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. 2,326 recalls have been distributed to Alaska in the last 12 months.
Showing 34501–34520 of 46,762 recalls
Recalled Item: Carto 3 EP Navigation System. Electro physiology system which views Recalled...
The Issue: Image disappeared from the cardiac ultrasound system when the CARTO 3 EP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 6.5 mm Recalled...
The Issue: Sterility of device is compromised due to breach in the packaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ClomiPHENE CITRATE Tablets Recalled by EMD Serono, Inc. Due to Chemical...
The Issue: Chemical Contamination: impurity failure due to chemical contamination of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All Products Intended to be Sterile Recalled by Medistat RX L.L.C. Due to...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bravelle 75 IU (urofollitropin for injection Recalled by Ferring...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ARCHITECT i2000SR System The Abbott ARCHITECT System is intended for...
The Issue: Incorrect tubing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluorescence Imaging Procedure Kits used with the da Vinci Si Recalled by...
The Issue: B. Braun 2 gang 4-way stopcocks in the Fluorescence Imaging Procedure Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prism Medical P-300 Portable Consumer Lift Recalled by ErgoSafe Products,...
The Issue: Drive shaft and over speed arm may simultaneously fail potentially resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prism Medical C-300 Consumer Ceiling Lift Recalled by ErgoSafe Products, LLC...
The Issue: Drive shaft and over speed arm may simultaneously fail potentially resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker UniVise Spinous Process Fixation Plate System Inserter Recalled by...
The Issue: The Inserter Inner Shaft would not fit through the Inserter. The inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Tapers LFIT V40 Vitallium femoral heads. hip prosthesis...
The Issue: Complaints that the femoral head could not be assembled with its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Family Gourmet Natural Whole Grain Brown Rice Recalled by Family Dollar...
The Issue: Live insects were noted inside several unopened bags of product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Family Gourmet Long Grain Enriched White Rice Recalled by Family Dollar...
The Issue: Live insects were noted inside several unopened bags of product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 5.0mm Unit Rod 270mm Recalled by Synthes (USA) Products LLC Due to This...
The Issue: This product was produced using a finishing process not identified as part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EnVision FLEX/HRP visualization reagent found in the following kits:...
The Issue: There is a defect in one lot of a buffer, non-specific background staining...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fenoglide (fenofibrate) tablets Recalled by Valeant Pharmaceuticals North...
The Issue: Failed Dissolution Specifications: Failed 24 month dissolution testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Surgicept (Ethyl alcohol 70% w/w) WATERLESS Surgical Hand Scrub & Recalled...
The Issue: Chemical Contamination: Naphthalene compound identified in the product after...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 3-Day Cleanse Recalled by TN Juice Bar Due to Unpasteurized juice product...
The Issue: Unpasteurized juice product with elevated pH levels and unlabeled almond...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Novocastra Lyophilized Mouse Monoclonal Antibody CD10 (CD10)....
The Issue: These Lot numbers are not stable up to the expiry date on the product labeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BAUSCH + LOMB Biotrue ONEday lenses (nesofilcon A) Recalled by Bausch & Lomb...
The Issue: The firm determined that 25 lots had been manufactured with a minor surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.