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. 2,480 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,480 in last 12 months

Showing 1344113460 of 27,254 recalls

Medical DeviceMay 3, 2019· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Connect Diabetes Management App Recalled by Roche Diabetes Care,...

The Issue: Users with Android OS 8.0 and above may be unable to transfer values...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2019· Monarch Medical Technologies

Recalled Item: Monarch Medical Technologies EndoTool IV Recalled by Monarch Medical...

The Issue: Insulin dosing calculations were erroneously high.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· Becton Dickinson & Company

Recalled Item: CareFusion MaxPlus Clear Needleless Connector. Intended for Positive...

The Issue: After disconnection of a luer, the valve of the connector remains recessed;...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· SenTec AG

Recalled Item: SenTec Standard Starter Set with and without Service Gas (2 Recalled by...

The Issue: There is an increased chance (approx. 5%) of no electrolyte or a reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· Bard Peripheral Vascular Inc

Recalled Item: EnCor Breast Biopsy Probes Recalled by Bard Peripheral Vascular Inc Due to...

The Issue: There has been an increase in complaints related to leaks, suction issues,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· SenTec AG

Recalled Item: SenTec Membrane Changer (reloadable) [9 pcs] - Product Usage: Is Recalled by...

The Issue: There is an increased chance (approx. 5%) of no electrolyte or a reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· Bard Peripheral Vascular Inc

Recalled Item: EnCor Breast Biopsy Probes Recalled by Bard Peripheral Vascular Inc Due to...

The Issue: There has been an increase in complaints related to leaks, suction issues,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· SenTec AG

Recalled Item: SenTec Neonatal Starter Set with and without Service Gas (2 Recalled by...

The Issue: There is an increased chance (approx. 5%) of no electrolyte or a reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· SenTec AG

Recalled Item: SenTec Membrane Changer Set (1 charger plus 1 insert) - Recalled by SenTec...

The Issue: There is an increased chance (approx. 5%) of no electrolyte or a reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· Bard Peripheral Vascular Inc

Recalled Item: EnCor Breast Biopsy Probes Recalled by Bard Peripheral Vascular Inc Due to...

The Issue: There has been an increase in complaints related to leaks, suction issues,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· Bard Peripheral Vascular Inc

Recalled Item: EnCor Breast Biopsy Probes Recalled by Bard Peripheral Vascular Inc Due to...

The Issue: There has been an increase in complaints related to leaks, suction issues,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· Bard Peripheral Vascular Inc

Recalled Item: EnCor Breast Biopsy Probes Recalled by Bard Peripheral Vascular Inc Due to...

The Issue: There has been an increase in complaints related to leaks, suction issues,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· SenTec AG

Recalled Item: SenTec Membrane Changer Insert [5 pcs - Product Usage: is Recalled by SenTec...

The Issue: There is an increased chance (approx. 5%) of no electrolyte or a reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· Bard Peripheral Vascular Inc

Recalled Item: EnCor Breast Biopsy Probes Recalled by Bard Peripheral Vascular Inc Due to...

The Issue: There has been an increase in complaints related to leaks, suction issues,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· Rinovum Women's Health

Recalled Item: Revive Reusable Bladder Support Recalled by Rinovum Women's Health Due to...

The Issue: The product is unable to meet the use life of 31 cycles and may split or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2019· Oakworks Inc

Recalled Item: OAKWORKS Inc.Lithotripsy/Urology Table: CFLU401 Recalled by Oakworks Inc Due...

The Issue: Table assembly error with incorrect actuators for the lateral and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2019· Abbott Laboratories, Inc

Recalled Item: ARCHITECT C System Mixer - Product Usage: The ARCHITECT Clinical Recalled by...

The Issue: Mixer blade may separate from mixer due to the screw and nut failure and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2019· Medtronic Navigation, Inc.-Littleton

Recalled Item: Medtronic 0-arm TM 1000 Imaging Systems: Bl-700-00027-XXX and...

The Issue: The 0-arm 1000 Imaging System uses energy from the batteries to generate...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2019· Cardinal Health 200, LLC

Recalled Item: Monoject Standard Hypodermic Needle Recalled by Cardinal Health 200, LLC Due...

The Issue: Manufacturing defect was found for the cartridge component, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2019· Cardinal Health 200, LLC

Recalled Item: Monoject Standard Hypodermic Needle Recalled by Cardinal Health 200, LLC Due...

The Issue: Manufacturing defect was found for the cartridge component, which could...

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

Class II — Potential Health HazardOngoing