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. 1,057 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
1,057 in last 12 months

Showing 7581–7600 of 46,762 recalls

Medical DeviceSeptember 6, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008T Hemodialysis System without CDX Recalled by Fresenius Medical Care...

The Issue: Potential PCBA leaching from tubing of hemodialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 6, 2023· Beckman Coulter Biomedical Division

Recalled Item: AU/DxC AU Chemistry Transferrin Immune complexes formed in Recalled by...

The Issue: The firm has identified that the Transferrin reagent does not meet the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2023· CareFusion 303, Inc.

Recalled Item: BD Pyxis CII Safe ES Recalled by CareFusion 303, Inc. Due to When global...

The Issue: When global edit is used to update multiple formulary properties...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2023· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008T HD SYS. CDX BLUESTAR Recalled by Fresenius Medical Care Holdings, Inc....

The Issue: Potential PCBA leaching from tubing of hemodialysis machines.

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 6, 2023· GE MEDICAL SYSTEMS, ISRAEL LTD.

Recalled Item: Venue Go Standard Carts Ref: (H45181VC and H45103VCW) Recalled by GE MEDICAL...

The Issue: Some Venue Go Standard Carts can develop an internal failure of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2023· Getinge Usa Sales Inc

Recalled Item: Meera Mobile Operating Table-to support and position the patient immediately...

The Issue: Under certain conditions, an issue might prevent the device from performing...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2023· Zimmer Surgical Inc

Recalled Item: Zimmer Dermatome Blades- 10-pack boxes of blades. Intended for use Recalled...

The Issue: Skin grafts thin and non-uniform when using the affected blades. The issue...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2023· Mazor Robotics Ltd

Recalled Item: MAZOR X robotic guidance system Recalled by Mazor Robotics Ltd Due to...

The Issue: Software update

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

Class II — Potential Health HazardOngoing
DrugSeptember 5, 2023· BE PHARMACEUTICALS AG

Recalled Item: Pantoprazole Sodium for Injection 40mg per vial Recalled by BE...

The Issue: Lack of Assurance of Sterility: Powder discoloration due to small crack in...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2023· Amerisource Health Services LLC

Recalled Item: HydrALAZINE Hydrochloride Tablets Recalled by Amerisource Health Services...

The Issue: Failed Impurities/Degradation Specifications: Out of Specification results...

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 1, 2023· American Contract Systems, Inc.

Recalled Item: Vasc. Open CVOR SJH Recalled by American Contract Systems, Inc. Due to...

The Issue: During an internal investigation, ACS identified that the components, I.V....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· Siemens Medical Solutions USA, Inc

Recalled Item: (1) Over-ear headphones used with the MAGNETOM Amira MAGNETOM Free.Star...

The Issue: In some cases, when lubricating grease is present within the headband of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· American Contract Systems, Inc.

Recalled Item: General Pack Recalled by American Contract Systems, Inc. Due to During an...

The Issue: During an internal investigation, ACS identified that the components, I.V....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· American Contract Systems, Inc.

Recalled Item: Robotics Pack Recalled by American Contract Systems, Inc. Due to During an...

The Issue: During an internal investigation, ACS identified that the components, I.V....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· American Contract Systems, Inc.

Recalled Item: Sub Q Recorder Pack Recalled by American Contract Systems, Inc. Due to...

The Issue: During an internal investigation, ACS identified that the components, I.V....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· Convergent Dental

Recalled Item: Solea Models 2.0 and 3.0 Laser Surgical Instrument Recalled by Convergent...

The Issue: It has been found that potential unintended laser activation can occur...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· American Contract Systems, Inc.

Recalled Item: Robotics Pack Recalled by American Contract Systems, Inc. Due to During an...

The Issue: During an internal investigation, ACS identified that the components, I.V....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· American Contract Systems, Inc.

Recalled Item: Cath Cardiac Pack Recalled by American Contract Systems, Inc. Due to During...

The Issue: During an internal investigation, ACS identified that the components, I.V....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· American Contract Systems, Inc.

Recalled Item: Breast Plastics Pack Recalled by American Contract Systems, Inc. Due to...

The Issue: During an internal investigation, ACS identified that the components, I.V....

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· American Contract Systems, Inc.

Recalled Item: Pediatric Urology Wolson Pack Recalled by American Contract Systems, Inc....

The Issue: During an internal investigation, ACS identified that the components, I.V....

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

Class II — Potential Health HazardOngoing