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. 2,557 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
2,557 in last 12 months

Showing 1998120000 of 28,744 recalls

Medical DeviceJuly 11, 2016· Clark Laboratories, Inc. (dba,Trinity Biotech USA)

Recalled Item: Trinity Biotech Captia Measles IgM Recalled by Clark Laboratories, Inc....

The Issue: The product lot failed to meet QC acceptance criteria during stability...

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

Class III — Low RiskOngoing
Medical DeviceJuly 11, 2016· B. Braun Medical, Inc.

Recalled Item: Affected Pain Control Tray Component (5% Lidocaine Hydrochloride and 7.5%...

The Issue: B. Braun Medical Inc. is voluntarily recalling specific lots of their Custom...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio2 PT/INR Professional Monitoring System Model Number: 55128A...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio Replacement Monitor Model Number: 0100137 Usage: The INRatio...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: INRatio Prothrombin Time (PT) Monitoring System Model Number: 0100007...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio PT/INR System Professional Model Numbers: 0100004 Product...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio2 PT/INR Professional Testing System Model Number: 0200431...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· American National Mfg Inc

Recalled Item: Panacea Air Pro Mattress Control Unit Recalled by American National Mfg Inc...

The Issue: The Panacea Air Pro Mattress Control Unit is being recalled due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2016· C.R. Bard, Inc.

Recalled Item: Option-vm Urinary Catheter. Male use only. Latex Free. Sterile Recalled by...

The Issue: During an FDA inspection it was found out that the Practical Foley Catheters...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2016· C.R. Bard, Inc.

Recalled Item: Option-vf Urinary Catheter. Female use only. Latex Free. Sterile Recalled by...

The Issue: During an FDA inspection it was found out that the Practical Foley Catheters...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio2 Replacement Monitor (Home) Model Number: 0200457 Product...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio2 PT/INR Home Monitoring System Model Number: 0200432 Recalled...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio PT/INR Test Strips Model Number: 0100071 Recalled by Alere San...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2016· Alere San Diego, Inc.

Recalled Item: Alere INRatio/ INRatio2 PT/INR Test Strips Model Number: 99007EU Recalled by...

The Issue: Alere San Diego is initiating a voluntary recall for the Alere...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 10, 2016· Trumpf Medical Systems, Inc.

Recalled Item: Operating Table TruSystem 7000 U Recalled by Trumpf Medical Systems, Inc....

The Issue: Three complaints describing TruSystem tables unexpectedly descending...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2016· Trumpf Medical Systems, Inc.

Recalled Item: Floor Mounting Column TS 7500 U Recalled by Trumpf Medical Systems, Inc. Due...

The Issue: Three complaints describing TruSystem tables unexpectedly descending...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2016· Trumpf Medical Systems, Inc.

Recalled Item: Mobile Column TruSystem 7500 Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Three complaints describing TruSystem tables unexpectedly descending...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2016· Trumpf Medical Systems, Inc.

Recalled Item: Stationary Column TruSystem 7599 Recalled by Trumpf Medical Systems, Inc....

The Issue: Three complaints describing TruSystem tables unexpectedly descending...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· Nakanishi Inc.

Recalled Item: Diamond Coated Tips and Burs are accessories to the air Recalled by...

The Issue: Through an error, the labeling failed to include the symbol or other text...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2016· BioMerieux SA

Recalled Item: NucliSENS easyMAG Magnetic Silica The NucliSENS easyMAG accessory products...

The Issue: Several customer complaints about amplification performance issues when...

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

Class I — Serious Health HazardOngoing