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. 2,727 recalls have been distributed to Ohio in the last 12 months.
Showing 13041–13060 of 30,087 recalls
Recalled Item: OARtrac PLUS CLINICAL DETECTOR UNIT Catalog Number: OTS-V2-Plus - Product...
The Issue: May result in readings outside of the expected accuracy range.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICRO-PSD HDR Recalled by Angiodynamics, Inc. Due to May result in readings...
The Issue: May result in readings outside of the expected accuracy range.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICRO-PSD Electron Recalled by Angiodynamics, Inc. Due to May result in...
The Issue: May result in readings outside of the expected accuracy range.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICRO-PSD EXTERNAL BEAM PHOTON Recalled by Angiodynamics, Inc. Due to May...
The Issue: May result in readings outside of the expected accuracy range.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation stand-alone software treatment planning system Recalled by...
The Issue: Editing a static arc beam may unexpectedly set the MU of the beam to its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA SYSTEM CONROL N + P (ref. 00678) Recalled by Diagnostica Stago, Inc. Due...
The Issue: A positive bias was confirmed to exists on the STA - Unicalibrator levels...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA UNICALIBRATOR (ref. 00675) Recalled by Diagnostica Stago, Inc. Due to A...
The Issue: A positive bias was confirmed to exists on the STA - Unicalibrator levels...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elasto-Gel Absorbent Wound Dressing Recalled by Southwest Technologies Inc...
The Issue: Elasto-Gel Wound Dressing may be contaminated with mold.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BOND Polymer Detection Kit Recalled by Leica Microsystems, Inc. Due to BOND...
The Issue: BOND Polymer Detection kits (DS9800) were held out of storage longer than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Habib EUS RFA Recalled by Boston Scientific Corporation Due to During...
The Issue: During testing on the Habib EUS RFA device, a temperature increase was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Habib EUS RFA Recalled by Boston Scientific Corporation Due to During...
The Issue: During testing on the Habib EUS RFA device, a temperature increase was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revaclear Capillary Dialyzer 300 Recalled by Baxter Healthcare Corporation...
The Issue: There is the potential presence of particular matter in the header caps of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PneumoDart Recalled by Tytek Medical Inc Due to A defect involving an...
The Issue: A defect involving an occluded needle was discovered during a training exercise.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm" O2 Imaging System Recalled by Medtronic Navigation, Inc.-Littleton...
The Issue: Due to a manufacturing issue affecting particular O-arm" O2 Imaging Systems,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-PACK B12 Pretreatment Set- IVD for diagnostic use for pre-treatment...
The Issue: The AIA-2000 bar code scanners depend on the quiet zone to help identify the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Berman Angiographic Catheter 60cm Item Number: AI-07130-J Recalled by...
The Issue: Potential leak in the balloon extension line. If a leak was present and went...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Berman Angiographic Catheter 50cc Item Number: AI-07130 Recalled by...
The Issue: Potential leak in the balloon extension line. If a leak was present and went...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Precision Xtra Blood Glucose & Ketone Monitoring System Recalled by Abbott...
The Issue: Instructions sent in a letter or in instructions for use for disinfecting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optium EZ Blood Glucose Monitoring System Recalled by Abbott Diabetes Care,...
The Issue: Instructions sent in a letter or in instructions for use for disinfecting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FreeStyle Precision H Blood Glucose and Ketone Monitoring System Recalled by...
The Issue: Instructions sent in a letter or in instructions for use for disinfecting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.