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. 2,738 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
2,738 in last 12 months

Showing 1130111320 of 55,415 recalls

Medical DeviceNovember 21, 2022· Leica Microsystems, Inc.

Recalled Item: Leica MICROSYSTEMS Proveo 8 Recalled by Leica Microsystems, Inc. Due to...

The Issue: There is a potential issue resulting in the Power Supply potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2022· BioReference Health, LLC

Recalled Item: The 4Kscore Test is an in vitro serum or plasma Recalled by BioReference...

The Issue: SPM software anomalies that may lead to the generation of erroneous 4Kscore...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Presource Packs IV START TRAY I-Intended for IV Recalled by...

The Issue: Presource Kits contains the ICU MicroClave Clear Connector due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Presource Packs IV START KIT-Intended for IV Access Recalled...

The Issue: Presource Kits contains the ICU MicroClave Clear Connector due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2022· Cardinal Health 200, LLC

Recalled Item: Cardinal Health Presource Packs IV START KIT- Intended for IV Recalled by...

The Issue: Presource Kits contains the ICU MicroClave Clear Connector due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2022· Ventana Medical Systems, Inc.

Recalled Item: VENTANA PD-L1 (SP142) VENTANA PD-L1 (SP142) Assay (Class III Recalled by...

The Issue: Internal comparison studies revealed unacceptable, light staining. Light...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline CISION Sterile Blades. Labeled as follows with corresponding Item...

The Issue: Potential of the blade puncturing the outer foil layer causing a breach in...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2022· DeVilbiss Healthcare LLC

Recalled Item: DeVilbiss Recalled by DeVilbiss Healthcare LLC Due to The firm has received...

The Issue: The firm has received complaints of the device becoming hot. The firm has...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2022· Natus Medical Incorporated

Recalled Item: The Natus Cranial Access Kit is designed to be a complete Recalled by Natus...

The Issue: Due to Cranial Access Kits containing recalled sterile surgical drapes. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2022· ConMed Corporation

Recalled Item: Foot Controlled Electrosurgical Suction Coagulator Recalled by ConMed...

The Issue: Suction ports may potentially be occluded on the affected devices. If this...

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

Class II — Potential Health HazardOngoing
FoodNovember 17, 2022· GREEN DAY PRODUCE

Recalled Item: Enoki Mushroom Net wt. 200g (7.05 oz.) 25 units per Recalled by GREEN DAY...

The Issue: Product found to be contaminated with Listeria monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 17, 2022· Amys Kitchen Inc

Recalled Item: Amy's Kitchen Gluten Free Bean and Cheese Burrito 5.5 oz. Recalled by Amys...

The Issue: Product may contain foreign material: pieces of plastic

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 17, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Sterile Procedural Tray Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: Sterile blades within sterile kits have the potential for the blade to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Sterile Procedural Trays Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: Sterile blades within sterile kits have the potential for the blade to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Sterile Procedural Trays Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: Sterile blades within sterile kits have the potential for the blade to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Sterile Procedural Trays Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: Sterile blades within sterile kits have the potential for the blade to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: UNIVERSAL CORE DR RUNNELS PACK. Sterile Procedural Tray Recalled by MEDLINE...

The Issue: Sterile blades within sterile kits have the potential for the blade to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Sterile Procedural Trays Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: Sterile blades within sterile kits have the potential for the blade to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Sterile Procedural Trays Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: Sterile blades within sterile kits have the potential for the blade to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Sterile Procedural Trays Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: Sterile blades within sterile kits have the potential for the blade to...

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

Class II — Potential Health HazardOngoing