Product Recalls in Wisconsin

Product recalls affecting Wisconsin — including food, drugs, consumer products, medical devices, and vehicles distributed to Wisconsin. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,515 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
2,515 in last 12 months

Showing 2616126180 of 28,744 recalls

Medical DeviceJune 27, 2013· Insight Instruments, Inc.

Recalled Item: MLS Torpedo Mini-Light Ophthalmic single-port illumination. Sutureless 25-...

The Issue: The product was registered and distributed as a Class I medical device and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2013· Siemens Healthcare Diagnostics

Recalled Item: ADVIA 120 Hematology Analyzer Recalled by Siemens Healthcare Diagnostics Due...

The Issue: The ADVIA 120 optics cover or hood is located on the very top of the ADVIA...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2013· Siemens Healthcare Diagnostics

Recalled Item: PSA Assays for use in the IMMULITE/IMMULITE 1000 Systems Analyzers Recalled...

The Issue: Customers complained of a positive bias in patient results on the IMMULITE/...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2013· Mar Cor Purification

Recalled Item: Mar Cor Purification Millenium HX Portable Reverse Osmosis System. Model...

The Issue: High inlet water pressure beyond specification and the solenoid valve does...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS zee and zeego x-ray Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Siemens issued a customer safety advisory notice and field safety corrective...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2013· Convatec Inc.

Recalled Item: ConvaTec Flexi-Seal SIGNAL + Recalled by Convatec Inc. Due to ConvaTec...

The Issue: ConvaTec notified their customers on 6/25/2013 regarding the manufacturing...

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

Class III — Low RiskOngoing
Medical DeviceJune 25, 2013· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur HCY Diluent - 10mL Bottle Catalog number 09877493 (124533)...

The Issue: ADVIA Centaur Homocysteine dilution recovery on the diluent identified the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2013· Convatec Inc.

Recalled Item: ConvaTec Flexi-Seal SIGNAL Fecal Management System Recalled by Convatec Inc....

The Issue: ConvaTec notified their customers on 6/25/2013 regarding the manufacturing...

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

Class III — Low RiskOngoing
Medical DeviceJune 24, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Sonopet Ultrasonic Aspirator Console 5450-852-000 (Console 230V) Product...

The Issue: A supplied component exhibiting corrosion was built into the power supply...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2013· Stelkast Co

Recalled Item: SC2316 Recalled by Stelkast Co Due to The firm became aware of an incident...

The Issue: The firm became aware of an incident relating to a breach of sterility in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Sonopet Ultrasonic Aspirator Console 5450-851-000(Console 100V) Product...

The Issue: A supplied component exhibiting corrosion was built into the power supply...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Sonopet Ultrasonic Aspirator Console (Console 110V with Pedal & Pole)...

The Issue: A supplied component exhibiting corrosion was built into the power supply...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Matrix 5.5.mm Left and Right Coronal Bender Product Usage: Recalled...

The Issue: A complaint was received of the tips of the Matrix 5.5.mm Left and Right...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo¿ Endovascular Occlusion Gel-2.5 mL LeGoo with 1 Cannula Pouch Recalled...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo¿ Endovascular Occlusion Gel-0.5 mL LeGoo w/ no Cannula Product...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo Internal Vessel Occluder .25mL Product Number: 10-0025 LeGoo is...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo Internal Vessel Occluder 2.5mL Product Number: 10-0250 LeGoo is...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo Internal Vessel Occluder 10mL Product Number: 10-1000 LeGoo is...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo¿ Endovascular Occlusion Gel-1.0 mL LeGoo with 3 Cannula Pouch Recalled...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2013· Genzyme Corporation, A Sanofi Company

Recalled Item: LeGoo Internal Vessel Occluder 5mL Product Number: 10-0500 LeGoo is Recalled...

The Issue: Product contains particulates (fibers)

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

Class II — Potential Health HazardOngoing