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. 2,374 recalls have been distributed to Alaska in the last 12 months.
Showing 22981–23000 of 46,762 recalls
Recalled Item: DeltaVision OMX SR Imaging System Model Number: 29115476 The DeltaVision...
The Issue: Non-conformance with the DeltaVision OMX SR, the interlocks are not wired in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Knee Instruments Disposable Fluted Headless Pins Recalled by...
The Issue: Potential for outer pouch sterile barrier to be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V-Twin Recalled by Vital Scientific N.V. Due to The action is being...
The Issue: The action is being initiated because the cooling indicator board was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codan Filter (Codan catalog number BC 693) used with Medrad Recalled by...
The Issue: Bayer has received reports of loose particulate in the filter when the dust...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Lipase Flex Reagent Cartridge Recalled by Siemens Healthcare...
The Issue: There is lot to lot variability for QC and patient results when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Lipase Flex Reagent Cartridge Recalled by Siemens Healthcare...
The Issue: There is lot to lot variability for QC and patient results when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minivelle (estradiol transdermal system) Patches Recalled by Noven...
The Issue: Defective Delivery System: out of specification results for shear, an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Minivelle (estradiol transdermal system) Patches Recalled by Noven...
The Issue: Defective Delivery System: out of specification results for shear, an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Minivelle (estradiol transdermal system) Patches Recalled by Noven...
The Issue: Defective Delivery System: out of specification results for shear, an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Minivelle (estradiol transdermal system) Patches Delivers 0.1 mg/day...
The Issue: Defective Delivery System: out of specification results for shear, an...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pramipexole dihydrochloride extended release tablets Recalled by Par...
The Issue: Failed impurities/degradation specifications: Finished product contain a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection USP 50 mL Viaflex container Baxter Recalled...
The Issue: cGMP Deviation
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bupropion Hydrochloride ER Tablets Recalled by InvaGen Pharmaceuticals, Inc....
The Issue: Failed impurities/ degradation specifications: Out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CryoPatch SG Pulmonary Hemi-Artery Recalled by CryoLife, Inc. Due to The...
The Issue: The conduit length and branch length of a SG Pulmonary Hemi-Artery were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Altrix¿ Precision Temperature Management System Model: 8001Product Usage:...
The Issue: Users may experience alarm fatigue due to frequent alarming relating to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heating Profile PRISMAFLO II blood return warmer for Prismaflex Product...
The Issue: PRISMAFLO II and PRISMAFLO II S Heating Profile only and not the Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heating Profile PRISMAFLO II S blood return warmer for Prismaflex Recalled...
The Issue: PRISMAFLO II and PRISMAFLO II S Heating Profile only and not the Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heating Profile PRISMAFLO II S blood return warmer for Prismaflex Recalled...
The Issue: PRISMAFLO II and PRISMAFLO II S Heating Profile only and not the Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray Blood Culture Identification (BCID) Recalled by BioFire...
The Issue: Increased risk of false positive results for Proteus when the product is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis POWERFLEX PRO PTA Dilatation Catheter - Product Usage: Is Recalled by...
The Issue: Product may not meet the internal manufacturing shaft subassembly burst...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.