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. 2,128 recalls have been distributed to Ohio in the last 12 months.
Showing 5701–5720 of 30,087 recalls
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps Recalled by Stryker Corporation...
The Issue: An error was identified on the expiration date of the product label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Universal Viewer Workflow Manager Recalled by GE Healthcare Due...
The Issue: When using Universal Viewer or Centricity Universal Viewer with Workflow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: F2-01 Frame Recalled by GE Medical Systems China Co., Ltd. Due to There is a...
The Issue: There is a potential interruption of data communication between E-modules...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Viewer Workflow Manager Recalled by GE Healthcare Due to When...
The Issue: When using Universal Viewer or Centricity Universal Viewer with Workflow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Real Intelligence CORI RI.KNEE v2.0 TKA (Total Knee Arthroplasty) software...
The Issue: CORI software was missing a planning stage that appears in cases of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AU/DxC AU Chemistry Transferrin Immune complexes formed in Recalled by...
The Issue: The firm has identified that the Transferrin reagent does not meet the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Meera Mobile Operating Table-to support and position the patient immediately...
The Issue: Under certain conditions, an issue might prevent the device from performing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venue Go Standard Carts Ref: (H45181VC and H45103VCW) Recalled by GE MEDICAL...
The Issue: Some Venue Go Standard Carts can develop an internal failure of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T HD SYS. CDX BLUESTAR Recalled by Fresenius Medical Care Holdings, Inc....
The Issue: Potential PCBA leaching from tubing of hemodialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis CII Safe ES Recalled by CareFusion 303, Inc. Due to When global...
The Issue: When global edit is used to update multiple formulary properties...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T Hemodialysis System without CDX Recalled by Fresenius Medical Care...
The Issue: Potential PCBA leaching from tubing of hemodialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T HD SYS. CDX W/BIBAG BLUESTAR Recalled by Fresenius Medical Care...
The Issue: Potential PCBA leaching from tubing of hemodialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T GEN 2 Bibag without CDX Recalled by Fresenius Medical Care Holdings,...
The Issue: Potential PCBA leaching from tubing of hemodialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T Hemodialysis System w/Bibag Recalled by Fresenius Medical Care...
The Issue: Potential PCBA leaching from tubing of hemodialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T HD SYS. W/O CDX W/BIBAG BLUESTAR Recalled by Fresenius Medical Care...
The Issue: Potential PCBA leaching from tubing of hemodialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T Hemodialysis SYS Recalled by Fresenius Medical Care Holdings, Inc. Due...
The Issue: Potential PCBA leaching from tubing of hemodialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.