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 22361–22380 of 30,087 recalls
Recalled Item: Servo Humidifier 163 Recalled by Teleflex Medical Due to Cracks may occur at...
The Issue: Cracks may occur at the 15mm and 22mm ISO female connector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Position Pro Mattress. Mattress Recalled by Stryker Medical Division...
The Issue: Potential for power cord to melt; hazards include electric shock and fire.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...
The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...
The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...
The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...
The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gynecare Thermachoice III Uterine Balloon Therapy System Ethicon Recalled by...
The Issue: Stability data does not substantiate the labeled two-year shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VS200 radiographic Cassette Holder or Wall Stand. For use in Recalled by Del...
The Issue: The wall stand cassette holder can suddenly fall to the bottom of its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...
The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VS300 radiographic Cassette Holder or Wall Stand. For use in Recalled by Del...
The Issue: The wall stand cassette holder can suddenly fall to the bottom of its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Model 3500 and 4000 Syringe Infusion Pumps and Medfusion Recalled...
The Issue: There have been intermittent issues with Supercap POST (power on self-test)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Best Practice Kits containing certain production lots of Endo GIA Recalled...
The Issue: Staplers fail to fire or partially fire and reports of the instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Endo GIA Ultra Universal 12 mm Short Stapler Handle Recalled by...
The Issue: Staplers fail to fire or partially fire and reports of the instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ergon 2 Articulating Equipment Boom Monitor Brackets mounting point for...
The Issue: The hardware that holds the VESA plate and the display interface / monitor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Green Mamba Suture Passer Recalled by Biomet, Inc. Due to There may be a...
The Issue: There may be a separation and an insufficient weld between the spring and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRN 50-M+ Recalled by Gsi Group Inc Due to The item was recalled due to an...
The Issue: The item was recalled due to an increased user/patient risk of exposure to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Endo GIA Ultra Universal Standard Stapler Handle Recalled by...
The Issue: Staplers fail to fire or partially fire and reports of the instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Black Mamba Suture Passer Recalled by Biomet, Inc. Due to There may be a...
The Issue: There may be a separation and an insufficient weld between the spring and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Endo GIA Ultra Universal 12 mm XL Stapler Handle Recalled by...
The Issue: Staplers fail to fire or partially fire and reports of the instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CNSystems TASK FORCE MONITOR 3040i Recalled by Partners In Medicine Llc Due...
The Issue: Device non-conformity which may lead to an incorrect oscillometric...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.