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. 2,122 recalls have been distributed to Ohio in the last 12 months.
Showing 6721–6740 of 55,415 recalls
Recalled Item: NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product...
The Issue: The expiration date was not printed on the outer shipping label, leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IBA Proton Therapy System - PROTEUS 235 Recalled by Ion Beam Applications...
The Issue: There is a risk of mistreatment as irradiation is not prevented when some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product...
The Issue: The expiration date was not printed on the outer shipping label, leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-Guide Handpiece Adaptor Sleeve 3 Recalled by X-NAV Technologies, LLC Due...
The Issue: The Handpiece Adaptor may have a manufacturing defect causing incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product...
The Issue: The expiration date was not printed on the outer shipping label, leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thoratec HeartMate 3 Recalled by Thoratec Corp. Due to Potential for a leak...
The Issue: Potential for a leak path at the seal interface between the left ventricle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 25-LHP-828 Recalled by PACIFIC LASERTECH, LLC Due to These laser products...
The Issue: These laser products fail to comply with 21 CFR 1040.10(f)(4) Key control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: N-LHP-928 Recalled by PACIFIC LASERTECH, LLC Due to These laser products...
The Issue: These laser products fail to comply with 21 CFR 1040.10(f)(4) Key control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 25-LHP-928 Recalled by PACIFIC LASERTECH, LLC Due to These laser products...
The Issue: These laser products fail to comply with 21 CFR 1040.10(f)(4) Key control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peel-Away Introducer - Intended for the percutaneous introduction of balloon...
The Issue: Packaging may have low seal strength and not meet peel strength...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dilator - Intended to be used for dilating puncture sites Recalled by Cook...
The Issue: Packaging may have low seal strength and not meet peel strength...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Entuit Secure Adjustable Gastrointestinal Suture Anchor Set - Intended for...
The Issue: Packaging may have low seal strength and not meet peel strength...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Yueh Centesis Disposable Catheter Needle - Intended for use in Recalled by...
The Issue: Packaging may have low seal strength and not meet peel strength...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trocar Needle - Used for dilating puncture sites or catheter Recalled by...
The Issue: Packaging may have low seal strength and not meet peel strength...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mojo Full Face with Headgear Recalled by SleepNet Corporation Due to Update...
The Issue: Update to contraindications and warning language due to CPAP masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phantom 2 Nasal Vented Mask Recalled by SleepNet Corporation Due to Update...
The Issue: Update to contraindications and warning language due to CPAP masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mojo 2 Full Face Vented Mask Recalled by SleepNet Corporation Due to Update...
The Issue: Update to contraindications and warning language due to CPAP masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thoratec HeartMate 3 Recalled by Thoratec Corp. Due to Potential for a leak...
The Issue: Potential for a leak path at the seal interface between the left ventricle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mojo Non Vented Full Face Mask with Headgear Recalled by SleepNet...
The Issue: Update to contraindications and warning language due to CPAP masks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Cholestech LDX Battery Kit Recalled by Alere San Diego, Inc. Due to...
The Issue: There is a potential that the Cholestech LDX battery (an external battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.