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. 2,258 recalls have been distributed to Alaska in the last 12 months.
Showing 43041–43060 of 46,762 recalls
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RigiflexTM 11 Single-Use Achalasia Balloon Dilator Recalled by Boston...
The Issue: Product labeled with incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD PERIPHERAL VASCULAR VACCESS¿ PTA Balloon Dilatation Catheters Recalled...
The Issue: Bard Peripheral Vascular (BPV) has confirmed that some product code/lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NephroMax high Pressure nephrostomy Balloon Catheter Kit. Material...
The Issue: Incorrect sized renal sheath was packaged with the NephroMax high pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VenaFlow Elite 30B-B and 30BI-B Product Usage: The VenaFlow Elite Recalled...
The Issue: DJO, LLC has recently identified a product safety issue with the battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NephroMax high Pressure Nephrostomy Balloon Catheter. Material...
The Issue: Incorrect sized renal sheath was packaged with the NephroMax high pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SL & SLi Series (Mod 15/18/20/25) Linear Accelerator Used for Recalled by...
The Issue: Customers are resetting the default values outside recommended factory settings.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...
The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAR S3 ActiveTrack Excimer System (STAR S3) Mfg by AMO Manufacturing USA...
The Issue: Under specific conditions, there is an unlikely potential to result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alair Bronchial Thermoplasty Catheter Recalled by Boston Scientific...
The Issue: Boston Scientific has discovered an inconsistent "Use By" expiration date on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYNCHRON System(s) Lactate (LACT) Reagent. Product Usage: Lactate (LACT)...
The Issue: Beckman Coulter has confirmed customer reports of LACT Lot M210077 failing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAR S4 with Variable Spot Scanning Excimer System (STAR S4) Recalled by...
The Issue: Under specific conditions, there is an unlikely potential to result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINUTE MAID CRANBERRY APPLE RASPBERRY Flavored Juice Beverage Recalled by...
The Issue: Products with the specific Lot Code and Codes listed above are being...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MINUTE MAID ORANGE JUICE Recalled by Coca-Cola USA, Inc. Due to Products...
The Issue: Products with the specific Lot Code and Codes listed above are being...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MINUTE MAID STRAWBERRY PASSION Flavored Juice Beverage Recalled by Coca-Cola...
The Issue: Products with the specific Lot Code and Codes listed above are being...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MINUTE MAID Mixed Berry Juice Recalled by Coca-Cola USA, Inc. Due to...
The Issue: Products with the specific Lot Code and Codes listed above are being...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MINUTE MAID APPLE JUICE Recalled by Coca-Cola USA, Inc. Due to Products with...
The Issue: Products with the specific Lot Code and Codes listed above are being...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Eyebright Concentrate Topical Eye Rinse Recalled by Earthlabs, Inc. DBA Wise...
The Issue: Lack of Assurance of Sterility; Lack of Assurance of Sterility; product not...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Propofol Injectable Emulsion Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter; single visible particulate was identified...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.