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. 2,508 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,508 in last 12 months

Showing 1024110260 of 46,762 recalls

Medical DeviceNovember 10, 2022· GE Medical Systems, LLC

Recalled Item: Vivid q N ultrasound. Not marketed in the US. Used Recalled by GE Medical...

The Issue: Potential for batteries that have not been replaced at 2 years, as...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2022· NuVasive Inc

Recalled Item: X-CORE 2 Ti Core Recalled by NuVasive Inc Due to Potential that insert will...

The Issue: Potential that insert will be unable to disengage from the vertebral body...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2022· GE Medical Systems, LLC

Recalled Item: Vivid S6 N ultrasound. Not marketed in the US. Used Recalled by GE Medical...

The Issue: Potential for batteries that have not been replaced at 2 years, as...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2022· GE Medical Systems, LLC

Recalled Item: Vivid i N ultrasound. Not marketed in the US. Used Recalled by GE Medical...

The Issue: Potential for batteries that have not been replaced at 2 years, as...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugNovember 10, 2022· Nephron Sterile Compounding Center LLC

Recalled Item: PF-Labetalol HCl Injection Recalled by Nephron Sterile Compounding Center...

The Issue: CGMP Deviations: Potential for cross contamination due to product carry over.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 10, 2022· Nephron Sterile Compounding Center LLC

Recalled Item: PF-Neostigmine Methylsulfate Injection Recalled by Nephron Sterile...

The Issue: CGMP Deviations: Potential for cross contamination due to product carry over.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 10, 2022· Par Formulations Private Limited

Recalled Item: Phenoxybenzamine Hydrochloride Capsules Recalled by Par Formulations Private...

The Issue: Failed Impurities/Degradation Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 9, 2022· Lannett Company Inc.

Recalled Item: Triamterene and Hydrochlorothiazide Capsules Recalled by Lannett Company...

The Issue: Failed Impurity/Degradation Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugNovember 9, 2022· ICU Medical Inc

Recalled Item: 0.9% Sodium Chloride Injection Recalled by ICU Medical Inc Due to Lack of...

The Issue: Lack of assurance of sterility: Bags have the potential to leak in the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 9, 2022· ImprimisRx NJ

Recalled Item: Timolol-Latanoprost (0.5/0.005%) ophthalmic drops Recalled by ImprimisRx NJ...

The Issue: Subpotent Drug: The batches contain less than 90% of the labeled amount of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 9, 2022· Lannett Company Inc.

Recalled Item: Triamterene and Hydrochlorothiazide Capsules Recalled by Lannett Company...

The Issue: Failed Impurity/Degradation Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: VIDAS CLINICAL VIDAS RUB IGG 60 TESTS Recalled by Biomerieux Inc Due to As...

The Issue: As the temperature and time out of range was exceeded, product performances...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: VITEK 2 REAGENT AST-GN99 TEST KIT 20 CARDS Recalled by Biomerieux Inc Due to...

The Issue: As the temperature and time out of range was exceeded, product performances...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: BIOBALL A.BRASILIENSIS NCPF 2275 550X20 Recalled by Biomerieux Inc Due to As...

The Issue: As the temperature and time out of range was exceeded, product performances...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: ETEST CLINICAL TOBRAMYCIN TM 256 US S30 Recalled by Biomerieux Inc Due to As...

The Issue: As the temperature and time out of range was exceeded, product performances...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: VITEK 2 REAGENT AST-XN15 TEST KIT 20 CARDS Recalled by Biomerieux Inc Due to...

The Issue: As the temperature and time out of range was exceeded, product performances...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: PPM CLINICAL CHROMID STREPTO B US 20 PLT Recalled by Biomerieux Inc Due to...

The Issue: As the temperature and time out of range was exceeded, product performances...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: BIOBALL K.RHIZOPHILA (30X20) Recalled by Biomerieux Inc Due to As the...

The Issue: As the temperature and time out of range was exceeded, product performances...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: VITEK 2 REAGENT AST-GN70 TEST KIT 20 CARDS Recalled by Biomerieux Inc Due to...

The Issue: As the temperature and time out of range was exceeded, product performances...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2022· Biomerieux Inc

Recalled Item: ETEST CLINICAL VANCOMYCIN VA 256 US S30 Recalled by Biomerieux Inc Due to As...

The Issue: As the temperature and time out of range was exceeded, product performances...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing