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. 1,027 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
1,027 in last 12 months

Showing 15881–15900 of 46,762 recalls

Medical DeviceDecember 18, 2020· Hill-Rom, Inc.

Recalled Item: Liko Multirall 200 overhead lift- overhead lift is a general-purpose...

The Issue: Multirall Q-link strap lock has not been fully engaged in the S65 rail...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 18, 2020· Alung Technologies Inc

Recalled Item: ALung Technologies Hemolung Respiratory Assist System (RAS) with CME...

The Issue: CME America BodyGuard 323 Infusion Pumps (recalled by manufacturer) is a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2020· Laerdal Medical (Suzhou) Co., Ltd.

Recalled Item: Laerdal Compact Suction Unit (LCSU 4) Recalled by Laerdal Medical (Suzhou)...

The Issue: Component failures may cause the unit to lose all suction. Users will need...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2020· Ansh Labs, LLC

Recalled Item: AnshLabs - SARS-CoV2 IgM ELISA (u-Capture) Recalled by Ansh Labs, LLC Due to...

The Issue: Labeling update; To reduce the risk of false positive/false negative results...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS Icono biplane Model:11327600 ARTIS Icono floor system Model: 11327700...

The Issue: Misleading error messages and a gap in the Operator Manual which affects...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2020· Bioventus, LLC

Recalled Item: EXOGEN Ultrasound Coupling Gel Recalled by Bioventus, LLC Due to Product may...

The Issue: Product may contain white particulates that are microbial in nature.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2020· GE Healthcare, LLC

Recalled Item: System Recalled by GE Healthcare, LLC Due to GE Healthcare has become aware...

The Issue: GE Healthcare has become aware of a potential issue on Revolution Apex,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2020· Roche Diagnostics Operations, Inc.

Recalled Item: A calculator/data processing module for clinical use is an electronic...

The Issue: A software error results in the unintentional removal of the serum-indices...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2020· GE Healthcare, LLC

Recalled Item: System Recalled by GE Healthcare, LLC Due to GE Healthcare has become aware...

The Issue: GE Healthcare has become aware of a potential issue on Revolution Apex,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2020· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius Medical Care NaturaLyte Liquid Acid concentrate-Liquid Acid...

The Issue: Bottles Missing Product Label

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

Class II — Potential Health HazardOngoing
DrugDecember 17, 2020· SCA Pharmaceuticals

Recalled Item: neostigmine methylsulfate 5 mg/5 mL Recalled by SCA Pharmaceuticals Due to...

The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2020· SCA Pharmaceuticals

Recalled Item: Lidocaine HCl 1% 10 mL (10mg/ml) Recalled by SCA Pharmaceuticals Due to Lack...

The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2020· SCA Pharmaceuticals

Recalled Item: Atropine Sulfate Injection Recalled by SCA Pharmaceuticals Due to Lack of...

The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2020· SCA Pharmaceuticals

Recalled Item: fentaNYL 100 mcg/2mL Injection for IV or IM Use Recalled by SCA...

The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2020· SCA Pharmaceuticals

Recalled Item: Glycopyrrolate 1 mg/5mL (0.2mg/mL) Recalled by SCA Pharmaceuticals Due to...

The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2020· SCA Pharmaceuticals

Recalled Item: morphine sulfate 150 mg/30 mL in 0.9% Sodium Chloride Injection Recalled by...

The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2020· SCA Pharmaceuticals

Recalled Item: ePHEDrine Sulfate Recalled by SCA Pharmaceuticals Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2020· SCA Pharmaceuticals

Recalled Item: Sodium Citrate 4% 3 mL Anticoagulation Solution (40mg/mL) Recalled by SCA...

The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2020· SCA Pharmaceuticals

Recalled Item: fentaNYL 100 mcg/50mL Ropivacaine HCl 0.1% in 0.9% Sodium Chloride 50 mL...

The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2020· SCA Pharmaceuticals

Recalled Item: ePHEDrine 25 mg/5 mL in 0.9% Sodium Chloride Injection Recalled by SCA...

The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...

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

Class II — Potential Health HazardOngoing
Refund