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. 1,094 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
1,094 in last 12 months

Showing 17241–17260 of 55,415 recalls

Medical DeviceMarch 8, 2021· Arrow International Inc

Recalled Item: Arrow OnControl Bone Lesion Biopsy System Tray-11 ga 10 cm Recalled by Arrow...

The Issue: Difficulty inserting the biopsy ejector rod into the bone lesion biopsy...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK Iperia 7 Recalled by BIOTRONIK Inc Due to There is a potential for...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK ITREVIA 7 Recalled by BIOTRONIK Inc Due to There is a potential...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK INVENTRA 7 Recalled by BIOTRONIK Inc Due to There is a potential...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK INVENTRA 7 Recalled by BIOTRONIK Inc Due to There is a potential...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK Iforia 7 Recalled by BIOTRONIK Inc Due to There is a potential for...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK ITREVIA 7 Recalled by BIOTRONIK Inc Due to There is a potential...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK Ilestro 7 DR-T Recalled by BIOTRONIK Inc Due to There is a...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK ILIVIA 7 Recalled by BIOTRONIK Inc Due to There is a potential for...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2021· BIOTRONIK Inc

Recalled Item: BIOTRONIK ITREVIA 7 Recalled by BIOTRONIK Inc Due to There is a potential...

The Issue: There is a potential for premature battery depletion in Implantable...

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

Class II — Potential Health HazardOngoing
FoodMarch 8, 2021· New Generation Wellness Inc.

Recalled Item: Live Better vegan vitamin d-3 by CVS Health Recalled by New Generation...

The Issue: Vitamin D3 stability sample analyzed and found to be less than 100% of label...

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

Class III — Low RiskOngoing
Refund
FoodMarch 8, 2021· New Generation Wellness Inc.

Recalled Item: VEGAN VITAMIN D3 Recalled by New Generation Wellness Inc. Due to Vitamin D3...

The Issue: Vitamin D3 stability sample analyzed and found to be less than 100% of label...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 5, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA 2120i with Single Aspirate Autosampler (SMN 10488923) - OUS Recalled...

The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA 2120 SAA AUTOSAMPLER (SMN 10374453) - OUS Recalled by Siemens...

The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA 2120i (RoHS) Dual Aspirate Autosampler (SMN 11219530) - US Recalled by...

The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA 2120i Dual Aspirate (SMN 11314045) - US Recalled by Siemens Healthcare...

The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA 2120i Dual Aspirate (SMN 11314045) - OUS Recalled by Siemens...

The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2021· Covidien

Recalled Item: Covidien Surgiwand" II Suction and Irrigation Device: Electrosurgical...

The Issue: Investigations related to customer complaints received for particulate...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA 2120 DAA AUTOSAMPLER (SMN 10374454) - OUS Recalled by Siemens...

The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA 2120i Dual Aspirate Autosampler (SMN 10285573) - OUS Recalled by...

The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes

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

Class II — Potential Health HazardOngoing