
The Issue: Microbial Contamination of Non-Sterile Products and Superpotent Drug: FDA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Stryker Recalled by Stryker Corporation Due to Complaints have been received...
The Issue: Complaints have been received regarding difficulty in removing the driver...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Recalled by Stryker Corporation Due to Complaints have been received...
The Issue: Complaints have been received regarding difficulty in removing the driver...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips 5-Lead Set Recalled by Philips North America, LLC Due to The...
The Issue: The thickness of the connector to the trunk cable on affected limb lead sets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fujifilm FDR Go Plus mobile X-ray system Recalled by Fujifilm Medical...
The Issue: The graphics driver of the FDR Go PLUS might cause the appearance of a Blue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICRO-TEMP LT System Recalled by Cincinnati Sub-Zero Products LLC, a...
The Issue: Updated Manual-Warnigs have been added stating that exceeding 40'C for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Methylergonovine Maleate USP 0.2 mg Tablets a) 12 count (NDC Recalled by...
The Issue: Presence of Foreign Tablet/Capsule; one Promethazine tablet was found in a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Baxter Healthcare Corporation...
The Issue: Lack of Assurance of Sterility: Bags have potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fennel Whole Seed was packaged in a clear plastic bag Recalled by Mountain...
The Issue: Fennel Whole Seed is recalled due to a potential for contamination with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Arrow AGB+ Multi-Lumen CVC Kit-catheter permits venous access to central...
The Issue: Arrow AGB+ Multi-Lumen CVC Kit - lidstock incorrectly states within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.