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. 2,623 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
2,623 in last 12 months

Showing 1990119920 of 55,415 recalls

Medical DeviceApril 30, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Multi Display Manager in the Artis Systems (Image-Intensified Fluoroscopic...

The Issue: Artis systems containing a Multi Display Manager of a specific lot, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2020· GE Healthcare, LLC

Recalled Item: Giraffe Incubator with installed Servo Oxygen module. Infant incubator....

The Issue: Potential for certain Giraffe Incubators and Giraffe OmniBeds to deliver a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2020· GE Healthcare, LLC

Recalled Item: Giraffe OmniBed with installed Servo Oxygen module. Infant incubator and...

The Issue: Potential for certain Giraffe Incubators and Giraffe OmniBeds to deliver a...

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

Class II — Potential Health HazardOngoing
FoodApril 28, 2020· Glaxosmithkline Consumer Healthcare Holdings

Recalled Item: Benefiber Prebiotic Fiber Supplement Recalled by Glaxosmithkline Consumer...

The Issue: Fiber prebiotic product potentially contaminated with small plastic pieces

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 28, 2020· Glaxosmithkline Consumer Healthcare Holdings

Recalled Item: Benefiber Healthy Shape Prebiotic Fiber Supplement Recalled by...

The Issue: Fiber prebiotic product potentially contaminated with small plastic pieces

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 27, 2020· Philips North America, LLC

Recalled Item: Philips HeartStart MRx Monitor/Defibrillators Model numbers M3535A Recalled...

The Issue: HeartStart XL MonitorlDefibrillators may not have been included in prior...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2020· Defibtech, LLC

Recalled Item: DDU-2450 Lifeline ECG Model Numbers DDU-A2450EN DDU-E2450DE DDU-E2450EN...

The Issue: A component issue may cause the AED to abort a shock delivery or reset...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2020· Defibtech, LLC

Recalled Item: DDU-2300 Lifeline/ReviveR View Recalled by Defibtech, LLC Due to A component...

The Issue: A component issue may cause the AED to abort a shock delivery or reset...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2020· Defibtech, LLC

Recalled Item: DDU-2400EN Lifeline PRO Recalled by Defibtech, LLC Due to A component issue...

The Issue: A component issue may cause the AED to abort a shock delivery or reset...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: 1/4X3/8 REDUC CONN Recalled by LivaNova USA Inc. Due to The firm has...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Sterile Disposable Connectors ASY 1/2 CONN W/LL STRLE 24 REF/ Recalled by...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Vein Irrigation Cannula with blunt tip. ASY VIC Recalled by LivaNova USA...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Sterile Disposable Connectors ASY RDC Y 1/2X3/8X3/8 STR 24 REF/ Recalled by...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Sterile Disposable Connectors ASY STR CONN 1/4 STRLE 24. REF/ Recalled by...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Sterile Disposable Connectors ASY S CONN 3/16X1/8 RDR ANLD24 REF/ Recalled...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: 3/8X3/8X3/8 Y CONN Recalled by LivaNova USA Inc. Due to XXX

The Issue: XXX

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Sterile Disposable Connectors ASY CONN EQUAL 3/16 WYE 24 REF/ Recalled by...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· LivaNova USA Inc.

Recalled Item: Sterile Disposable Connectors ASY Y CONN 3/8 X 3/8 X Recalled by LivaNova...

The Issue: The firm has identified through internal tests that the sterile barrier of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· Physio-Control, Inc.

Recalled Item: Infant/Child Reduced Energy Defibrillation Electrodes Recalled by...

The Issue: Packaging of infant child reduced energy electrodes was not properly sealed.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2020· Physio-Control, Inc.

Recalled Item: Infant Child Starter Kits Recalled by Physio-Control, Inc. Due to Packaging...

The Issue: Packaging of infant child reduced energy electrodes was not properly sealed.

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

Class II — Potential Health HazardOngoing