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. 2,715 recalls have been distributed to Wisconsin in the last 12 months.
Showing 4561–4580 of 28,744 recalls
Recalled Item: BD Phoenix Yeast ID Panel is a self-inoculating (when used Recalled by...
The Issue: Esculin, a substrate used in other panels and normally in A16 well, was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix NMIC-306 Panel is a self-inoculating (when used with Recalled by...
The Issue: Products were found to have confirmed drug cross contamination prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...
The Issue: The potential for trocar seal disengagement when using mesh products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...
The Issue: The potential for trocar seal disengagement when using mesh products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...
The Issue: The potential for trocar seal disengagement when using mesh products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...
The Issue: The potential for trocar seal disengagement when using mesh products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...
The Issue: The potential for trocar seal disengagement when using mesh products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...
The Issue: The potential for trocar seal disengagement when using mesh products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Auto Suture" Structural Balloon Trocar Recalled by Covidien, LP Due...
The Issue: The potential for trocar seal disengagement when using mesh products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Patient Information Center iX (PIC iX) Recalled by Philips North America Due...
The Issue: It was found that the Care Assist mobile application (version 4.1.1 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareEvent Event Management System Recalled by Philips North America Due to...
The Issue: It was found that the Care Assist mobile application (version 4.1.1 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz SE & CO. KG Recalled by Karl Storz Endoscopy Due to Inadequate...
The Issue: Inadequate reprocessing validation evidence
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Performance Verifier I Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: The issue was mismatched diluent lots assembled into VITRO Chemistry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConvaTec CarboFlex Recalled by ConvaTec, Inc Due to The product does not...
The Issue: The product does not meet sterility assurance level.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O.T.D - Optimum Traction Device - Street Orange. Single use traction splint....
The Issue: Failure of adhesive to secure the pole insert.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz SE & CO. KG Recalled by Karl Storz Endoscopy Due to Inadequate...
The Issue: Inadequate reprocessing validation evidence
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz SE & CO. KG Recalled by Karl Storz Endoscopy Due to Inadequate...
The Issue: Inadequate reprocessing validation evidence
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Performance Verifier II Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: The issue was mismatched diluent lots assembled into VITRO Chemistry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII HEMI CLUSTER52E-Indicated for use in primary and revision patients...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII HEMI CLUSTER44B- Indicated for use in primary and revision...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.