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. 2,487 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,487 in last 12 months

Showing 1252112540 of 46,762 recalls

DrugMarch 7, 2022· TMC Acquisition LLC dba Tailor Made Compounding

Recalled Item: Testosterone Cypionate/Enanthate 100/100mg/ml Recalled by TMC Acquisition...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 7, 2022· TMC Acquisition LLC dba Tailor Made Compounding

Recalled Item: Methylene Blue Hypotonic Solution Recalled by TMC Acquisition LLC dba Tailor...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 7, 2022· Siemens Medical Solutions USA, Inc.

Recalled Item: Acuson 9vE4 Transducer Recalled by Siemens Medical Solutions USA, Inc. Due...

The Issue: Transducers (component of ultrasound system) may exceed recommended thermal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: syngo.via RT Image Suite upgraded to VB60 running on SOMATOM Recalled by...

The Issue: Upgraded software version makes an automatic change in laser configuration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: syngo.via RT Image Suite upgraded to VB60 running on syngo.via Recalled by...

The Issue: Upgraded software version makes an automatic change in laser configuration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: syngo.via RT Image Suite upgraded to VB60 running on SOMATOM Recalled by...

The Issue: Upgraded software version makes an automatic change in laser configuration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: syngo.via RT Image Suite upgraded to VB60 running on SOMATOM Recalled by...

The Issue: Upgraded software version makes an automatic change in laser configuration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS SOMATOM with software syngo CT VA30A_SP4 Models: SOMATOM go.Now...

The Issue: Software error may result in sporadic problems causing scanning workflow...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: YSIO X.Pree Recalled by Siemens Medical Solutions USA, Inc Due to For the...

The Issue: For the automated multi-image-acquisition procedure Ortho x-ray collimation...

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

Class II — Potential Health HazardOngoing
DrugMarch 4, 2022· Fagron, Inc

Recalled Item: Nandrolone Decanoate Recalled by Fagron, Inc Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugMarch 4, 2022· Fagron, Inc

Recalled Item: Nandrolone Decanoate Recalled by Fagron, Inc Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugMarch 4, 2022· Fagron, Inc

Recalled Item: Nandrolone Decanoate Recalled by Fagron, Inc Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugMarch 4, 2022· Fagron, Inc

Recalled Item: Nandrolone Decanoate Recalled by Fagron, Inc Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugMarch 4, 2022· Fagron, Inc

Recalled Item: SyrSpend SF Suspending Base Recalled by Fagron, Inc Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Product: Product is contaminated with...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 4, 2022· Fagron, Inc

Recalled Item: Nandrolone Decanoate Recalled by Fagron, Inc Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugMarch 4, 2022· Fresenius Kabi USA, LLC

Recalled Item: Sodium Acetate Injection Recalled by Fresenius Kabi USA, LLC Due to Presence...

The Issue: Presence of particulate matter: particulates composed of carbon and oxygen...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 4, 2022· Swanson Health Products, Inc

Recalled Item: Swanson Ultra: Vitamin B12 Methylcobalamin High Absorption 60 serving per...

The Issue: Dietary supplement may contain potential metal shavings greater than or...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 4, 2022· SML Distribution, LLC

Recalled Item: Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold)...

The Issue: The product was distributed without FDA authorization or clearance for...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 4, 2022· Draegar Medical Systems, Inc.

Recalled Item: Drager Infinity CentralStation Software versions VG2.1.2 and VG2.1.2 SU12....

The Issue: Software issue resulting in temporary loss of central monitoring functionality.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2022· GE Healthcare, LLC

Recalled Item: GE Healthcare MR Systems Recalled by GE Healthcare, LLC Due to During the...

The Issue: During the de-installation of an MR system magnet, if all rigging and...

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

Class II — Potential Health HazardOngoing