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. 892 recalls have been distributed to Vermont in the last 12 months.

47,027 total recalls
892 in last 12 months

Showing 44601–44620 of 47,027 recalls

Medical DeviceDecember 20, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension(R) IRON Calibrator (DC85) Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics has received complaints of IRON calibrations...

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

Class III — Low RiskOngoing
Medical DeviceDecember 20, 2012· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 6 Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: Philips Healthcare received reports from the field stating the patient table...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2012· Medisystems a NX Stage Company

Recalled Item: Medisystems 15 Gauge x 3/5 inch Buttonhole Needle Set Product Recalled by...

The Issue: A total of 5 (ea) single needle pouches are mislabeled as 15 Ga x1" instead...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Total Iron Binding Capacity (IBCT) Flex Reagent Cartridge. An...

The Issue: The analytical sensitivity claim of 6 ug/dL (1.1 umol/L) in the Instructions...

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

Class III — Low RiskOngoing
Medical DeviceDecember 19, 2012· Hamilton Medical Inc

Recalled Item: HAMILTON-T1 Ventilator with software versions 1.1.2 or lower. The HAMILTON...

The Issue: Analysis of a customer complaint has shown that during ventilation of small...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2012· Elekta, Inc.

Recalled Item: Elekta Synergy XVI. Radiation Therapy Digital Imager. Product XVI R3.5.1...

The Issue: The DICOM tags do not contain sufficient information for XVI to identify the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista (R) Urinary/Cerebrospinal Fluid Protein (UCFP) Flex (R)...

The Issue: Siemens has confirmed an increase on absorbance errors when calibrating...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Leica Microsystems (Schweiz) Ag

Recalled Item: Surgical microscope The device is used to improve the visibility Recalled by...

The Issue: The brake in the Z axis and/or brakes in the AB and C axes failed during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Leica Microsystems (Schweiz) Ag

Recalled Item: Surgical microscope The device is used to improve the visibility Recalled by...

The Issue: The brake in the Z axis and/or brakes in the AB and C axes failed during...

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

Class II — Potential Health HazardOngoing
DrugDecember 18, 2012· Watson Pharmaceuticals

Recalled Item: Taztia XT(diltiazem HCI extended release capsules Recalled by Watson...

The Issue: Failed Dissolution Specification: Out of a specification result occurred...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 18, 2012· Belmora LLC

Recalled Item: Flanax (aluminum hydroxide Recalled by Belmora LLC Due to Defective...

The Issue: Defective Container: Product lacks tamper evident breakaway band on cap.

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

Class III — Low RiskOngoing
Refund
DrugDecember 18, 2012· Matrixx Initiatives Inc

Recalled Item: Zicam Extreme Congestion Relief (oxymetazoline HCl) nasal gel Recalled by...

The Issue: Microbial Contamination of Non-Sterile Products: Product may be contaminated...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 18, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Medical Surgical Bed Recalled by Stryker Medical Division of Stryker...

The Issue: Stryker Medical Model 3002S3EX and Model 3005S3EX beds built between March...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Cardinal Health

Recalled Item: Needle Counters with Blade Disarmer Recalled by Cardinal Health Due to Small...

The Issue: Small holes (approximately 1 mm or less) found in device unit level...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Cardinal Health

Recalled Item: Needle Counters with Blade Disarmer Recalled by Cardinal Health Due to Small...

The Issue: Small holes (approximately 1 mm or less) found in device unit level...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Cardinal Health

Recalled Item: Needle Counters with Blade Disarmer Recalled by Cardinal Health Due to Small...

The Issue: Small holes (approximately 1 mm or less) found in device unit level...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Cardinal Health

Recalled Item: Needle Counters with Blade Disarmer Recalled by Cardinal Health Due to Small...

The Issue: Small holes (approximately 1 mm or less) found in device unit level...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Cardinal Health

Recalled Item: Needle Counters with Blade Disarmer Recalled by Cardinal Health Due to Small...

The Issue: Small holes (approximately 1 mm or less) found in device unit level...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Cardinal Health

Recalled Item: Needle Counters Recalled by Cardinal Health Due to Small holes...

The Issue: Small holes (approximately 1 mm or less) found in device unit level...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2012· Cardinal Health

Recalled Item: Needle Counters Recalled by Cardinal Health Due to Small holes...

The Issue: Small holes (approximately 1 mm or less) found in device unit level...

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

Class II — Potential Health HazardOngoing