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. 2,440 recalls have been distributed to Alaska in the last 12 months.
Showing 17441–17460 of 46,762 recalls
Recalled Item: Aripiprazole Tablets Recalled by Alembic Pharmaceuticals Limited Due to...
The Issue: Labeling: Label mix up: Bottles labeled as aripiprazole 2 mg, 30 count had...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nystatin Cream Recalled by Crown Laboratories Due to Subpotent Drug: Out of...
The Issue: Subpotent Drug: Out of specification for assay at the 9-month interval for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nuvasive NVM5 EMG Module Recalled by NuVasive Inc Due to The NVM5 EMG Module...
The Issue: The NVM5 EMG Module kit intended for intraoperative neurophysiologic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Expansion Control Overlay Recalled by EHOB, Inc. Due to QC inspection...
The Issue: QC inspection observed that a portion of the lot may have been contaminated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enVista one-piece hydrophobic acrylic toric intraocular lens Recalled by...
The Issue: The toric axis marks were misaligned (from the expected position in relation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.8mm Truss Wire Recalled by New Standard Device Inc Due to 1.8mm truss...
The Issue: 1.8mm truss wires are being removed to facilitate the introduction of 2.0mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accurian RF Ablation Recalled by Medtronic Sofamor Danek USA Inc Due to...
The Issue: Insertion difficulty of the probes. The probe was catching on a lip inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accurian RF Ablation Recalled by Medtronic Sofamor Danek USA Inc Due to...
The Issue: Insertion difficulty of the probes. The probe was catching on a lip inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accurian RF Ablation Recalled by Medtronic Sofamor Danek USA Inc Due to...
The Issue: Insertion difficulty of the probes. The probe was catching on a lip inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accurian RF Ablation Recalled by Medtronic Sofamor Danek USA Inc Due to...
The Issue: Insertion difficulty of the probes. The probe was catching on a lip inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accurian RF Ablation Recalled by Medtronic Sofamor Danek USA Inc Due to...
The Issue: Insertion difficulty of the probes. The probe was catching on a lip inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accurian RF Ablation Recalled by Medtronic Sofamor Danek USA Inc Due to...
The Issue: Insertion difficulty of the probes. The probe was catching on a lip inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACTIV.A.C Therapy System Recalled by KCI USA, INC. Due to The device may...
The Issue: The device may power off without notification to the user resulting in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips M3015A Microstream CO2 Extension Model No. 862393 -used with...
The Issue: Affected M3015A extensions are incompatible with the lntelliVue X3 Patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lokomat Pro Recalled by Hocoma AG Due to The motor controller may fail,...
The Issue: The motor controller may fail, which can potentially lead to an error in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Time-Cap Labs Recalled by Marksans Pharma Limited Due to CGMP Deviations:...
The Issue: CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prednisolone Sodium Phosphate Oral Solution Recalled by Akorn, Inc. Due to...
The Issue: Discoloration: Out of Specification (OOS) result for APHA Color Test.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: STAT KIT Z-1000 emergency medical kit HealthFirst - Product Usage: Recalled...
The Issue: A missing component (hand suction pump) in the emergency medical kits.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StealthStation" S7 System with Polaris Spectra Camera part number PSU...
The Issue: There is a potential for specific camera units to be affected by a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OrthoPediatrics ACL Reconstruction System ShieldLoc 7mm implant component...
The Issue: ShieldLoc implant component of the ACL Reconstruction Systemlots may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.