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. 1,943 recalls have been distributed to Ohio in the last 12 months.
Showing 23061–23080 of 30,087 recalls
Recalled Item: Siemens Symbia T Series Recalled by Siemens Medical Solutions USA, Inc. Due...
The Issue: Fuses with the improper amperage rating were installed in the Symbia S,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PICC Kits with Peel-Away Sheath Component Recalled by Arrow International...
The Issue: the catheter peel-away component hub tabs may prematurely detach. One injury...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow International Recalled by Arrow International Inc Due to saline...
The Issue: saline leakage from unsecured connections between the Touhy Borst adaptor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AU680 Chemistry Analyzers Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman coulter has received complaints regarding leaking and cracked C...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AU5800 Chemistry Analyzers Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman coulter has received complaints regarding leaking and cracked C...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AU480 Chemistry Analyzers Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman coulter has received complaints regarding leaking and cracked C...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software version 4.44A utilized on the BD MAX System Recalled by BD LIFE...
The Issue: The BD MAX System software version 4.44A contains a software anomaly that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaPlus Trach Care* Closed Suction System for Adults Recalled by Halyard...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaPlus Trach Care* Closed Suction System for Adults Recalled by Halyard...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Wet Pak* Closed Suction System for Adults Recalled by Halyard...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Wet Pak* Closed Suction System for Pediatrics Recalled by Halyard...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Closed Suction System for Neonates/Pediatrics Recalled by Halyard...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Sciatic Nerve Retractor and Sciatic Nerve Retractor Long Recalled by...
The Issue: Potential for micropores to form, allowing fluid to enter the hollow handle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Multi-Access Port Closed Suction System for Adults Recalled by...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Multi-Access Port Replacement Catheter for Adults Recalled by...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.