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. 1,967 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
1,967 in last 12 months

Showing 1842118440 of 30,087 recalls

Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom OBSTETRICAL PACK convenience kits Recalled by Avid Medical,...

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom KNEE ARTHROSCOPY PACK convenience kits Recalled by Avid...

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Quidel Corporation

Recalled Item: InflammaDry(R) AN RPS DIAGNOSTIC SOLUTION Recalled by Quidel Corporation Due...

The Issue: In-house testing revealed the presence of plastic spurs at the tips of some...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Medtronic Perfusion Systems

Recalled Item: DLP Extension Line Adapters 20 in length Used to extend Recalled by...

The Issue: Identification of small pinholes in a single packaging configuration of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom MINOR PROCEDURE 6A convenience kits Recalled by Avid Medical,...

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom LAMINECTOMY PACK convenience kits Recalled by Avid Medical,...

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Medtronic Perfusion Systems

Recalled Item: DLP Pressure Monitoring Extension Line Adapters Extends the pressure line...

The Issue: Identification of small pinholes in a single packaging configuration of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· NeuroLogica Corporation

Recalled Item: The GC80 Digital X-ray Imaging System Recalled by NeuroLogica Corporation...

The Issue: An image was obtained with over exposure during a Thorax examination using...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom HEART CATH TRAY convenience kits Recalled by Avid Medical,...

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom GENERAL PACK convenience kits Recalled by Avid Medical, Inc....

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom SPINE convenience kits Recalled by Avid Medical, Inc. Due to...

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS MIS Screw 6.5 x 40mm. Part of MAXIMIS Recalled by Valorem...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Elekta, Inc.

Recalled Item: MOSAIQ(R) Oncology Information System Recalled by Elekta, Inc. Due to...

The Issue: Retention of Outdated Information in an Order Set. In the Care Plan Library,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· B. Braun Medical, Inc.

Recalled Item: Contiplex Nerve Block Tray. Product Catalog Number: 570205. Local anesthesia...

The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· B. Braun Medical, Inc.

Recalled Item: Pain Management Tray. Product Catalog Number: 560602. Local anesthesia of...

The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· B. Braun Medical, Inc.

Recalled Item: Pencan Spinal Needle Tray. Product Catalog Number: 333865. Local anesthesia...

The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· B. Braun Medical, Inc.

Recalled Item: Customer Epidural Anesthesia Tray. Product Catalog Number: 555234. Local...

The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· B. Braun Medical, Inc.

Recalled Item: Perifix FX Epidural Anesthesia Tray. Product Catalog Numbers: 551993...

The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· B. Braun Medical, Inc.

Recalled Item: Perifix Single Dose Epidural Anesthesia Tray. Product Catalog Number:...

The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· B. Braun Medical, Inc.

Recalled Item: PENCAN Spinal Anesthesia Tray. Product Catalog Number: 560590. Local...

The Issue: B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI...

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

Class II — Potential Health HazardOngoing