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. 1,967 recalls have been distributed to Ohio in the last 12 months.
Showing 17101–17120 of 30,087 recalls
Recalled Item: PTS Panels¿ CHOL+GLU Test Strips () Recalled by Polymer Technology Systems,...
The Issue: Potential for loss of activity of the glucose analyte (under-recovery) prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray BCID Panel (Blood Culture Identification Panel) Recalled by...
The Issue: There is an increased risk of false positive Proteus results when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Prestige LP(TM) Cervical Disc System with Streamlined Instruments...
The Issue: The firm received complaints of drill bits breaking during use with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesis Surgical Cassette Tapered Implants are intended for placement...
The Issue: The surgical cassette contained extra-large white grommets making the 3.8 mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Cardiology Hemo Recalled by McKesson Israel Ltd. Due to Change...
The Issue: Change Healthcare has identified an issue where, under certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vacuum Regulator Recalled by Ohio Medical Corporation Due to Final quality...
The Issue: Final quality control testing was not completed before the devices were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fischer Cone Biopsy Excisor Recalled by CooperSurgical, Inc. Due to Products...
The Issue: Products have been packaged with an incorrect product size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton-C2 Ventilator Unit Intended to provide ventilator support to adults...
The Issue: After two and a half years, the battery fuel gauge may indicate a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5 mm Apple-Hunt Secondary Cannula/Pyramidal Tip Trocar - extended length...
The Issue: Products have been packaged with the wrong Trocar length type.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hinge Coupling Hoffmann LRF Catalog # 4933-0-800 Intended for fixation...
The Issue: The wrong parts were picked for packaging. The connecting Nuts were packed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power-LOAD Cot Fastening System Recalled by Stryker Medical Division of...
The Issue: The power load floor plates which hold the ambulance cot anchors in place...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton-C3 Ventilator Unit Intended to provide ventilator support to adults...
The Issue: After two and a half years, the battery fuel gauge may indicate a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phoenix Nail System Recalled by Zimmer Biomet, Inc. Due to Certain lots of...
The Issue: Certain lots of the Phoenix Tibia Nail 3.5mm Inserter instruments are being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences EZ Glide Aortic Cannula Recalled by SPS Sterilization,...
The Issue: The expiration date on the device labeling exceeds its actual validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Femoral Venous Cannula Recalled by SPS Sterilization,...
The Issue: The expiration date on the device labeling exceeds its actual validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Thin-Flex Single Stage Venous Drainage Cannula Recalled...
The Issue: The expiration date on the device labeling exceeds its actual validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Avid Dual Stage Venous Drainage Cannula Recalled by SPS...
The Issue: The expiration date on the device labeling exceeds its actual validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Thin-Flex Single Stage Venous Drainage Cannula Recalled...
The Issue: The expiration date on the device labeling exceeds its actual validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Aortic Perfusion Cannula Recalled by SPS Sterilization,...
The Issue: The expiration date on the device labeling exceeds its actual validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Wallstent Endoprosthesis Tracheobronchial Transhepatic...
The Issue: The expiration date on the device labeling exceeds its actual validated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.