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. 2,786 recalls have been distributed to Ohio in the last 12 months.
Showing 4861–4880 of 30,087 recalls
Recalled Item: Medtronic Duet External Drainage and Monitoring System Recalled by Medtronic...
The Issue: Potential for catheter disconnection from the patient line stopcock connectors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Duet External Drainage and Monitoring System Recalled by Medtronic...
The Issue: Potential for catheter disconnection from the patient line stopcock connectors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Epidural tray. PERIFIX 17 Ga. x 3-1/2 in. (90 mm) Tuohy Recalled by B. Braun...
The Issue: Kits should contain Filter Straws with Standard Luer Connections however,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Epidural tray. PERIFIX 17 Ga. x 3-1/2 in. (90 mm) Tuohy Recalled by B. Braun...
The Issue: Kits should contain Filter Straws with Standard Luer Connections however the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TrueDent Clear Recalled by STRATASYS LTD Due to Customers unable to use...
The Issue: Customers unable to use cartridges due to formatting error in expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TrueDent Yellow Recalled by STRATASYS LTD Due to Customers unable to use...
The Issue: Customers unable to use cartridges due to formatting error in expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TrueDent Cyan Recalled by STRATASYS LTD Due to Customers unable to use...
The Issue: Customers unable to use cartridges due to formatting error in expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TrueDent Magenta Recalled by STRATASYS LTD Due to Customers unable to use...
The Issue: Customers unable to use cartridges due to formatting error in expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TrueDent White Recalled by STRATASYS LTD Due to Customers unable to use...
The Issue: Customers unable to use cartridges due to formatting error in expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : INS5HND / Integra Cranial access kit (without Prep Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : HITHSP04 / Integra Cranial Access Kit. For access Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : INS7260 / Integra¿ Cranial Access Kit. For access Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : INS7270 / Integra¿ Cranial Access Kit. For access Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : INS7250 / Integra Cranial Access Kit. For access Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : 31156 / COMBO KIT CONTAINS INS-8301 Recalled by Integra LifeSciences Corp....
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INS7280 / Integra¿ Cranial Access Kit. For access to the Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : INSHITHND / Integra¿ Cranial access kit (without Prep Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : HITHSP06 / Integra Cranial Access Kit. For access Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : INSHITH / Integra¿ Cranial Access Kit. For access Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: : INSHITHRZN / Integra Cranial Access Kit. For access Recalled by Integra...
The Issue: A defect in the sterile packaging (header bag) of the Cranial Access Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.