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. 2,356 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,356 in last 12 months

Showing 1956119580 of 27,157 recalls

Medical DeviceFebruary 22, 2016· Pentax Medical Company

Recalled Item: Video Duodenoscope Recalled by Pentax Medical Company Due to Pentax Medical...

The Issue: Pentax Medical learned of reports of carbapenem-resistant Enterobacteriaceae...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2016· Innovative Ophthalmic Products, Inc

Recalled Item: Molteno3 Glaucoma Implants G-Series: GS-Single Plate 175mm2 (IOP reorder#:...

The Issue: Innovative Ophthalmic Products (IOP) is recalling the Molteno 3 G-Series...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego (system Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Possible leak in the cooling system, fluids could potentially seep into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2016· Horiba Instruments Inc

Recalled Item: ABX Pentra 400 (version 5.0.8 or lower) The ABX PENTRA Recalled by Horiba...

The Issue: Horiba Instruments, Inc. is recalling ABX Pentra 400( version 5.0.8 or...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Cios Alpha Recalled by Siemens Medical Solutions USA, Inc Due to Software...

The Issue: Software issues on Cios Alpha mobile C-Arm system

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2016· Integrated Science Systems Inc

Recalled Item: Sure Vue Color Staph 150T Recalled by Integrated Science Systems Inc Due to...

The Issue: Customer complaints of very weak reactions with the kit, or false negative...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2016· Horiba Instruments Inc

Recalled Item: Pentra C400 (version 1.1.2 or lower) The ABX PENTRA 400 Recalled by Horiba...

The Issue: Horiba Instruments, Inc. is recalling ABX Pentra 400( version 5.0.8 or...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Artis (system Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Possible leak in the cooling system, fluids could potentially seep into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Mckesson Medical Immaging

Recalled Item: McKesson Horizon Medical Imaging (HMI) products versions 4.6.1 to including...

The Issue: McKesson has identified a design deficiency where under rare circumstances,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Ortho-Clinical Diagnostics

Recalled Item: 1) VITROS¿ Immunodiagnostic Products Total Beta-hCG II Reagent Pack (Unique...

The Issue: When testing was conducted using certain lots, VITROS¿ Systems generated...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Artis zee/zeego Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Artis zee/zeego Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/zeego and Artis Q/Q.zen system Recalled by Siemens Medical...

The Issue: Due to a leak in the cooling system, fluids could potentially seep into the...

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

Class II — Potential Health HazardOngoing