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 52215240 of 27,157 recalls

Medical DeviceNovember 6, 2023· Nurse Assist, LLC

Recalled Item: Sterile Water: Product Name/Product Code: USP STERILE WATER SYRINGE/1030A...

The Issue: Sodium chloride irrigation USP, and sterile water for irrigation USP, that...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 6, 2023· Nurse Assist, LLC

Recalled Item: 0.9% Sodium Chloride: Brand Name: Product Name/Product Code: MAC MEDICAL:...

The Issue: Sodium chloride irrigation USP, and sterile water for irrigation USP, that...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 3, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: STERILE BETADINE Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to The...

The Issue: The product description on the labeling includes the word "Sterile" or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2023· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Allura systems with monoplane fixed ceiling mounts: 722001 Allura...

The Issue: Ceiling mounted L-arm contains a rotation cover that may potentially be...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2023· Liberty Medical Solutions, LLC

Recalled Item: Multi-Mode Stimulator Recalled by Liberty Medical Solutions, LLC Due to The...

The Issue: The instruction manuals that were included with the Multi-Mode Stimulators...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: STERILE STERILE PREP STICK Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: The product description on the labeling includes the word "Sterile" or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: STERILE PVP Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to The...

The Issue: The product description on the labeling includes the word "Sterile" or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: STERILE POVIDONE Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to The...

The Issue: The product description on the labeling includes the word "Sterile" or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: PVP SOLUTION SING STRL Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: The product description on the labeling includes the word "Sterile" or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2023· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Azurion systems with monoplane fixed ceiling mounts: 722078 Azurion...

The Issue: Ceiling mounted L-arm contains a rotation cover that may potentially be...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2023· Inpeco S.A.

Recalled Item: Roche Cobas 8000 and Cobas PRO Interface Module (CO8 IM)- Recalled by Inpeco...

The Issue: Firmware of the Interface Module with Roche Cobas 8000 and Cobas PRO (CO8...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: STERILE PVP SLN KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: The product description on the labeling includes the word "Sterile" or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: STERILE PVP SOLUTION Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: The product description on the labeling includes the word "Sterile" or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: CENTRAL LINE BLOOD CULTURE DRA Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: This recall is being issued due to items within the kit have expired prior...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2023· B. Braun Medical, Inc.

Recalled Item: Infusomat Administration Sets as listed below: 362031 Infusomat Space Pump...

The Issue: In affected products, the tubing outer diameter may vary in size or the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 1, 2023· Atrium Medical Corporation

Recalled Item: Atrium Oasis Drain Single W / AC Recalled by Atrium Medical Corporation Due...

The Issue: A sterilization nonconformance prematurely aged the product by 48.3 days,...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: BLOOD CULTURE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: This recall is being issued due to items within the kit have expired prior...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: 24 BLOOD CULTURE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: This recall is being issued due to items within the kit have expired prior...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2023· CHANGE HEALTHCARE CANADA COMPANY

Recalled Item: Change Healthcare Stratus Imaging PACS 1.4 and Stratus Imaging Share 1.4...

The Issue: Under certain circumstances, information from HL7 messages received by...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: PERIPHERAL BLOOD CULTURE DRAW Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: This recall is being issued due to items within the kit have expired prior...

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

Class II — Potential Health HazardOngoing