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.
Showing 2601–2620 of 27,157 recalls
Recalled Item: dS Breast 16ch 3.0T Recalled by Philips North America Llc Due to Potential...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST SENSE Breast Coil Recalled by Philips North America Llc Due to Potential...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mammotrak Interventional Coil 1.5T Recalled by Philips North America Llc Due...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mammotrak Diagnostic Coil 3.0T Recalled by Philips North America Llc Due to...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva TX Interventional Coil 3.0T Recalled by Philips North America Llc...
The Issue: Potential safety issue where a patient may be harmed while preparing for or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FACSLyric 2L4C Instrument US Recalled by Becton, Dickinson and Company, BD...
The Issue: On October 18, 2024, BD has identified through customer complaints and an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FACSLyric 3L12C Instrument RUO Recalled by Becton, Dickinson and Company, BD...
The Issue: On October 18, 2024, BD has identified through customer complaints and an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FACSLyric 3L10C Instrument US-IVD Recalled by Becton, Dickinson and Company,...
The Issue: On October 18, 2024, BD has identified through customer complaints and an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FACSLyric 3L8C Instrument US-IVD Recalled by Becton, Dickinson and Company,...
The Issue: On October 18, 2024, BD has identified through customer complaints and an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Device Description: FACSLyric 2L6C Instrument US Recalled by Becton,...
The Issue: On October 18, 2024, BD has identified through customer complaints and an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exacta External Drainage and Monitoring System: 27581 KIT 27581 EXACTA...
The Issue: Due to complaints received reporting cracks and/or leaks of the stopcocks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Becker External Drainage and Monitoring System: 24146 EDMS 24146 BECKER...
The Issue: Due to complaints received reporting cracks and/or leaks of the stopcocks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health SMS Elastic Cuff Thumbhook Level 3 Isolation Gown Recalled...
The Issue: Isolation Gowns were manufactured with raw materials that may fail the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convertor Isolation Gown Recalled by Cardinal Health 200, LLC Due to...
The Issue: Isolation Gowns were manufactured with raw materials that may fail the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arial Server Software Versions 11.1.4 through 11.1.6 Recalled by Securitas...
The Issue: Certain software versions will not notify end users of calls initiated by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD COR GX Instrument Version or Model: 443990 Catalog Number: 443990...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Synapsys Informatics Solution (Laboratory Solution) Version or Model:...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BACTEC FX Recalled by Becton Dickinson & Co. Due to BD confirmed that...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD MAX System Recalled by Becton Dickinson & Co. Due to BD confirmed that...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cartiva Synthetic Cartilage Implant (SCI) Catalog: CAR-06-US (6mm) Recalled...
The Issue: Patients implanted with synthetic cartilage implant, may experience a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.