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. 961 recalls have been distributed to Alaska in the last 12 months.
Showing 29721–29740 of 46,762 recalls
Recalled Item: DMAA (1 Recalled by NATURECOM INC Due to Naturecom dba NutriVitaShop is...
The Issue: Naturecom dba NutriVitaShop is recalling DMAA net weight 500 g because there...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Green Dirt Farm "Dirt Lover" sheep's milk cheese packaged in cases of 8...
The Issue: Product is contaminated with Staphylococcus aureus exceeding action limit of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Plush Puffs Marshmallows Toasty Coconut 4oz. and 2lb bulk bag Recalled by To...
The Issue: Undeclared allergen of milk from the declared ingredient coconut cream powder.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PROTONIX I.V. (pantoprazole sodium) for Injection Recalled by Pfizer Inc....
The Issue: Subpotent Drug: Out of Specification (OOS) for potency at the 6-month...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Toms of Maine Naturally Dry Natural Powder Antiperspirant Stick Recalled by...
The Issue: Labeling: Label Mix Up- Incorrect back label applied to the product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SIEMENS IMMULITE 2000/2000 Xpi Systems Intact PTH (Parathyroid Hormone) Test...
The Issue: Siemens is conducting this recall for the IMMULITE¿ 2000/IMMULITE¿ 2000 XPi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Savannah-T Straight Rod Recalled by Amendia, Inc Due to The rods are...
The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Recalled by Teleflex Medical Due to Labeling Inconsistency: The...
The Issue: Labeling Inconsistency: The products have been labeled with the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Stylet Needle Recalled by Amendia, Inc Due to The rods are packaged in...
The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Black Widow 6.6mm x 20mm Screw Recalled by Amendia, Inc Due to There is a...
The Issue: There is a problem with the mating feature between the plate and screw which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyberKnife Robotic Radiosurgery System using software version 10.6 Recalled...
The Issue: Accuray has become aware of a potential safety issue involving unexpected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-Wire 1.4mm x 12in Non-Threaded Recalled by Amendia, Inc Due to The rods...
The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G3 Opticage Expandable Interbody Fusion Device Recalled by Interventional...
The Issue: During implantation, the proximal end of the device could separate if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Black Widow Plate 19mm Plate Recalled by Amendia, Inc Due to There is a...
The Issue: There is a problem with the mating feature between the plate and screw which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Durex Pleasure Pack . 3 ultra fine lubricated latex condoms Recalled by...
The Issue: Reckitt Benckiser LLC is recalling Durex Condoms Pleasure Packs due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ceramax Skin Barrier Cream: NET WT 0.1 OZ (3 g Recalled by Oculus Innovative...
The Issue: Firm became aware that professional samples of Ceramax are not meeting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GalaSHAPE 3D Recalled by Tepha Incorporated Due to Endotoxin values from...
The Issue: Endotoxin values from testing of retains slightly exceeded the established...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Giraffe Incubator The Giraffe Incubator is an infant incubator. Incubators...
The Issue: Certain power cords could overheat. The affected power cords were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FV-RF (Clinix RF Plus) Product Usage: A Stationary X-ray System Recalled by...
The Issue: There's a potential for liquid penetration into the back side of the front...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000/IMMULITE 2000 XPi Systems Prostate-Specific Antigen (PSA)...
The Issue: Siemens Healthcare Diagnostics confirmed that the IMMULITE 2000/ IMMULITE...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.