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. 2,736 recalls have been distributed to Wisconsin in the last 12 months.
Showing 1761–1780 of 28,744 recalls
Recalled Item: Brand Name: Catalyst+ Product Name: C4D software used in conjunction...
The Issue: Software issue with scanning equipment that can results in the filed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endopath Echelon Vascular White Reload for Advanced Placement Tip (35mm...
The Issue: Firm has received an increase in reports regarding inadvertent instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Precision Sampling Set Recalled by Capnia Inc Due to Sampling set nasal...
The Issue: Sampling set nasal cannula used with End-Tidal Carbon Monoxide (ETCO)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOWER EXTREMITY Recalled by American Contract Systems, Inc. Due to Test...
The Issue: Test results for cast padding component included in procedure trays shows...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Cathena Safety IV Catheter BD Multiguard Technology 18 GA x 1.25 IN...
The Issue: Due to a manufacturing defect IV catheter may have a hole in the septum,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Single Intragastric Linton Balloon Tube Recalled by C.R. Bard Inc Due...
The Issue: Due to customer complaints, there is a potential for users to be unable to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Check=Flo Performer Introducer Recalled by Cook Incorporated Due to Cook...
The Issue: Cook Medical identified that devices from the affected device lots may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Check=Flo Performer Introducer Recalled by Cook Incorporated Due to Cook...
The Issue: Cook Medical identified that devices from the affected device lots may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Blakemore Esophageal-Nasogastric Tube (Intermediate) Recalled by C.R....
The Issue: Due to customer complaints, there is a potential for users to be unable to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ Blakemore Esophageal-Nasogastric Tube (Child) Recalled by C.R. Bard...
The Issue: Due to customer complaints, there is a potential for users to be unable to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Minnesota Four Lumen Esophagogastric Tamponade Tube Recalled by C.R....
The Issue: Due to customer complaints, there is a potential for users to be unable to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Blakemore Esophageal-Nasogastric Tube (Adult) Recalled by C.R. Bard Inc...
The Issue: Due to customer complaints, there is a potential for users to be unable to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WB XL Anatomic Healing Abutment XC. Endosseous Dental Implant Abutments....
The Issue: Incorrect blister labelling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIGENE Gram Negative Blood Culture (BC-GN) Nucleic Acid Test Recalled by...
The Issue: It was determined that the consumable issue may result in No Call - INT CTL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tempus Pro Patient Monitor Recalled by Remote Diagnostic Technologies Ltd....
The Issue: software issue that causes an error screen on a portable vital signs monitor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Homocysteine Calibrator (2 Pack). Siemens Material Number:...
The Issue: Certain lots of Atellica IM Homocysteine Calibrator and ADVIA Centaur HCY...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur HCY Calibrator (2 Pack). Siemens Material Number: 10310376....
The Issue: Certain lots of Atellica IM Homocysteine Calibrator and ADVIA Centaur HCY...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Tempus Pro Patient Monitor Recalled by Remote Diagnostic...
The Issue: Patient Monitor software update to address issues:1)May freeze at startup...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glidewell HT Implant Twist Drill ¿1.5 x 8 mm " Recalled by Prismatik...
The Issue: Due to packaging mix up. Package of finished devices were reported to have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products CRP Slides. One sales unit contains 5 cartridges...
The Issue: Product was incorrectly assigned GEN 88 instead of GEN 83 on product carton,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.