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. 1,786 recalls have been distributed to Wisconsin in the last 12 months.
Showing 43401–43420 of 52,482 recalls
Recalled Item: Amerigel Post-Op Surgical Kits . Kit includes: Amerigel Wound Dressing...
The Issue: Not approved labeling claims (antimicrobial and autolytic debridement)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibila Insert UC Recalled by Ortho Development Corporation Due to Ortho...
The Issue: Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PS Tibial Insert Recalled by Ortho Development Corporation Due to Ortho...
The Issue: Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibila Insert CK Recalled by Ortho Development Corporation Due to Ortho...
The Issue: Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pivot Bipolar Cup 22x42/43-51/53mm Recalled by Ortho Development Corporation...
The Issue: Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Patella 38mm Recalled by Ortho Development Corporation Due to Ortho...
The Issue: Ortho Development is recalling various Pivot Bipolar Cup, Patella, PS Tibial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Ascenda Intrathecal Catheter models 8780 and 8781 Recalled by...
The Issue: Medtronic is removing specific lots of the Ascenda Intrathecal Catheters and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlowCOUPLER. An implantable device that is used to detect blood Recalled by...
The Issue: Baxter Healthcare is recalling the FlowCOUPLER Device because there is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LACTATED RINGER'S and 5% DEXTROSE Injection USP Recalled by Hospira Inc. Due...
The Issue: Non-Sterility: Confirmed customer complaint of particulate matter floating...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medical Positioning Rapid Response HUT table Recalled by Medical Positioning...
The Issue: Excessive weight on the table will cause tables with the affected component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Positioning Rapid Response HUT table Recalled by Medical Positioning...
The Issue: Excessive weight on the table will cause tables with the affected component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Positioning Rapid Response HUT table with Dual 2 Way Drop Section...
The Issue: Excessive weight on the table will cause tables with the affected component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Positioning Rapid Response HUT table Recalled by Medical Positioning...
The Issue: Excessive weight on the table will cause tables with the affected component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Foley Urinary Catheter Insertion Tray with 10cc syringe Recalled by...
The Issue: Labeling error: The manufacturing date is the same as the expiration date....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clonidine Base Micronized Recalled by Gyma Laboratories Of Amer,Inc Due to...
The Issue: cGMP Deviations: GYMA laboratories Inc. has recalled multiple Active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Propranolol HCl Recalled by Gyma Laboratories Of Amer,Inc Due to cGMP...
The Issue: cGMP Deviations: GYMA laboratories Inc. has recalled multiple Active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dipyridamole API Recalled by Gyma Laboratories Of Amer,Inc Due to cGMP...
The Issue: cGMP Deviations: GYMA laboratories Inc. has recalled multiple Active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clonidine HCL Recalled by Gyma Laboratories Of Amer,Inc Due to cGMP...
The Issue: cGMP Deviations: GYMA laboratories Inc. has recalled multiple Active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The Hulka Clip is a sterile packaged medical device that Recalled by Richard...
The Issue: Richard Wolf Medical Instrument Corporation is recalling Hulka Clip Tubal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene BC-GN Test Kit (Catalog number 20-005-021) includes: 1) 20 Recalled...
The Issue: Nanosphere Inc. has recently determined through four customer complaints...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.