Product Recalls in Oklahoma

Product recalls affecting Oklahoma — including food, drugs, consumer products, medical devices, and vehicles distributed to Oklahoma. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,566 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,566 in last 12 months

Showing 1612116140 of 28,654 recalls

Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: BioFlo Midline 5F DL-20cm Max Sterile Barrier Drape Kit w/ Recalled by...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Bio-Stable 5F DL-55CM MST-70 KIT Non-Valved PG Recalled by Angiodynamics...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: XCELA PASV 5F SL 55CM IR-145 Nitinol Wire KIT PG Recalled by Angiodynamics...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Bio-Stable 5F SL-55CM IR-145 Kit Valved with Nitinol GW PG Recalled by...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Mako Surgical Corporation

Recalled Item: Rio System Irrigation Clip - Catalog # 111690 Product Usage: Recalled by...

The Issue: Out of tolerance.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Bio-Stable 5F DL-55CM IR-145 Kit Non-Valved with Nitinol GW PG Recalled by...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Zimmer Dental Inc

Recalled Item: Outer Package Label: Tapered Screw-Vent Implant System Recalled by Zimmer...

The Issue: Dental implants have incorrect item/lot numbers and size on the inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: CAN 5F SINGLE XCELA PICC Recalled by Angiodynamics Inc. (Navilyst Medical...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: RS 5F DL XPP KIT Recalled by Angiodynamics Inc. (Navilyst Medical Inc.) Due...

The Issue: A component of the kits might contain unsafe levels of bacterial endotoxins...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· FHC, Inc.

Recalled Item: microTargeting" STar" Drive System (Motorized) Recalled by FHC, Inc. Due to...

The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· FHC, Inc.

Recalled Item: microTargeting" STar" Drive System (Motorized) Recalled by FHC, Inc. Due to...

The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· FHC, Inc.

Recalled Item: microTargeting" Drive System Distributed by Medtronic Recalled by FHC, Inc....

The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· FHC, Inc.

Recalled Item: microTargeting" Drive System Recalled by FHC, Inc. Due to The FHC Depth Stop...

The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· FHC, Inc.

Recalled Item: microTargeting" Lead Adapter for STar" Drive Recalled by FHC, Inc. Due to...

The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· FHC, Inc.

Recalled Item: microTargeting" STar" Drive System (Manual) Distributed by Medtronic...

The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· FHC, Inc.

Recalled Item: microTargeting" Drive System Distributed by Medtronic Recalled by FHC, Inc....

The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· FHC, Inc.

Recalled Item: microTargeting" Lead Adapter for microTargeting" Drive Recalled by FHC, Inc....

The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· FHC, Inc.

Recalled Item: microTargeting" STar" Drive System (Motorized) Distributed by Medtronic...

The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· FHC, Inc.

Recalled Item: microTargeting" Drive System Recalled by FHC, Inc. Due to The FHC Depth Stop...

The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2018· FHC, Inc.

Recalled Item: microtargeting" Depth Stop Adapter Recalled by FHC, Inc. Due to The FHC...

The Issue: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the...

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

Class II — Potential Health HazardOngoing