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 43861–43880 of 46,762 recalls
Recalled Item: The LifeCare Pump Model 4200 PCA Infuser makes possible the Recalled by...
The Issue: Hospira has received reports of PCA pumps not detecting distal occlusions,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeCare PCA infusion system with Hospira MedNet software allows clinicians...
The Issue: Hospira has received reports of PCA pumps not detecting distal occlusions,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 3.5 MM LCP(R) Distal Humerus System The Synthes 3.5 Recalled by...
The Issue: Recall is being initiated due to the part being mislabeled (Part Number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Midfoot Fusion Bolt 6.5 mm. It is indicated for fracture Recalled by...
The Issue: A post market safety review following several customer complaints indicated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDICYCL-E- Lite Portable Oxygen System An integrated portable oxygen...
The Issue: A number of MEDICYL-e Portable Oxygen Systems may have misapplied valve flow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APLIF Implants and Instruments Recalled by Spinal Solutions, LLC Due to...
The Issue: Spinal Solutions is recalling the APLIF system because it is not supported...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bracket Buccal Tube U7L DB/UL22 Roth MT HK 0/-14/0 Product Recalled by...
The Issue: Ormco Corporation is voluntarily recalling one (1) lot of Bracket Buccal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Systems with Software Artis VC20x/VC21A/VD10x that have a DSA Recalled...
The Issue: The firm has become aware of a potential issue on Artis systems with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rifadin Recalled by Sanofi US Due to Subpotent drug: low fill volume in some...
The Issue: Subpotent drug: low fill volume in some of the capsules
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 4 way Saline Moisturizing Mist with Eucalyptol & Menthol Recalled by...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date. The lot number and/or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nupercainal Recalled by Novartis Consumer Health Due to Labeling: Incorrect...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date. The lot number and/or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 4 way Nasal Decongestant Menthol Nasal Spray Recalled by Novartis Consumer...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date. The lot number and/or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 4 way Nasal Decongestant Fast Acting Nasal Spray Recalled by Novartis...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date. The lot number and/or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Myoflex (trolamine salicylate) 10% Recalled by Novartis Consumer Health Due...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date. The lot number and/or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Maquet Getinge Group battery modules for use with Maquet SERVO-i Recalled by...
The Issue: When using the SERVO-i on battery power, in a very small number of cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAQUET CARDIOHELP Support System: CARDIOHELP-I Software (up to version...
The Issue: It has come to the attention of MAQUET that there have been episodes of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torrent" irrigation tubing. Product Usage: The Torrent irrigation system...
The Issue: The firm was notified by their customers that there was a water leakage from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advanced Orthogonal Percussion Adjusting Instrument Indicated for use by a...
The Issue: Unapproved medical device
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Healthcare Diagnostics Inc. MIcroScan MICroSTREP plus Type 1...
The Issue: Customer complaint investigation confirmed the issue of false skipped wells...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Alere Cholestech LDX¿ high sensitivity C-Reactive Protein (hsCRP) Test...
The Issue: The Alere Cholestech LDX¿ hsCRP cassette (PN 12-807) may have increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.