Product Recalls in Ohio
Product recalls affecting Ohio — including food, drugs, consumer products, medical devices, and vehicles distributed to Ohio. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,955 recalls have been distributed to Ohio in the last 12 months.
Showing 20401–20420 of 30,087 recalls
Recalled Item: 2.5 mm TI Calibrated Reaming Rod 850 mm 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: TBS iNsight Version v.3.0.1 Product Usage: TBS iNsight is a Recalled by...
The Issue: The FRAX adjusted for TBS values are not correct when: The FRAX feature is...
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: 8500M Handheld Pulse Oximeter Recalled by Nonin Medical, Inc Due to Nonin...
The Issue: Nonin manufactures and sells two 8500 handheld pulse oximeters (Model 8500...
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: 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: 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: 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: 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 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: 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: 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: sigma spectrum VOLUMETRIC INFUSION PUMP with Master Drug Library Recalled by...
The Issue: A correction was issued for the SIGMA Spectrum Infusion Pump with Master...
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: 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: 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) 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.