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. 2,322 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,322 in last 12 months

Showing 3122131240 of 47,027 recalls

Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Curved Spatula Electrode 28CM Item Code: E278128 The...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Wire L-Hook Electrode 28CM Item Code: E278328 The...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Nakanishi Inc.

Recalled Item: Diamond Coated Tips and Burs are accessories to the Ultrasonic Recalled by...

The Issue: Through an error, the labeling failed to include the symbol or other text...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Wire J-Hook Electrode Retractable 28CM Item Code:...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Wire J-Hook Electrode 36CM Item Code: E277336 The...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Curved Spatula Electrode 36CM Item Code: E277136 The...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Curved Spatula Electrode 45CM Item Code: E277145 The...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Flexible Laparoscopic Argon Electrodes Item Code:...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Wire L-Hook Electrode Retractable Item Code:...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Wire L-Hook Electrode Retractable Item Code:...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Flat L-Hook Electrode Retractable Item Code:...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Wire J-Hook Electrode 28CM Item Code: E278228 The...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Flat L-Hook Electrode 28cm Item Code: E278428 The...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Nakanishi Inc.

Recalled Item: Diamond Coated Tips and Burs are accessories to the air Recalled by...

The Issue: Through an error, the labeling failed to include the symbol or other text...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Wire J-Hook Electrode 45CM Item Code: E277345 The...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Wire J-Hook Electrode 36CM Item Code: E277236 The...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Medtronic

Recalled Item: Valleylab Laparoscopic Flexible Laparoscopic Argon Electrodes 3" Item Code:...

The Issue: Potential for compromise of the package resulting in a breach of the sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2016· Philips Electronics North America Corporation

Recalled Item: UNIQ 1.0: UNIQ FD10 Recalled by Philips Electronics North America...

The Issue: Increase in the failure rate of certain low-voltage DC power supplies (DCPS)

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2016· Philips Electronics North America Corporation

Recalled Item: Allura Xper with release R8.2: Allura Xper FD10 Recalled by Philips...

The Issue: Increase in the failure rate of certain low-voltage DC power supplies (DCPS)

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 7, 2016· TZ Medical, Inc.

Recalled Item: Neptune Plus (Hemostatic Pad) Recalled by TZ Medical, Inc. Due to Neptune...

The Issue: Neptune Plus was mis-labeled and included the statement WITH ANTIMICROBIAL...

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

Class II — Potential Health HazardOngoing