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. 2,336 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,336 in last 12 months

Showing 2714127160 of 27,254 recalls

Medical DeviceJuly 27, 2010· Xoran Technologies, Inc.

Recalled Item: Xoran MiniCAT CT Scanner Recalled by Xoran Technologies, Inc. Due to A...

The Issue: A description of the defect in the product or the manner in which the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2010· Xoran Technologies, Inc.

Recalled Item: Xoran MiniCAT00202 Recalled by Xoran Technologies, Inc. Due to The MiniCAT...

The Issue: The MiniCAT CT Scanners subject to this notification failed to meet Xoran's...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2010· Xoran Technologies, Inc.

Recalled Item: Xoran Minicat00202 Recalled by Xoran Technologies, Inc. Due to The MiniCAT...

The Issue: The MiniCAT CT Scanners subject to this notification failed to meet Xoran's...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2010· Xoran Technologies, Inc.

Recalled Item: Xoran Minicat00158 Recalled by Xoran Technologies, Inc. Due to The MiniCAT...

The Issue: The MiniCAT CT Scanners subject to this notification failed to meet Xoran's...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2010· Kimberly-Clark Corporation

Recalled Item: Kimberly-Clark MIC Safety PEG Kit - Pull Type The Kimberly-Clark Recalled by...

The Issue: The placement guidewire diameter is too large and does not pass-through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2010· Kimberly-Clark Corporation

Recalled Item: Kimberly-Clark MIC PEG Kit - Pull Type The Kimberly-Clark MIC Recalled by...

The Issue: The placement guidewire diameter is too large and does not pass-through the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2010· Unimed Surgical Products, Inc.

Recalled Item: Product is labeled in part: "***MEDLINE***Extended PTFE Coated Blade with...

The Issue: On 6/16/2010 Unimed Surgical Products, Inc., 10401 Belcher Road, Largo, FL...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2010· Unimed Surgical Products, Inc.

Recalled Item: Product is labeled in part: "***MEDLINE***Standard PTFE Coated Needle 2.75"...

The Issue: On 6/16/2010 Unimed Surgical Products, Inc., 10401 Belcher Road, Largo, FL...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2010· Unimed Surgical Products, Inc.

Recalled Item: Product is labeled in part: "***MEDLINE***Extended PTFE Coated Needle 4.0"...

The Issue: On 6/16/2010 Unimed Surgical Products, Inc., 10401 Belcher Road, Largo, FL...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2010· Unimed Surgical Products, Inc.

Recalled Item: Product is labeled in part: "***MEDLINE***Extended PTFE Needle 6.5"...

The Issue: On 6/16/2010 Unimed Surgical Products, Inc., 10401 Belcher Road, Largo, FL...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2010· Unimed Surgical Products, Inc.

Recalled Item: Product is labeled in part: "***MEDLINE***Extended PTFE Coated Blade with...

The Issue: On 6/16/2010 Unimed Surgical Products, Inc., 10401 Belcher Road, Largo, FL...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2010· Unimed Surgical Products, Inc.

Recalled Item: Product is labeled in part: "***MEDLINE***Extended PTFE Coated Needle with...

The Issue: On 6/16/2010 Unimed Surgical Products, Inc., 10401 Belcher Road, Largo, FL...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2010· Unimed Surgical Products, Inc.

Recalled Item: Product is labeled in part: "***MEDLINE***Extended 5mm PTFE Coated Ball...

The Issue: On 6/16/2010 Unimed Surgical Products, Inc., 10401 Belcher Road, Largo, FL...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2010· Unimed Surgical Products, Inc.

Recalled Item: Product is labeled in part: "***MEDLINE***Extended PTFE Coated Blade 6.5...

The Issue: On 6/16/2010 Unimed Surgical Products, Inc., 10401 Belcher Road, Largo, FL...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2010· Unimed Surgical Products, Inc.

Recalled Item: Product is labeled in part: "***MEDLINE***Staight Microsurgical Needle 3cm...

The Issue: On 6/16/2010 Unimed Surgical Products, Inc., 10401 Belcher Road, Largo, FL...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2010· Unimed Surgical Products, Inc.

Recalled Item: Product is labeled in part: "***MEDLINE***Standard PTFE Coated Needle with...

The Issue: On 6/16/2010 Unimed Surgical Products, Inc., 10401 Belcher Road, Largo, FL...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2010· Unimed Surgical Products, Inc.

Recalled Item: Product is labeled in part: "***MEDLINE***Standard PTFE Coated Blade with...

The Issue: On 6/16/2010 Unimed Surgical Products, Inc., 10401 Belcher Road, Largo, FL...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2010· App Pharmaceuticals Llc

Recalled Item: HEPARIN LOCK FLUSH SOLUTION Recalled by App Pharmaceuticals Llc Due to CGMP...

The Issue: CGMP Deviations: Incomplete documentation associated with test results.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 20, 2010· App Pharmaceuticals Llc

Recalled Item: HEPARIN LOCK FLUSH SOLUTION Recalled by App Pharmaceuticals Llc Due to CGMP...

The Issue: CGMP Deviations: Incomplete documentation associated with test results.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2010· Cayenne Medical Inc.

Recalled Item: AperFix Femoral Implant Coring Removal Drill Recalled by Cayenne Medical...

The Issue: A review of product complaints in 2010 identified a trend for the Coring...

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

Class II — Potential Health HazardOngoing