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. 2,313 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
2,313 in last 12 months

Showing 3244132460 of 47,027 recalls

Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Ray-Cot 3" x 3" : 60-15 Product Recalled by American...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Ray-Cot 1/2" x 1.5" : 60-08 Product Recalled by American...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Delicot non-xray 5 mm x 8 mm by American Surgical Company...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Ray-Cot 1/4" x 3" : 60-04 Product Recalled by American...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Ultracot 30 mm x 90 mm (Glassine) by American Surgical...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Americot White 1.5 cm x 5.5 cm by American Surgical...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· Shimadzu Medical Systems

Recalled Item: X-Ray Diagnostic Table Recalled by Shimadzu Medical Systems Due to Report of...

The Issue: Report of unintentional movement of table to reverse tilting.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Americot Blue 1/4" x 1/4" : 20-01S Recalled by American...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Cylindrical Sponges-Strung 1/2" x 1.5" : 70-02 Recalled by...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Ray-Cot 1/2" x 1" : 60-07 Product Recalled by American...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· Biocare Medical, LLC

Recalled Item: Mach 4 Mouse Probe vial within the Mach 4 Universal HRP-Polymer Kit Recalled...

The Issue: Biocare Medical has identified a single lot (082715) of its Mach 4 HRP...

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

Class III — Low RiskOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Delicot 9 mm x 50 mm : Recalled by American Surgical...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Delicot 15mm x 20mm Product Usage: Recalled by American...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Telfa 1/2" x 1/2" : 80-06 Product Recalled by American...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Ultracot 5 mm x 8 mm (Glassine) by American Surgical...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Delicot-J 15 mm x 20 mm : Recalled by American Surgical...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Uniqcot 1/2" x 1.5" : 67-08 Product Recalled by American...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Ray-Cot 1/2" x 2" : 60-29 Product Recalled by American...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
DrugMarch 31, 2016· Amerisource Health Services

Recalled Item: Fenofibrate Capsules (Micronized) Recalled by Amerisource Health Services...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date

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

Class III — Low RiskOngoing
Refund
DrugMarch 31, 2016· Invisiblu International LLC

Recalled Item: LGD-Xtreme (ligandrol LGD-4033) Recalled by Invisiblu International LLC Due...

The Issue: Marketed Without An Approved NDA/ANDA: Contains an unapproved drug,...

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

Class II — Potential Health HazardOngoing
Refund