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. 2,812 recalls have been distributed to Ohio in the last 12 months.
Showing 261–280 of 30,087 recalls
Recalled Item: Portex Spinal Tray Recalled by ICU Medical Inc. Due to Affected lots of...
The Issue: Affected lots of syringes may have a crack on the syringe collar, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rifton Equipment Recalled by Community Products, LLC Due to Potential for...
The Issue: Potential for fraying on the body support strap.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rifton Equipment Recalled by Community Products, LLC Due to Potential for...
The Issue: Potential for fraying on the body support strap.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gelsoft Plus Recalled by Vascutek, Ltd. Due to Gelatin sealed woven...
The Issue: Gelatin sealed woven polyester prostheses devices, designed for vascular...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rifton Equipment Recalled by Community Products, LLC Due to Potential for...
The Issue: Potential for fraying on the body support strap.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fixone Biocomposite Anchor Recalled by Aju Pharm Co., Ltd. Due to Reports of...
The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fixone Hybrid Anchor Recalled by Aju Pharm Co., Ltd. Due to Reports of...
The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesis Screw-In Anchor Recalled by Aju Pharm Co., Ltd. Due to Reports of...
The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AlternatiV+ Screw-In Anchor Recalled by Aju Pharm Co., Ltd. Due to Reports...
The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesis Knotless Anchor Recalled by Aju Pharm Co., Ltd. Due to Reports of...
The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesis Push-In Suture Anchor Recalled by Aju Pharm Co., Ltd. Due to Reports...
The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AlternatiV+ Max Knotless Anchor Recalled by Aju Pharm Co., Ltd. Due to...
The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesis Dual Thread Screw-In Anchor Recalled by Aju Pharm Co., Ltd. Due to...
The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. Recalled by...
The Issue: There may be voids located in the seal of Tyvek pouches associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rumex Disposable Diamond Dusted ILM Elevator Recalled by Vortex Surgical...
The Issue: There may be voids located in the seal of Tyvek pouches associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volk Single Use Vitrectomy Lenses 1. Flat Vitrectomy Lens Recalled by Vortex...
The Issue: There may be voids located in the seal of Tyvek pouches associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex Disposable Forceps and Cannula 1. 23GA ACTU8 Forceps Adaptive...
The Issue: There may be voids located in the seal of Tyvek pouches associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex Surgical 25GA Backflush Recalled by Vortex Surgical Inc. Due to There...
The Issue: There may be voids located in the seal of Tyvek pouches associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oertli 1. 23G Laser Probe OS4 Flex-Tip VK401113 2. 23G Recalled by Vortex...
The Issue: There may be voids located in the seal of Tyvek pouches associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 25GA Subretinal Injection Cannula VS0220.25 Recalled by Vortex Surgical Inc....
The Issue: There may be voids located in the seal of Tyvek pouches associated with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.