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. 2,701 recalls have been distributed to Wisconsin in the last 12 months.
Showing 6941–6960 of 28,744 recalls
Recalled Item: SenSight Connector Plug Recalled by Medtronic Neuromodulation Due to...
The Issue: Medtronic is requesting return of a small number of units of the SenSight...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SciCan STATIS SL S10001 Dental Handpieces-Intended for the removal of...
The Issue: Screw connection between the turbine head and the push button may loosen and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue G7m Anesthesia Gas Module Recalled by Philips North America Due...
The Issue: The 866173 lntelliVue G7m Anesthesia Gas Modules could have a component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Irvine Scientific Oil for Embryo Culture (Light Mineral Oil) # 9305 Recalled...
The Issue: Due to the detection of oil toxicity in several lots of Oil for Embryo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hologic 3Dimensions/Selenia Dimensions Models: RM-SDM-00001-3D SDM-00001-2D...
The Issue: C-Arm unexpected movement may cause blunt trauma should the tube arm impinge...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS Biograph mCT: a) Flow 64-4R Seismic Recalled by Siemens Medical...
The Issue: This is a potential problem with the locking mechanism that is used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS Biograph Vision: a) 450 Recalled by Siemens Medical Solutions USA,...
The Issue: This is a potential problem with the locking mechanism that is used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS Biograph Horizon 3R Mobile Recalled by Siemens Medical Solutions...
The Issue: This is a potential problem with the locking mechanism that is used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Folate 140 test kit- For in vitro diagnostic Recalled by Siemens...
The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Folate 700 test kit (REF)-For in vitro diagnostic Recalled by...
The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Folate 100 test kit-For in vitro diagnostic use Recalled by...
The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Folate 700 test kit- For in vitro diagnostic Recalled by Siemens...
The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Folate 500 test kit (REF)-For in vitro diagnostic Recalled by...
The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Folate 500 test kit- For in vitro diagnostic Recalled by...
The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: abm Respiratory Care Standart Breating Circuit with Face Mask - Recalled by...
The Issue: Incorrect expiration date on product label. The manufacturing date was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WishBone Medical Smart Correction Dual Joint Express Struts Recalled by...
The Issue: Firm identified that user may be unable to adjust the length of the Smart...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog Number / Product Description 0601600 2.7F Broviac CV Catheter...
The Issue: Due to the adhesive provided within the catheter repair kits maybe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Digital VIPR ROC-9839 Roberts Oxygen Ready to Use Digital VIPR Recalled by...
The Issue: Gauge malfunction: Digital gauge displays an incorrect tank pressure -...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Vanguard Knee System PS Open Box Femoral Recalled by Biomet, Inc. Due to...
The Issue: Components Incorrectly labeled as either smaller or larger and incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Vanguard Knee System PS Open Box Femoral Recalled by Biomet, Inc. Due to...
The Issue: Components Incorrectly labeled as either smaller or larger and incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.