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. 1,148 recalls have been distributed to Ohio in the last 12 months.
Showing 4121–4140 of 30,087 recalls
Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HA FlexTrak-Patient transport functionality to transport the patient from...
The Issue: Oil may leak from the HA FlexTrack Trolley onto the floor when pressing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLIXENE Recalled by Atrium Medical Corporation Due to Complaints of reported...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLIXENE Recalled by Atrium Medical Corporation Due to Complaints of reported...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLIXENE Recalled by Atrium Medical Corporation Due to Complaints of reported...
The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Interventional Hemodynamic Application R.1.2X Recalled by PHILIPS...
The Issue: Potential for pressure wave data synchronization from two devices may not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis: MedStation ES (Main) Recalled by CareFusion 303, Inc. Due to If...
The Issue: If automated dispensing cabinets have specific software versions, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The D*Clot¿ HD Rotational Thrombectomy System is a percutaneous...
The Issue: Internal product testing failed bubble leak testing (ASTM F2096), which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZOLL 731 Ventilator (EMV+ Recalled by ZOLL Medical Corporation Due to...
The Issue: Operator's Guide & Quick Guide (QRG) ZOLL 731 Ventilator for MRI Compatible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE STERILE IRIS SCISSORS CVD/STD (case) and DYNJ04049H Recalled by...
The Issue: There is the potential of the tip protector to fall off 4.5" sterile,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TabloCart with Prefiltration Drawer PN-0006813 Recalled by Outset Medical,...
The Issue: A cart with prefiltration drawer, an optional hemodialysis system accessory,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Ultra 8 IAB Intra-Aortic Balloon Catheter Kit Recalled by ARROW...
The Issue: Teleflex received reports indicating an infrequent condition that, when not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.