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. 2,440 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,440 in last 12 months

Showing 1498115000 of 27,254 recalls

Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: CLAMP STYLE CATH. CONNECTOR 18-19 GA- LF Recalled by B. Braun Medical, Inc....

The Issue: The catheter connectors may not stay closed during in and in some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2018· B. Braun Medical, Inc.

Recalled Item: CE17TOD CONT EPIDURAL TRAY LF Recalled by B. Braun Medical, Inc. Due to The...

The Issue: The catheter connectors may not stay closed during in and in some cases,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2018· Beaver Visitec

Recalled Item: Beaver Accu-Temp High Temperature Cautery Recalled by Beaver Visitec Due to...

The Issue: A small number of devices in this lot may have a melted cap and a hole...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2018· Abbott Laboratories, Inc

Recalled Item: Abbott ARCHITECT Creatine Kinase Recalled by Abbott Laboratories, Inc Due to...

The Issue: The product has a stability issue which may lead to an error code indicating...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2018· Abbott Laboratories, Inc

Recalled Item: Abbott ARCHITECT Creatine Kinase Recalled by Abbott Laboratories, Inc Due to...

The Issue: The product has a stability issue which may lead to an error code indicating...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Alcon Research Laboratories Ltd.

Recalled Item: Alcon or Endure Ophthalmic Microscope Product Usage: Used for low Recalled...

The Issue: Potential for the optical head to detach from the stand due to the lack of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Abbott Laboratories, Inc

Recalled Item: Abbott ARCHITECT c16000 Processing Module Recalled by Abbott Laboratories,...

The Issue: There is a potential to generate incorrect results on the instrument if...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Abbott Laboratories, Inc

Recalled Item: Abbott ARCHITECT c8000 Processing Module Recalled by Abbott Laboratories,...

The Issue: There is a potential to generate incorrect results on the instrument if...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2018· Abbott Laboratories, Inc

Recalled Item: Abbott ARCHITECT c4000 Processing Module Recalled by Abbott Laboratories,...

The Issue: There is a potential to generate incorrect results on the instrument if...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper F020 DR Table Recalled by Philips Electronics North America...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: AlluraXperFOlO/lO Recalled by Philips Electronics North America Corporation...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: INTEGRIS Allura 9 Recalled by Philips Electronics North America Corporation...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: INTEGRIS CV Recalled by Philips Electronics North America Corporation Due to...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: INTEGRIS Allura 15-12 (biplane) Recalled by Philips Electronics North...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: Cesar-DMCP-Visub(HM2000/3000) Recalled by Philips Electronics North America...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· In2bones USA, LLC

Recalled Item: CoLink(TM) Lapidus Plate XP Recalled by In2bones USA, LLC Due to CoLink(TM)...

The Issue: CoLink(TM) Lapidus Plate +2mm Right and Left, were laser marked incorrectly....

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD1O C Recalled by Philips Electronics North America Corporation...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: NTEGRIS Allura 9 0 FDXD Recalled by Philips Electronics North America...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: INTEGRIS Allura 9 F FDXD Recalled by Philips Electronics North America...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2018· Philips Electronics North America Corporation

Recalled Item: AIIuraXperFDlO/10 Recalled by Philips Electronics North America Corporation...

The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...

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

Class II — Potential Health HazardOngoing