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 4694146960 of 47,027 recalls

Medical DeviceJuly 13, 2009· Toshiba American Medical Systems Inc

Recalled Item: Whole Body X--ray Scanner This device is indicated as a Recalled by Toshiba...

The Issue: 1. It has been found that in raw data processing for Go&Return helical...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2009· GE OEC Medical Systems, Inc

Recalled Item: OEC IT3000 Recalled by GE OEC Medical Systems, Inc Due to GE Healthcare...

The Issue: GE Healthcare Surgery had discovered that using the Inverted Headset...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2009· Karl Storz Endoscopy America Inc

Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...

The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2009· Karl Storz Endoscopy America Inc

Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...

The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2009· Karl Storz Endoscopy America Inc

Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...

The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2009· Karl Storz Endoscopy America Inc

Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...

The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2009· Karl Storz Endoscopy America Inc

Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...

The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2009· Karl Storz Endoscopy America Inc

Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...

The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2009· Karl Storz Endoscopy America Inc

Recalled Item: Loop Recalled by Karl Storz Endoscopy America Inc Due to Possible damage to...

The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2009· Karl Storz Endoscopy America Inc

Recalled Item: Knife Recalled by Karl Storz Endoscopy America Inc Due to Possible damage to...

The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2009· Karl Storz Endoscopy America Inc

Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...

The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2009· Karl Storz Endoscopy America Inc

Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...

The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2009· Karl Storz Endoscopy America Inc

Recalled Item: Loop Recalled by Karl Storz Endoscopy America Inc Due to Possible damage to...

The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2009· Karl Storz Endoscopy America Inc

Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...

The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2009· Alere San Diego, Inc.

Recalled Item: Triage TOX Drug Screen Panel Recalled by Alere San Diego, Inc. Due to...

The Issue: Biosite is recalling the Triage TOX Drug Screen kits where the box...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2009· Sunquest Information Systems, Inc.

Recalled Item: Sunquest Encompass The reporting site is using the Encompass software...

The Issue: Sunquest is recalling the Sunquest Encompass versions 2.4 and later because...

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

Class III — Low RiskOngoing
FoodApril 7, 2009· Trophy Nut Co Inc

Recalled Item: America's Choice 9 oz. Giant Pistachios Recalled by Trophy Nut Co Inc Due to...

The Issue: The product is being recalled because it was manufactured using pistachios...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodApril 7, 2009· Trophy Nut Co Inc

Recalled Item: Trophy Nut Brand 1.5 oz. Red Pistachio Tube and Nut Recalled by Trophy Nut...

The Issue: The product is being recalled because it was manufactured using pistachios...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodApril 7, 2009· Trophy Nut Co Inc

Recalled Item: Trophy Nut Brand 1.5 oz. tube Recalled by Trophy Nut Co Inc Due to Potential...

The Issue: The product is being recalled because it was manufactured using pistachios...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodApril 7, 2009· Trophy Nut Co Inc

Recalled Item: Trophy Nut Brand 6 oz. natural pistachios Recalled by Trophy Nut Co Inc Due...

The Issue: The product is being recalled because it was manufactured using pistachios...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund