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. 2,558 recalls have been distributed to Wisconsin in the last 12 months.
Showing 19501–19520 of 28,744 recalls
Recalled Item: 3.0 mm Guide Rod/950 mm with Smooth Tip Recalled by Synthes (USA) Products...
The Issue: The peel pouches for the affected reaming rods and extraction hooks are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.0 mm Reaming Rod/950 mm Recalled by Synthes (USA) Products LLC Due to The...
The Issue: The peel pouches for the affected reaming rods and extraction hooks are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4205 Journey Rolling Walker Product Usage: used to assist people in walking...
The Issue: Nova Medical is recalling the Journey Rolling Walker because the screws used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lumex Recalled by GF Health Products, Inc Due to GF Health Products, Inc.,...
The Issue: GF Health Products, Inc., in conjunction with OKIN America, has initiated a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PET Infusion Pump Recalled by Bayer Healthcare Due to The Source...
The Issue: The Source Administration Sets (SAS) used with the Medrad Intego PET...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexLab Automation Modules Recalled by Siemens Healthcare Diagnostics, Inc....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Devon Light Glove sub-assembly non-sterile For Kit Packers Product...
The Issue: Added Instructions for Use: After application, inspect the Light Glove for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ORCHESTRA PLUS Programmer A portable device Recalled by Sorin Group USA,...
The Issue: Sorin Group USA, Inc. announces a voluntary field action for the ORCHESTRA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Devon Light Glove packaged in sterile surgical kits : Recalled by...
The Issue: Added Instructions for Use: After application, inspect the Light Glove for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aptio Automation Modules Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Possible overheating of power cord plugs used to connect to FlexLab and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ORCHESTRA Programmer A portable device Recalled by Sorin Group USA, Inc....
The Issue: Sorin Group USA, Inc. announces a voluntary field action for the ORCHESTRA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Restoris RIO Reamer Handle Recalled by Mako Surgical Corporation Due...
The Issue: Failure of the Offset Cup Reamer Handle not engaging its mating components.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System The Monaco system is used to make Recalled by Elekta, Inc....
The Issue: When creating 3D plans using either MU or Dose weighting modes, if the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thayer MiniSpacer Dual Spray MDI Adapter Counter Incrementing Actuator with...
The Issue: The insert and case label description of the device incorrectly reads...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Professional Hospital Supply Recalled by Covidien LLC Due to Added...
The Issue: Added Instructions for Use: After application, inspect the Light Glove for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5...
The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Gender Solutions" Patellofemoral Joint Prosthesis Milling Handpiece...
The Issue: Complaints have been reported that the handpiece is inoperable. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4...
The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4...
The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5...
The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.