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. 1,932 recalls have been distributed to Ohio in the last 12 months.
Showing 24841–24860 of 30,087 recalls
Recalled Item: MX 16-slice CT Scanner System and MX 16-slice CT Scanner Recalled by Philips...
The Issue: "The orientation of images is displayed incorrectly. When operator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur (including ) Professional use in a laboratory for Recalled by...
The Issue: A slight crack of the tubing at the connecting fitting on the reservoir...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur XP Immunoassay System (including ) Professional use in...
The Issue: A slight crack of the tubing at the connecting fitting on the reservoir...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TITAN Operating Room Table Patient positioning during surgery Recalled by...
The Issue: Unintended movement of the operating table during surgical cases due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Stemmed 5 Degree Cemented Tibia Product Usage: This device Recalled...
The Issue: Cleaning process validation failure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elite XPL (Pulsed Light) Handpiece for the Cynosure Elite MPX Laser System...
The Issue: If the laser system is turned on and the user adjusts, installs or removes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker SmartLife Large Aseptic Housing Rx Only The Recalled by Stryker...
The Issue: The SmartLife Aseptic Housings are being recalled in that the top section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard¿ PerFix Light Plug The Bard¿ PerFix Light Plug is Recalled by Davol,...
The Issue: The patient record peel-off label product code and size did not match the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Box Label: 3 mm Cueva Electrode Kit Recalled by Ad-Tech Medical Instrument...
The Issue: The recall has been initiated due to concerns that the applicator wand may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker SmartLife Small Aseptic Housing Rx Only The Recalled by Stryker...
The Issue: The SmartLife Aseptic Housings are being recalled in that the top section of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RESTORIS PST Acetabular Straight Shell Impactors An impactor is a Recalled...
The Issue: MAKO has identified the potential that the shell impactors may be damaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RESTORIS PST Acetabular Offset Shell Impactors An impactor is a Recalled by...
The Issue: MAKO has identified the potential that the shell impactors may be damaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Persona Tibial Articular Surface Inserter is a sterilizable instrument...
The Issue: Affected product did not undergo heat treatment hardening step leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mortara Surveyor S12 and Surveyor S19 Patient Monitors. Product Usage:...
The Issue: Martara Instrument, Inc. has recently became aware of a potential safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RESTORIS PST Straight Shell Inserter An impactor is a reusable Recalled by...
The Issue: MAKO has identified the potential that the shell impactors may be damaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DPM 6 Patient Monitor and DPM 7 Patient Monitor. The Recalled by Mindray DS...
The Issue: Mindray has identified an issue that involves the IBP module used with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Specialty Audible Torque Wrench Mfg by: Stryker Spine Recalled by Stryker...
The Issue: Stryker has received a complaint from customers relating to a fracture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HomeChoice Automated PD system and HomeChoice Pro Automated PD system...
The Issue: There are additional and updated warning and cautions that are not in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accusorb MRI MAC7010 Product Usage: Radio frequency shielding blankets and...
The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accusorb MRI MAC7030 Product Usage: Radio frequency shielding blankets and...
The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.