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. 2,503 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,503 in last 12 months

Showing 73417360 of 27,157 recalls

Medical DeviceOctober 24, 2022· Whele LLC DBA Perch

Recalled Item: Mighty Bliss Electric Heating Pad Recalled by Whele LLC DBA Perch Due to The...

The Issue: The products may have the potential to burn customers. Firm has received...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 24, 2022· Whele LLC DBA Perch

Recalled Item: Mighty Bliss Electric Heating Pad Recalled by Whele LLC DBA Perch Due to The...

The Issue: The products may have the potential to burn customers. Firm has received...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 24, 2022· Tollos

Recalled Item: Infection Control (IC) Lifting Strap used with the following Cirrus Recalled...

The Issue: Two customers reported four incidents in which the lifting strap broke while...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2022· Philips North America Llc

Recalled Item: Philips ProxiDiagnost N90 1.0 (Model 706100) and ProxiDiagnost N90 1.1...

The Issue: Potential table stop due to a broken tabletop cable: On the ProxiDiagnost...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2022· Intersect ENT, Inc.

Recalled Item: Propel Mini Mometasone Furoate Sinus Implant Recalled by Intersect ENT, Inc....

The Issue: Sinus Implant product label displays incorrect product information...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2022· Howmedica Osteonics Corp.

Recalled Item: Simplex HV With Gentamicin CE Recalled by Howmedica Osteonics Corp. Due to...

The Issue: Simplex HV With Gentamicin CE, 10 PACKS (P/N 6193-1-010) were distributed to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2022· CoreLink LLC

Recalled Item: CoreLink LLC Recalled by CoreLink LLC Due to Specific lots of FLXfit...

The Issue: Specific lots of FLXfit implants have internal components that may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2022· Remel Inc

Recalled Item: Thermo SCIENTIFIC Recalled by Remel Inc Due to An internal technical...

The Issue: An internal technical investigation has confirmed that Thermo Scientific"...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 20, 2022· Remel Inc

Recalled Item: Thermo SCIENTIFIC Recalled by Remel Inc Due to An internal technical...

The Issue: An internal technical investigation has confirmed that Thermo Scientific"...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 20, 2022· Remel Inc

Recalled Item: Thermo SCIENTIFIC Recalled by Remel Inc Due to An internal technical...

The Issue: An internal technical investigation has confirmed that Thermo Scientific"...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 20, 2022· Remel Inc

Recalled Item: Thermo SCIENTIFIC Recalled by Remel Inc Due to An internal technical...

The Issue: An internal technical investigation has confirmed that Thermo Scientific"...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 20, 2022· Remel Inc

Recalled Item: Thermo SCIENTIFIC Recalled by Remel Inc Due to An internal technical...

The Issue: An internal technical investigation has confirmed that Thermo Scientific"...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 20, 2022· Remel Inc

Recalled Item: Thermo SCIENTIFIC Recalled by Remel Inc Due to An internal technical...

The Issue: An internal technical investigation has confirmed that Thermo Scientific"...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 20, 2022· Remel Inc

Recalled Item: Thermo SCIENTIFIC Recalled by Remel Inc Due to An internal technical...

The Issue: An internal technical investigation has confirmed that Thermo Scientific"...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 20, 2022· Remel Inc

Recalled Item: Thermo SCIENTIFIC Recalled by Remel Inc Due to An internal technical...

The Issue: An internal technical investigation has confirmed that Thermo Scientific"...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 20, 2022· Remel Inc

Recalled Item: Thermo SCIENTIFIC Sensititre Plate Recalled by Remel Inc Due to An internal...

The Issue: An internal technical investigation has confirmed that Thermo Scientific"...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 20, 2022· CooperSurgical, Inc.

Recalled Item: NEO-fit Neonatal Endotracheal Tube Grip Recalled by CooperSurgical, Inc. Due...

The Issue: Firm has received 11 complaints involving a loose or detached metal clips,...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2022· Atrium Medical Corporation

Recalled Item: Atrium Ocean Wet Suction Water Seal Chest Drain- Product Code: 2002-000...

The Issue: Warehouse experienced temperature excursions in July and August 2021. It was...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2022· Baxter Healthcare Corporation

Recalled Item: Hill-Rom Progressa Bed System Recalled by Baxter Healthcare Corporation Due...

The Issue: The compression links on impacted Progressa beds, listed in Appendix A, may...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2022· Visionsense, Ltd.

Recalled Item: VS3 Iridium - Visionsense Infrared (IR) Fluorescence Miniature Microscope...

The Issue: XXX

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

Class II — Potential Health HazardOngoing