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. 1,094 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
1,094 in last 12 months

Showing 16421–16440 of 30,087 recalls

Medical DeviceJune 21, 2018· Ossur Americas

Recalled Item: Ossur Skull Pin Recalled by Ossur Americas Due to Halo system products...

The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Ossur Americas

Recalled Item: Ossur Recalled by Ossur Americas Due to Halo system products labeled MR...

The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Ossur Americas

Recalled Item: Ossur CB Resolve Recalled by Ossur Americas Due to Halo system products...

The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Ossur Americas

Recalled Item: Ossur OB Resolve Recalled by Ossur Americas Due to Halo system products...

The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Ossur Americas

Recalled Item: Ossur Skull Pin Recalled by Ossur Americas Due to Halo system products...

The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Ossur Americas

Recalled Item: Ossur Recalled by Ossur Americas Due to Halo system products labeled MR...

The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Ossur Americas

Recalled Item: Ossur Recalled by Ossur Americas Due to Halo system products labeled MR...

The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Ossur Americas

Recalled Item: Ossur Recalled by Ossur Americas Due to Halo system products labeled MR...

The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Degania Silicone, Ltd.

Recalled Item: Temperature Sensor Catheter 8FR Recalled by Degania Silicone, Ltd. Due to...

The Issue: The catheters are suspected to contain defective sensors; if used, defective...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2018· Degania Silicone, Ltd.

Recalled Item: Thermistor Foley catheter Recalled by Degania Silicone, Ltd. Due to The...

The Issue: The catheters are suspected to contain defective sensors; if used, defective...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2018· Vyaire Medical

Recalled Item: The Tri-Flo Subglottic Suction System Recalled by Vyaire Medical Due to...

The Issue: Vyaire Medical has discovered potential patient safety risk with associated...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 20, 2018· Boston Scientific Corporation

Recalled Item: Boston Scientific Maestro 4000 Cardiac Ablation System Recalled by Boston...

The Issue: Reports of unintended continuation of radiofrequency (RF) energy delivery...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2018· Espiner Medical Ltd

Recalled Item: Espiner Tissue Retrieval System-Eco-Sac Trocar 12mm Vol: 1200 ml...

The Issue: Label was incorrect. The label states that the volume of the retrieval bag...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2018· Nico Corp.

Recalled Item: NICO Shepherd' s Hook - Greenberg Recalled by Nico Corp. Due to Mislabeling

The Issue: Mislabeled hook pouch included a transport/storage label rather than the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2018· Stryker Sustainability Solutions

Recalled Item: Reprocessed Xcel Bladeless Trocar (H12LP) Model # H12LP Reprocessed...

The Issue: Through investigation, it was determined that H12LP Trocars in scope of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2018· Zimmer Biomet, Inc.

Recalled Item: Connecting Bolt Recalled by Zimmer Biomet, Inc. Due to Product was...

The Issue: Product was manufactured from the incorrect material, which shows a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2018· Bovie Medical Corporation

Recalled Item: J-Plasma Precise 360 Recalled by Bovie Medical Corporation Due to There is a...

The Issue: There is a potential risk associated with the PEEK tip of the J-Plasma...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2018· Compass Health Brands (Corporate Office)

Recalled Item: CPAP Mask Cushion Recalled by Compass Health Brands (Corporate Office) Due...

The Issue: A May 2015 design change in the cushion seal replacement part and...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 18, 2018· Beaver Visitec

Recalled Item: Slit Knife 2.6mm 45degree Bevel Up Recalled by Beaver Visitec Due to Mislabeling

The Issue: Mislabel of product 373726 Lot 6001700 with 374891 Lot 6001701 on individual...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2018· Hitachi Medical Systems America Inc

Recalled Item: Hitachi Oasis MRI system Product Usage: Hitachi MR system is Recalled by...

The Issue: The stainless steel belt which runs the length of the table underneath the...

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

Class II — Potential Health HazardOngoing