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. 1,908 recalls have been distributed to Ohio in the last 12 months.
Showing 27841–27860 of 55,415 recalls
Recalled Item: Discovery IQ 2.0 20cm Recalled by GE Healthcare, LLC Due to Some CT and...
The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK Recalled by Sun...
The Issue: There is a potential for the patient port retaining ring to not fully seat...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CT Goldseal Optima CT 600 Recalled by GE Healthcare, LLC Due to Some CT and...
The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima CT 520 Recalled by GE Healthcare, LLC Due to Some CT and CT/PET...
The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAT-Check MANUAL RESUSCITATOR / VENTILATOR Recalled by Sun Med, LLC Due to...
The Issue: There is a potential for the patient port retaining ring to not fully seat...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK Recalled by Sun...
The Issue: There is a potential for the patient port retaining ring to not fully seat...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery MI Recalled by GE Healthcare, LLC Due to Some CT and CT/PET...
The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK Recalled by Sun...
The Issue: There is a potential for the patient port retaining ring to not fully seat...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery NM/CT 670 ES Recalled by GE Healthcare, LLC Due to When your...
The Issue: When your system was installed, the Main disconnect switch, EPO button on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery RT labeled as: a. MID BJG Recalled by GE Healthcare, LLC Due to...
The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CT Goldseal BrightSpeed 16 PWR TIO 2 YR Recalled by GE Healthcare, LLC Due...
The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery NM/CT 670 Pro Recalled by GE Healthcare, LLC Due to When your...
The Issue: When your system was installed, the Main disconnect switch, EPO button on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software Package Recalled by Beckman Coulter Inc. Due to Sorting-Drive...
The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK Recalled by Sun...
The Issue: There is a potential for the patient port retaining ring to not fully seat...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software Package Recalled by Beckman Coulter Inc. Due to Sorting-Drive...
The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sorting-Drive Professional Part Recalled by Beckman Coulter Inc. Due to...
The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reliance 1227 Cart and Utensil Washer/Disinfector Recalled by Steris...
The Issue: The firm has become aware that the Reliance 1227 Cart and Utensil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vertebral Motion Analyzer (VMA) Recalled by Ortho Kinematics, Inc Due to...
The Issue: This email is to provide notification that, due to a software bug that has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Collagen Reagent Recalled by Helena Laboratories, Corp. Due to Through an...
The Issue: Through an investigation, it has been determined that vials of Collagen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Platelet Aggregation Kit Recalled by Helena Laboratories, Corp. Due to...
The Issue: Through an investigation, it has been determined that vials of Collagen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.