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. 2,521 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,521 in last 12 months

Showing 52015220 of 47,027 recalls

Medical DeviceJune 3, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: 190904 2008K@HOME HEMODIALYSIS SYSTEM W/ BIBAG - Blood Pump Rotor spare part...

The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: 190395: 2008K@HOME MACHINE Recalled by Fresenius Medical Care Holdings, Inc....

The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2024· Stryker Corporation

Recalled Item: The Non-Sterile Flyte hood covers the user s head and Recalled by Stryker...

The Issue: Expired Products distributed to customers

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2024· Qiagen Sciences LLC

Recalled Item: QIAcube Connect MDx - IVD Instrument designed to perform automated Recalled...

The Issue: Heater shaker module does not perform heating if the temperature is set...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: 190828: 2008K@HOME HEMODIALYSIS SYSTEM - Blood Pump Rotor spare part...

The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2024· Nalu Medical, Inc.

Recalled Item: Neurostimulation Kit (Ported Recalled by Nalu Medical, Inc. Due to...

The Issue: Neurostimulation Systems have a manufacturing non-conformance that may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2024· Treace Medical Concepts, Inc.

Recalled Item: Nanoplasty 3D Bunion Correction System Implant Recalled by Treace Medical...

The Issue: Potential issue causing a higher frequency of interference with locking...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM MULTIX MT - Intended Radiographic X ray Table is Recalled by Siemens...

The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Stryker Sustainability Solutions

Recalled Item: Recalled by Stryker Sustainability Solutions Due to Mislabeling

The Issue: Mislabeling; tourniquet cuff packaging labeled as dual port single bladder...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Avanos Medical, Inc.

Recalled Item: MIC-KEY* Gastric-Jejunal Feeding Tube Kit Recalled by Avanos Medical, Inc....

The Issue: The IFU was missing some risk information requested by another country to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Vertix Solitaire - The Vertix MD Trauma has been Recalled by Siemens...

The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Maquet Cardiovascular, LLC

Recalled Item: The VASOVIEW HEMOPRO 2 Endoscopic Vessel Harvesting System is designed...

The Issue: There were 27 complaints between March 22, 2024, and April 30, 2024, related...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM MULTIX MP - Intended Radiographic X ray Table is Recalled by Siemens...

The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Olympus Corporation of the Americas

Recalled Item: Soltive Pro SuperPulsed Laser System Recalled by Olympus Corporation of the...

The Issue: Difficulties in pairing the wireless footswitch with the Soltive Laser,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: MULTIX TOP - Intended Use: The Multix TOP I PRO Recalled by Siemens Medical...

The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: ZE for Vertix Solitaire - The AXIOM Vertix Solitaire is Recalled by Siemens...

The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM MULTIX MP - Inended Radiographic X ray Table is Recalled by Siemens...

The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM MULTIX MT - Intended Radiographic X ray Table is Recalled by Siemens...

The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Maquet Cardiovascular, LLC

Recalled Item: The VASOVIEW HEMOPRO Endoscopic Vessel Harvesting Systems is designed for...

The Issue: There were 27 complaints between March 22, 2024, and April 30, 2024, related...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Olympus Corporation of the Americas

Recalled Item: Soltive Premium SuperPulsed Laser System Recalled by Olympus Corporation of...

The Issue: Difficulties in pairing the wireless footswitch with the Soltive Laser,...

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

Class II — Potential Health HazardOngoing