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. 2,543 recalls have been distributed to Wisconsin in the last 12 months.

52,482 total recalls
2,543 in last 12 months

Showing 2178121800 of 28,744 recalls

Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: The Drug Detection Agency 6 Panel Cup Body and Lid w/Adult (AU) Recalled by...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: DrugSmart 10 Test Cup (PCP & MDMA) Recalled by Ameditech Inc Due to...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: THERMO FISHER 6 DRUG CASSETTE Recalled by Ameditech Inc Due to Ameditech is...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: ArcPoint Labs 10 Panel Dip Screen (OXY) Recalled by Ameditech Inc Due to...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: iCup Drug Screen Cup Recalled by Ameditech Inc Due to Ameditech is recalling...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: DrugSmart 11 Test Cup Recalled by Ameditech Inc Due to Ameditech is...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: 11 Panel Cup (OPI2000) w/Adult Recalled by Ameditech Inc Due to Ameditech is...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: 11 Panel Dip Card (OPI 2000) Recalled by Ameditech Inc Due to Ameditech is...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: 1 Step 12 Panel Cup Recalled by Ameditech Inc Due to Ameditech is recalling...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: DrugCheck Pipette 10 Drug Test Recalled by Ameditech Inc Due to Ameditech is...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 20, 2015· Ameditech Inc

Recalled Item: EDI BZO UNCUT SHEET-CARD Recalled by Ameditech Inc Due to Ameditech is...

The Issue: Ameditech is recalling drug abuse tests because they have shown reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2015· Bard Peripheral Vascular Inc

Recalled Item: FLAIR Endovascular Stent Graft Recalled by Bard Peripheral Vascular Inc Due...

The Issue: Bard Peripheral Vascular (BPV) is recalling the Bard Flair Endovascular...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2015· Synthes (USA) Products LLC

Recalled Item: Synthes Application Instrument for Sternal ZIPFIX. Indications for use...

The Issue: Certain lots of the Application Instrument for Sternal ZIPFIX that were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2015· Invivo Corporation

Recalled Item: The system provides the ability to transmit patient data files for storage...

The Issue: Display of SpO2 and Non-Invasive Blood Pressure (NIBP) Measurements May Freeze

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2015· Elekta, Inc.

Recalled Item: Monaco - Radiation Treatment Planning used to make treatment plans Recalled...

The Issue: Unintended update of Dose and MU and Incorrect Assignment of Bolus.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2015· Utah Medical Products, Inc

Recalled Item: Myelo-Nate CSF Sampling Kit Recalled by Utah Medical Products, Inc Due to...

The Issue: Utah Medical is conducting a recall of Myelo-Nate CSF Sampling Kit due to an...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2015· Euro Diagnostica AB

Recalled Item: DIASTAT anti-Nuclear antibody (ANA) / DIASTAT ANA ELISA. Catalog Number:...

The Issue: Complaint investigation concluded that although product quality requirements...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2015· Covidien LLC

Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip Recalled by...

The Issue: Incorrectly packaged with a 90 degree bend at the distal tip

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2015· Covidien LLC

Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip Recalled by...

The Issue: Incorrectly packaged with a 90 degree bend at the distal tip

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2015· Covidien LLC

Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip Recalled by...

The Issue: Incorrectly packaged with a 90 degree bend at the distal tip

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

Class II — Potential Health HazardOngoing