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. 2,245 recalls have been distributed to Alaska in the last 12 months.
Showing 45701–45720 of 46,762 recalls
Recalled Item: ABL80 FLEX (with FLEX software) and ABL80 FLEX CO-OX (with Recalled by Sendx...
The Issue: The firm recalled because the glucose measurements from a patient sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Rigid Suction Wand Recalled by Edwards Lifesciences,...
The Issue: Edwards is recalling Suction Wand models SPC2081 and S033 because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kombiglyze XR (saxagliptin and metformin HCl extended-release) tablets...
The Issue: Labeling; Correct labeled product miscart/mispack: Some Physician sample...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kombiglyze XR (saxagliptin and metformin HCl extended-release) tablets...
The Issue: Labeling; Correct labeled product miscart/mispack: Some Physician sample...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Caziant (desogestrel and ethinyl estradiol) Tablets Recalled by Watson...
The Issue: Impurities/Degradation Products: High Out-of-specification results were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pitocin (Oxytocin Injection Recalled by JHP Pharmaceuticals, LLC Due to...
The Issue: Labeling: Label Mix-up: Pitocin storage conditions should be labeled, "Store...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Campbell's Oyster Stew Recalled by Campbell Soup Supply Co., LLC Due to The...
The Issue: The product has been prepared, packed, or held under insanitary conditions...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PathFinder NXT Pivoting Percutaneous Rod Holder This device is an Recalled...
The Issue: Complaints have been reported where, during surgery, the surgeon was unable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pathfinder NXT Fixed Percutaneous Rod Holder Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer is recalling Pathfinder NXT Fixed Percutaneous Rod Holder, because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Button Switchpens Recalled by PSC Industries Inc Due to The carton label for...
The Issue: The carton label for this device has the manufacturer symbol where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Button Switchpens Recalled by PSC Industries Inc Due to The Tyvek pouch...
The Issue: The Tyvek pouch label for this device states: 'with holster'; however, this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pathfinder NXT Fixed Percutaneous Rod Holder Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer is recalling Pathfinder NXT Fixed Percutaneous Rod Holder, because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trizivir (abacavir sulfate 300mg Recalled by GlaxoSmithKline Inc Due to...
The Issue: Adulterated Presence of Foreign Tablets: Trizivir 300/150/300 mg tables, Lot...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Product is a liquid dietary supplement packaged in white plastic Recalled by...
The Issue: Product ("Digestive 3 in 1 Health") was manufactured using a raw ingredient...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Aesculap(R) - Miethke Shunt System Recalled by Aesculap, Inc. Due to The...
The Issue: The deflector may not move freely on the ventricular catheter. The deflector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica M525 F50 Surgical Microscope Recalled by Leica Microsystems, Inc. Due...
The Issue: Leica Microsystems evaluated data showing that a malfunction resulting in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARDIOGEN-82 (Rubidium Rb 82 Generator) Recalled by Bracco Diagnostics Inc...
The Issue: GMP deviation; Sr-82 levels exceeded alert limit specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clams Recalled by Rhee Brothers Incorporated Due to Frozen clams, product of...
The Issue: Frozen clams, product of S. Korea, may be contaminated with Norovirus.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: I-Flow ON-Q Pain Relief System Recalled by I-Flow LLC Due to I-Flow...
The Issue: I-Flow initiated two voluntary product removals of the ON-Q Pain Relief...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: I-Flow ON-Q Pain Relief System Recalled by I-Flow LLC Due to I-Flow...
The Issue: I-Flow initiated two voluntary product removals of the ON-Q Pain Relief...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.