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. 1,984 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
1,984 in last 12 months

Showing 21212140 of 27,157 recalls

Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: C-SECTION PPS Recalled by American Contract Systems Inc Due to ACS is unable...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: LAPAROSCOPY PACK Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: EAR PACK Recalled by American Contract Systems Inc Due to ACS is unable to...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: LAPAROSCOPY PACK Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· Integra LifeSciences Corp.

Recalled Item: AURORA Surgiscope System Recalled by Integra LifeSciences Corp. Due to...

The Issue: Possibility for the obturator to break (separate).

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: LACERATION TRAY Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: DELIVERY PACK Recalled by American Contract Systems Inc Due to ACS is unable...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: CYSTO Recalled by American Contract Systems Inc Due to ACS is unable to...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: LAPAROSCOPY PACK Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: LACERATION TRAY Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: HIP SCOPE Recalled by American Contract Systems Inc Due to ACS is unable to...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: OPEN HEART ADULT - SIDE A Recalled by American Contract Systems Inc Due to...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: LABOR & DELIVERY PACK Recalled by American Contract Systems Inc Due to ACS...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: C-SECTION PACK Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: GENERAL LAPAROSCOPIC PACK-LF Recalled by American Contract Systems Inc Due...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: DIAGNOSTIC NEURO IR TRAY Recalled by American Contract Systems Inc Due to...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: CENTRAL LINE PICC Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: MAJOR VASCULAR PACK Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline ReNewal Reprocessed Livewire Steerable Electrophysiology Catheters...

The Issue: Devices may have higher than expected amounts of bacterial endotoxin.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2025· American Contract Systems Inc

Recalled Item: GENERAL ANGIO PACK Recalled by American Contract Systems Inc Due to ACS is...

The Issue: ACS is unable to confirm product sterilization assurance requirements were...

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

Class II — Potential Health HazardOngoing