Product Recalls in Vermont

Product recalls affecting Vermont — including food, drugs, consumer products, medical devices, and vehicles distributed to Vermont. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,243 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,243 in last 12 months

Showing 4690146920 of 47,027 recalls

Medical DeviceJuly 27, 2010· Xoran Technologies, Inc.

Recalled Item: Xoran Mini 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 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***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 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 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***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***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 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 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 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 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 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
Medical DeviceApril 5, 2010· Philips Healthcare Inc.

Recalled Item: Philips Healthcare Computed Tomography X-Ray System. These devices are...

The Issue: Philips Healthcare discovered the customer was performing CTDI measurements...

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

Class II — Potential Health HazardOngoing
DrugMarch 1, 2010· K C Pharmaceuticals Inc

Recalled Item: Eye Drops advanced relief (Dextran 70 0.1% Recalled by K C Pharmaceuticals...

The Issue: Labeling: Label Mix-Up: Incorrect back labeling of the immediate container...

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

Class II — Potential Health HazardOngoing
Refund