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. 1,181 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
1,181 in last 12 months

Showing 1161–1180 of 30,087 recalls

Medical DeviceAugust 15, 2025· ETHICON, LLC

Recalled Item: STRATAFIX Spiral PDS Plus Bidirectional Knotless Tissue Control Device...

The Issue: Potential for barb non-engagement.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2025· Exactech, Inc.

Recalled Item: Exactech Equinoxe Recalled by Exactech, Inc. Due to Reverse Shoulder humeral...

The Issue: Reverse Shoulder humeral liners have an articular surface position outside...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Philips North America Llc

Recalled Item: Philips CT systems labeled as the following: 1. Ingenuity CT 728326 Recalled...

The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Philips North America Llc

Recalled Item: Philips CT systems labeled as the following: 1. Brilliance iCT Recalled by...

The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Philips North America Llc

Recalled Item: Philips CT systems labeled as the following: 1. IQon Spectral CT Recalled by...

The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Philips North America Llc

Recalled Item: Philips CT systems labeled as the following: 1. CT 6000 Recalled by Philips...

The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Philips North America Llc

Recalled Item: Philips CT systems labeled as the following: 1. Big Bore RT Recalled by...

The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Philips North America Llc

Recalled Item: Philips CT systems labeled as the following: 1. Ingenuity CT Family Brazil...

The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Philips North America Llc

Recalled Item: Philips CT systems labeled as the following: 1. Brilliance 16 Power Recalled...

The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Penner Patient Care, Inc.

Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...

The Issue: The device does not bear a unique device identifier.

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

Class III — Low RiskOngoing
Medical DeviceAugust 13, 2025· Philips North America Llc

Recalled Item: Philips CT systems labeled as the following: 1. Ingenuity Core128 Recalled...

The Issue: The patient support table (couch) may descend unexpectedly to the lowermost...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Beckman Coulter Inc.

Recalled Item: UniCel DxH 800 COULTER Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Hematology analyzers configured with HGB photometers may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Beckman Coulter Inc.

Recalled Item: UniCel DxH 690T COULTER Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Hematology analyzers configured with HGB photometers may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2025· Penner Patient Care, Inc.

Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...

The Issue: The device does not bear a unique device identifier.

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

Class III — Low RiskOngoing
Medical DeviceAugust 13, 2025· Penner Patient Care, Inc.

Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...

The Issue: The device does not bear a unique device identifier.

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

Class III — Low RiskOngoing
Medical DeviceAugust 13, 2025· Penner Patient Care, Inc.

Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...

The Issue: The device does not bear a unique device identifier.

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

Class III — Low RiskOngoing
Medical DeviceAugust 13, 2025· Penner Patient Care, Inc.

Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...

The Issue: The device does not bear a unique device identifier.

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

Class III — Low RiskOngoing
Medical DeviceAugust 13, 2025· Penner Patient Care, Inc.

Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...

The Issue: The device does not bear a unique device identifier.

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

Class III — Low RiskOngoing
Medical DeviceAugust 13, 2025· Penner Patient Care, Inc.

Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...

The Issue: The device does not bear a unique device identifier.

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

Class III — Low RiskOngoing
Medical DeviceAugust 13, 2025· Penner Patient Care, Inc.

Recalled Item: Penner Pacific Bathing Spa Recalled by Penner Patient Care, Inc. Due to The...

The Issue: The device does not bear a unique device identifier.

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

Class III — Low RiskOngoing