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. 1,146 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
1,146 in last 12 months

Showing 6481–6500 of 55,415 recalls

Medical DeviceMarch 26, 2024· Philips Respironics, Inc.

Recalled Item: BiPAP A40 Ventilators: BiPAP A40 Recalled by Philips Respironics, Inc. Due...

The Issue: Potential for devices to experience interruption/loss of therapy during a...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 25, 2024· SonarMed Inc

Recalled Item: AW-M0001 SONARMED MONITOR. Used in conjunction with SonarMed Acoustic...

The Issue: Software anomaly resulted in failure to detect a partial obstruction in 2.5...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 25, 2024· Ossur H / F

Recalled Item: RKN130002 Recalled by Ossur H / F Due to Due to firmware issues with the...

The Issue: Due to firmware issues with the prosthetic knee, there is the potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2024· Ossur H / F

Recalled Item: RKN130003 Recalled by Ossur H / F Due to Due to firmware issues with the...

The Issue: Due to firmware issues with the prosthetic knee, there is the potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2024· Ossur H / F

Recalled Item: RKNXC0003 Recalled by Ossur H / F Due to Due to firmware issues with the...

The Issue: Due to firmware issues with the prosthetic knee, there is the potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2024· Ossur H / F

Recalled Item: RKNXC0005 Recalled by Ossur H / F Due to Due to firmware issues with the...

The Issue: Due to firmware issues with the prosthetic knee, there is the potential for...

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

Class II — Potential Health HazardOngoing
DrugMarch 25, 2024· Amneal Pharmaceuticals of New York, LLC

Recalled Item: Methylergonovine Maleate Tablets Recalled by Amneal Pharmaceuticals of New...

The Issue: Failed Dissolution Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2024· Novitium Pharma LLC

Recalled Item: Digoxin Tablets Recalled by Novitium Pharma LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMarch 23, 2024· Aruba Aloe Balm N.V.

Recalled Item: Aruba Aloe Hand Sanitizer Gel Recalled by Aruba Aloe Balm N.V. Due to...

The Issue: Chemical Contamination: Product manufactured with ethanol API that contains...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
FoodMarch 23, 2024· The Coastal Companies DBA Hearn Kirkwood

Recalled Item: Egg salad sandwich packaged in clamshell for individual sale. 7.22oz...

The Issue: Tuna salad sandwich was mislabeled as an egg salad sandwich. There is an...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 23, 2024· Aruba Aloe Balm N.V.

Recalled Item: Alcoholada Gel Recalled by Aruba Aloe Balm N.V. Due to Chemical...

The Issue: Chemical Contamination: Product manufactured with ethanol API that contains...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 23, 2024· Philips Ultrasound, Inc.

Recalled Item: 5000 Compact Series Ultrasound Systems Recalled by Philips Ultrasound, Inc....

The Issue: Ultrasound system with: 1) transesophageal echocardiography transducer (TEE)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline medical procedure kits labeled as follows: a) CYSTO Recalled by...

The Issue: A slight dimensional variation which has the potential for increased...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2024· EBI, LLC

Recalled Item: Biomet OrthoPak Non-invasive Bone Growth Stimulator System-Indicated for the...

The Issue: Damage to the lead wire sheath (black cable) component and causing exposure...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: 1 Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to A slight...

The Issue: A slight dimensional variation which has the potential for increased...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline medical procedure kits labeled as follows: a) C-SECTION CDS Recalled...

The Issue: A slight dimensional variation which has the potential for increased...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline medical procedure kits labeled as follows: a) BASIC NASAL Recalled...

The Issue: A slight dimensional variation which has the potential for increased...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2024· EBI, LLC

Recalled Item: 48" Lead Wires Recalled by EBI, LLC Due to Damage to the lead wire sheath...

The Issue: Damage to the lead wire sheath (black cable) component and causing exposure...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline medical procedure kits labeled as follows: a) KIT CANISTER Recalled...

The Issue: A slight dimensional variation which has the potential for increased...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2024· Parker Laboratories, Inc.

Recalled Item: Redux Electrolyte Creme Recalled by Parker Laboratories, Inc. Due to Product...

The Issue: Product demonstrates low viscosity.

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

Class II — Potential Health HazardOngoing