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. 2,790 recalls have been distributed to Ohio in the last 12 months.
Showing 3561–3580 of 30,087 recalls
Recalled Item: ClotTriever XL Catheter Recalled by Inari Medical - Oak Canyon Due to...
The Issue: Thrombectomy system catheter instructions for use updated to reduce adverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: prodisc C SK Recalled by Centinel Spine, Inc. Due to During the assembly of...
The Issue: During the assembly of Prodisc C, a blue discoloration was observed on a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: prodisc C SK Recalled by Centinel Spine, Inc. Due to During the assembly of...
The Issue: During the assembly of Prodisc C, a blue discoloration was observed on a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BACTEC MGIT 960 PZA Kit)- IVD qualitative procedure for Recalled by...
The Issue: May intermittently produce falsely resistant results for pyrazinamide (PZA)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mazor X. Model Number Recalled by Mazor Robotics Ltd Due to Software...
The Issue: Software anomalies which can result in two separate issues: A lagging screen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PE Centrifuge Temperature Controlled Recalled by Beckman Coulter Biomedical...
The Issue: The adhesive joint between the plastic socket and metal component of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power Express Recalled by Beckman Coulter Biomedical GmbH Due to The...
The Issue: The adhesive joint between the plastic socket and metal component of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PE Centrifuge Recalled by Beckman Coulter Biomedical GmbH Due to The...
The Issue: The adhesive joint between the plastic socket and metal component of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectrum Wireless Battery Modules A/B/G/N Recalled by Baxter Healthcare...
The Issue: The Spectrum WBM may fail to auto-document infusion status information back...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Spectrum Wireless Battery Modules A/B/G/N Recalled by Baxter...
The Issue: The Spectrum WBM may fail to auto-document infusion status information back...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WAVEWRITER ALPHA: Model: SC-1216 Recalled by Boston Scientific...
The Issue: Spinal Cord Stimulation (SCS) Implantable Pulse Generator (IPG) may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo Recalled by Philips Respironics, Inc. Due to Firm has released a...
The Issue: Firm has released a mandatory software update Version 1.05.10.00 and a User...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo Universal Ventilator Recalled by Philips Respironics, Inc. Due...
The Issue: Firm has released a mandatory software update Version 1.05.10.00 and a User...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo EV300 -- Model Number/ Model Description: BL2200X15B Trilogy Evo...
The Issue: Firm has released a mandatory software update Version 1.05.10.00 and a User...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TiBrid Stand Alone Intervertebral Body Fusion Device Recalled by Omnia...
The Issue: Failure of fusion system instruments in the field.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TiBrid Stand Alone Intervertebral Body Fusion Device Recalled by Omnia...
The Issue: Failure of fusion system instruments in the field.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Desc: Product Name: CLEARCUT SB INTREPID 2.2 ANG Model/Catalog...
The Issue: Alcon has detected an increase in complaint reports related to sharpness for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: TOTAL PLUS Recalled by Alcon Research LLC Due to Alcon has...
The Issue: Alcon has detected an increase in complaint reports related to sharpness for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Desc: Product Name: CLEARCUT SLIT FULL HANDLE2.6MM ANG DUAL Recalled...
The Issue: Alcon has detected an increase in complaint reports related to sharpness for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Desc: Product Name: CLEARCUT SLIT FULL HANDLE2.75MM ANG DUA Recalled...
The Issue: Alcon has detected an increase in complaint reports related to sharpness for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.