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. 2,257 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,257 in last 12 months

Showing 4090140920 of 47,027 recalls

Medical DeviceDecember 24, 2013· ICU Medical, Inc.

Recalled Item: 5" (13 cm) Appx 0.23 ml Recalled by ICU Medical, Inc. Due to ICU Medical is...

The Issue: ICU Medical is recalling certain lots of the NanoClave Needlefree Connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2013· ICU Medical, Inc.

Recalled Item: 6.5" (16.5 cm) Appx 0.30 ml Recalled by ICU Medical, Inc. Due to ICU Medical...

The Issue: ICU Medical is recalling certain lots of the NanoClave Needlefree Connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2013· ICU Medical, Inc.

Recalled Item: 13" Smallbore Ext Set w/4 Gang 4-Way Stopcock w/Baseplate Recalled by ICU...

The Issue: ICU Medical is recalling certain lots of the NanoClave Needlefree Connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2013· ICU Medical, Inc.

Recalled Item: 7" (18 cm) Appx 0.26 ml Recalled by ICU Medical, Inc. Due to ICU Medical is...

The Issue: ICU Medical is recalling certain lots of the NanoClave Needlefree Connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2013· ICU Medical, Inc.

Recalled Item: 87" (221 cm) Appx 2.9 ml Recalled by ICU Medical, Inc. Due to ICU Medical is...

The Issue: ICU Medical is recalling certain lots of the NanoClave Needlefree Connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2013· ICU Medical, Inc.

Recalled Item: 7" (18 cm) Appx 0.31 ml Recalled by ICU Medical, Inc. Due to ICU Medical is...

The Issue: ICU Medical is recalling certain lots of the NanoClave Needlefree Connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2013· ICU Medical, Inc.

Recalled Item: 8" (20 cm) Appx 0.51 ml Recalled by ICU Medical, Inc. Due to ICU Medical is...

The Issue: ICU Medical is recalling certain lots of the NanoClave Needlefree Connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 24, 2013· ICU Medical, Inc.

Recalled Item: 10" (25 cm) Appx 0.38 ml Recalled by ICU Medical, Inc. Due to ICU Medical is...

The Issue: ICU Medical is recalling certain lots of the NanoClave Needlefree Connector...

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

Class II — Potential Health HazardOngoing
DrugDecember 23, 2013· Hospira Inc.

Recalled Item: Lidocaine HCl Injection Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter- Confimed customer complaint of particulates...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 23, 2013· Watson Laboratories Inc

Recalled Item: Carisoprodol Tablets Recalled by Watson Laboratories Inc Due to Presence of...

The Issue: Presence of Foreign Substance; metal particulates were visually observed in...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 23, 2013· Mckesson Information Solutions LLC

Recalled Item: Horizon Medical Imaging Recalled by Mckesson Information Solutions LLC Due...

The Issue: Images may be archived to an incorrect or invalid archive location resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2013· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON SC2000 Power Input: 100-240VAC Recalled by Siemens Medical Solutions...

The Issue: The locking mechanism that is intended to hold the control panel in a fixed...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2013· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON SC2000 Ultrasound System Recalled by Siemens Medical Solutions USA,...

The Issue: The user interface assembly on the ACUSON SC2000 may become loose with the...

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

Class II — Potential Health HazardOngoing
DrugDecember 20, 2013· Carefusion 2200 Inc

Recalled Item: CareFusion Scrub Care Surgical Scrub Brush-Sponge/Nail Cleaner With 15%...

The Issue: Subpotent Drug: CareFusion is recalling the CareFusion Scrub Care Surgical...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2013· Carefusion 2200 Inc

Recalled Item: CareFusion Scrub Care Surgical Scrub Brush-Sponge/Nail Cleaner With 9%...

The Issue: Subpotent Drug: CareFusion is recalling the CareFusion Scrub Care Surgical...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 20, 2013· Watson Laboratories, Inc.-(Actavis) - Florida

Recalled Item: Diclofenac Sodium and Misoprostol Delayed-Release Tablets Recalled by Watson...

The Issue: Failed Tablet/Capsule Specifications: Split tablets were found in the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 20, 2013· Siemens Healthcare Diagnostics

Recalled Item: IMMULITE/IMMULITE 1000 Systems Androstenedione (Test Code AND) Recalled by...

The Issue: Siemens Healthcare Diagnostics confirmed over-recovery of samples with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2013· Siemens Healthcare Diagnostics

Recalled Item: IMMULITE 2000/2000 XPi Systems Androstenedione (Test Code AND) Recalled by...

The Issue: Siemens Healthcare Diagnostics confirmed over-recovery of samples with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2013· Perrigo Diabetes Care

Recalled Item: Orbit soft Infusion sets Recalled by Perrigo Diabetes Care Due to Perrigo...

The Issue: Perrigo was notified by our supplier, Ypsomed AG, that they are recalling...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2013· GE Healthcare, LLC

Recalled Item: CARESCAPE Monitor B850 Recalled by GE Healthcare, LLC Due to There is a...

The Issue: There is a potential for communication loss associated with the F5-01 Frame...

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

Class II — Potential Health HazardOngoing