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. 2,541 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,541 in last 12 months

Showing 18611880 of 27,157 recalls

Medical DeviceMarch 19, 2025· Siemens Healthcare Diagnostics Inc

Recalled Item: epoc BGEM BUN Test Card (25 pk) for the epoc Blood Analysis System Recalled...

The Issue: The occurrence of discrepant high pH results in samples introduced with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: It was identified that the Medline Sterile Water and Medline Sterile 0.9%...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: It was identified that the Medline Sterile Water and Medline Sterile 0.9%...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: It was identified that the Medline Sterile Water and Medline Sterile 0.9%...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: It was identified that the Medline Sterile Water and Medline Sterile 0.9%...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: It was identified that the Medline Sterile Water and Medline Sterile 0.9%...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2025· Siemens Healthcare Diagnostics Inc

Recalled Item: epoc BGEM Crea Test Card (25 pk) for the epoc Blood Analysis System Recalled...

The Issue: The occurrence of discrepant high pH results in samples introduced with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2025· Avanos Medical, Inc.

Recalled Item: Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog...

The Issue: Lack of sterility assurance for closed suction catheter systems

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 19, 2025· Avanos Medical, Inc.

Recalled Item: Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog...

The Issue: Lack of sterility assurance for closed suction catheter systems

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 19, 2025· Avanos Medical, Inc.

Recalled Item: Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog...

The Issue: Lack of sterility assurance for closed suction catheter systems

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 19, 2025· Avanos Medical, Inc.

Recalled Item: Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog...

The Issue: Lack of sterility assurance for closed suction catheter systems

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 19, 2025· Avanos Medical, Inc.

Recalled Item: Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog...

The Issue: Lack of sterility assurance for closed suction catheter systems

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 19, 2025· Avanos Medical, Inc.

Recalled Item: Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog...

The Issue: Lack of sterility assurance for closed suction catheter systems

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 19, 2025· Avanos Medical, Inc.

Recalled Item: Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog...

The Issue: Lack of sterility assurance for closed suction catheter systems

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 19, 2025· Avanos Medical, Inc.

Recalled Item: Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog...

The Issue: Lack of sterility assurance for closed suction catheter systems

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 18, 2025· Smith & Nephew, Inc.

Recalled Item: META-TAN LAG/COMPRESSION SCREW KIT 90MM/85MM Recalled by Smith & Nephew,...

The Issue: Integrated Lag/Compression Screw Kit has a compression screw with hexagon...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2025· Abbott Laboratories

Recalled Item: Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number:...

The Issue: When expired reagents are scanned or manually entered, the system will...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2025· Abbott Laboratories

Recalled Item: Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number:...

The Issue: When expired reagents are scanned or manually entered, the system will...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2025· Abbott Laboratories

Recalled Item: Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number:...

The Issue: When expired reagents are scanned or manually entered, the system will...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2025· Abbott Laboratories

Recalled Item: Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number:...

The Issue: When expired reagents are scanned or manually entered, the system will...

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

Class II — Potential Health HazardOngoing