Product Recalls in Idaho

Product recalls affecting Idaho — including food, drugs, consumer products, medical devices, and vehicles distributed to Idaho. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,395 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
2,395 in last 12 months

Showing 2772127740 of 27,833 recalls

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***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***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***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 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***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 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 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***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 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
Medical DeviceApril 26, 2010· GE OEC Medical Systems, Inc

Recalled Item: GE HC OEC 9900 Elite and GE OEC 9800 Fluoroscopes Recalled by GE OEC Medical...

The Issue: GE OEC recalled certain 9800 Fluoroscope & 9900 Elite Models because the...

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

Class II — Potential Health HazardOngoing