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. 2,348 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,348 in last 12 months

Showing 2162121640 of 27,157 recalls

Medical DeviceMarch 9, 2015· Specialty Appliance Works, Inc.

Recalled Item: TS Crown Component 4UR (5/pk) Recalled by Specialty Appliance Works, Inc....

The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Specialty Appliance Works, Inc.

Recalled Item: Upper Right Telescope Unibodies (5/pk) and Upper Left Telescope Unibodies...

The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Specialty Appliance Works, Inc.

Recalled Item: Herbst Universal Nut which is used in a Herbst Appliance Recalled by...

The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Specialty Appliance Works, Inc.

Recalled Item: LR Telescoping Cantilever Arms (5/pk) and LL Telescoping Cantilever Arms...

The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Specialty Appliance Works, Inc.

Recalled Item: TS ROC Crown Component 4UR (5/pk) Recalled by Specialty Appliance Works,...

The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Specialty Appliance Works, Inc.

Recalled Item: Specialty MiniScope Mech. Set Size 18 Recalled by Specialty Appliance Works,...

The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Specialty Appliance Works, Inc.

Recalled Item: TS Herbst Nuts with Backing (10/pk) and TS Herbst Nuts Recalled by Specialty...

The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Specialty Appliance Works, Inc.

Recalled Item: HTM Mechanism Set Set 16 Recalled by Specialty Appliance Works, Inc. Due to...

The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Specialty Appliance Works, Inc.

Recalled Item: MiniScope Hst ROC Crown 15 Patient Kit Recalled by Specialty Appliance...

The Issue: The Universal Nut, a component of the orthodontic Herbst Appliance was made...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujifilm Endoscope Models ED-250XL5 ED-250XT5 ED-450XT5 ED-450XL5 Product...

The Issue: Fujifilm is conducting a corrective action due to an FDA inspection.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujifilm Endoscope Model ED-530XT Product Usage: This product is a Recalled...

The Issue: Fujifilm is reporting a corrective action due to an FDA inspection.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: CardioMD III (Uninterruptible Power Supply (UPS) accessory devices) Computed...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity TF (Uninterruptible Power Supply (UPS) accessory devices) Computed...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: iCT SP (Uninterruptible Power Supply (UPS) accessory devices) Computed...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: GEMINI TF PET/CT 64 Slice (Uninterruptible Power Supply (UPS) accessory...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Precedence 6 (Uninterruptible Power Supply (UPS) accessory devices) Computed...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance CT 16 Slice Air (Uninterruptible Power Supply (UPS) accessory...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: MX 16 Slice Phase II (Uninterruptible Power Supply (UPS) accessory Recalled...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: MX 16 Slice (Uninterruptible Power Supply (UPS) accessory devices) Computed...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Wright Medical Technology, Inc.

Recalled Item: CROSSCHECK(R) Plating system Recalled by Wright Medical Technology, Inc. Due...

The Issue: The minor diameter, major diameter, thread pitch, and pitch on the...

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

Class II — Potential Health HazardOngoing