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. 2,279 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,279 in last 12 months

Showing 3908139100 of 47,027 recalls

Medical DeviceAugust 27, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: The Ysio Systems with software version VC10 The Ysio enables Recalled by...

The Issue: Siemens discovered that an unlikely error may occur on the Ysio system with...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2014· Spacelabs Healthcare Inc

Recalled Item: Spacelabs Medical Patient Monitor is a Physiological Recalled by Spacelabs...

The Issue: The clinician did not realize the monitor was in END CASE mode and was...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2014· Bio-Detek, Inc.

Recalled Item: ZOLL Pro-padz Sterile Adult Multi-Function Electrodes with 10-ft (3 m)...

The Issue: Sterility of device is not assured

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2014· Bio-Detek, Inc.

Recalled Item: ZOLL Pro-padz Sterile Adult Multi-Function Electrodes Part number: 8900-4012...

The Issue: Sterility of device is not assured

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2014· Bard Peripheral Vascular Inc

Recalled Item: Bard DuaLok Breast Lesion Localization Wire Recalled by Bard Peripheral...

The Issue: Bard Peripheral is recalling the Bard DuaLok Breast Lesion Localization Wire...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2014· Bio-Detek, Inc.

Recalled Item: ZOLL Pro-padz Sterile Adult Multi-Function Electrodes ((singles) Part...

The Issue: Sterility of device is not assured

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

Class II — Potential Health HazardOngoing
DrugAugust 25, 2014· Actavis Inc

Recalled Item: Vancomycin Hydrochloride Capsule Recalled by Actavis Inc Due to Subpotent Drug

The Issue: Subpotent Drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 25, 2014· Actavis Inc

Recalled Item: Vancomycin Hydrochloride Capsule Recalled by Actavis Inc Due to Subpotent Drug

The Issue: Subpotent Drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodAugust 25, 2014· Hi-Tech Pharmacal Co., Inc.

Recalled Item: Rx CHOICE brand LIQUID VITAMIN C Recalled by Hi-Tech Pharmacal Co., Inc. Due...

The Issue: The firm is recalling Rx CHOICE brand LIQUID VITAMIN C because the active...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 25, 2014· Navilyst Medical, Inc

Recalled Item: PICC Convenience Kit with Accessories Recalled by Navilyst Medical, Inc Due...

The Issue: NMI was notified by the manufacturer of the 10 ml BD PosiFlush SF Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2014· Navilyst Medical, Inc

Recalled Item: PICC Convenience Kit with Accessories Recalled by Navilyst Medical, Inc Due...

The Issue: NMI was notified by the manufacturer of the 10 ml BD PosiFlush SF Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2014· Navilyst Medical, Inc

Recalled Item: BioFlo PICC with ENDEXO Technology Maximal Barrier Nursing Kit Recalled by...

The Issue: NMI was notified by the manufacturer of the 10 ml BD PosiFlush SF Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2014· Navilyst Medical, Inc

Recalled Item: PICC Convenience Kit with Accessories Recalled by Navilyst Medical, Inc Due...

The Issue: NMI was notified by the manufacturer of the 10 ml BD PosiFlush SF Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2014· Navilyst Medical, Inc

Recalled Item: BioFlo PICC with ENDEXO Technology and PASV Valve Technology Maximal...

The Issue: NMI was notified by the manufacturer of the 10 ml BD PosiFlush SF Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2014· Navilyst Medical, Inc

Recalled Item: PICC Convenience Kit with Accessories Recalled by Navilyst Medical, Inc Due...

The Issue: NMI was notified by the manufacturer of the 10 ml BD PosiFlush SF Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2014· Navilyst Medical, Inc

Recalled Item: PICC Convenience Kit with Accessories Recalled by Navilyst Medical, Inc Due...

The Issue: NMI was notified by the manufacturer of the 10 ml BD PosiFlush SF Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2014· Navilyst Medical, Inc

Recalled Item: BioFlo PICC with ENDEXO Technology Maximal Barrier Nursing Kit Recalled by...

The Issue: NMI was notified by the manufacturer of the 10 ml BD PosiFlush SF Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2014· Navilyst Medical, Inc

Recalled Item: PICC Convenience Kit with Accessories Recalled by Navilyst Medical, Inc Due...

The Issue: NMI was notified by the manufacturer of the 10 ml BD PosiFlush SF Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2014· Navilyst Medical, Inc

Recalled Item: PICC Convenience Kit with Accessories Recalled by Navilyst Medical, Inc Due...

The Issue: NMI was notified by the manufacturer of the 10 ml BD PosiFlush SF Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2014· Navilyst Medical, Inc

Recalled Item: PICC Convenience Kit with Accessories Recalled by Navilyst Medical, Inc Due...

The Issue: NMI was notified by the manufacturer of the 10 ml BD PosiFlush SF Saline...

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

Class II — Potential Health HazardOngoing