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. 1,888 recalls have been distributed to Ohio in the last 12 months.
Showing 30021–30040 of 30,087 recalls
Recalled Item: Mercury Spinal System DIA 5.5 x 110mm Straight Rod Recalled by Spinal...
The Issue: Spinal Elements has initiated a recall for the Mercury Spinal System due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mercury Spinal System DIA 5.5 x 60 MM Lordosed Rod Recalled by Spinal...
The Issue: Spinal Elements has initiated a recall for the Mercury Spinal System due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mercury Spinal System DIA 5.5 x 40 MM Lordosed Rod Recalled by Spinal...
The Issue: Spinal Elements has initiated a recall for the Mercury Spinal System due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mercury Spinal System DIA 5.5 x 40mm Straight Rod Recalled by Spinal...
The Issue: Spinal Elements has initiated a recall for the Mercury Spinal System due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sunquest Encompass The reporting site is using the Encompass software...
The Issue: Sunquest is recalling the Sunquest Encompass versions 2.4 and later because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Harmonie software versions 5.1 uo to 6.2e : Harmonie-E Long Recalled by...
The Issue: The firm is initiating this recall because the implied or stated indications...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: lnvatec SpA brand Diver C.E. Recalled by Invatec Llc Due to Devices labeled...
The Issue: Devices labeled for an intended use was not included in the existing 510(k)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IF 8000 Recalled by Zynex Medical, Inc. Due to Zynex notified customers that...
The Issue: Zynex notified customers that a malfunction in the IF 8000 can result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7.5mm x 50mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7.5mm x 40mm Noncannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5mm x 35mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5mm x 30mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7.5mm x 30mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5mm x 40mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7.5mm x 40mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5.5mm x 40mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5.5mm x 30mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.5mm x 40mm Noncannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5.5mm x 50mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5mm x 50mm Noncannulated Screw Shank Subsequent Codes: KWP Recalled by...
The Issue: The tulip portion of the screw assembly can disengage from the shank after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.