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. 2,580 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
2,580 in last 12 months

Showing 2784127860 of 55,415 recalls

Medical DeviceMay 24, 2018· Draeger Medical, Inc.

Recalled Item: Fabius GS Tiro Anesthesia Machine Recalled by Draeger Medical, Inc. Due to...

The Issue: The Draeger anesthesia device may be able to dose 100% N2O. In the event of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· Draeger Medical, Inc.

Recalled Item: Fabius GS MRI Anesthesia Machine Recalled by Draeger Medical, Inc. Due to...

The Issue: The Draeger anesthesia device may be able to dose 100% N2O. In the event of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· Sun Med, LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· Draeger Medical, Inc.

Recalled Item: Apollo Anesthesia Machine Recalled by Draeger Medical, Inc. Due to The...

The Issue: The Draeger anesthesia device may be able to dose 100% N2O. In the event of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· Sun Med, LLC

Recalled Item: MEDLINE ADULT MANUAL RESUSCITATOR WITH LARGE ADULT MASK Recalled by Sun Med,...

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· Sun Med, LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· Sun Med, LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· Sun Med, LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· Sun Med, LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· Sun Med, LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· Sun Med, LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· Sun Med, LLC

Recalled Item: MEDLINE ADULT MANUAL RESUSCITATOR WITH MEDIUM ADULT MASK 5 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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· Sun Med, LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· Sun Med, LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· Sun Med, LLC

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.

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· Sun Med, LLC

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.

Class II — Potential Health HazardOngoing
FoodMay 23, 2018· Divvies LLC

Recalled Item: simply delicious Divvies SEMI-SWEET PEPPERMINT BARS made to share CHOCOLATE...

The Issue: Product may contain traces of milk.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 23, 2018· Helena Laboratories, Corp.

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.

Class III — Low RiskOngoing
Medical DeviceMay 23, 2018· Helena Laboratories, Corp.

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.

Class III — Low RiskOngoing
Medical DeviceMay 23, 2018· Ortho Kinematics, Inc

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.

Class II — Potential Health HazardOngoing