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. 2,610 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,610 in last 12 months

Showing 1196111980 of 28,654 recalls

Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· Ivoclar Vivadent AG

Recalled Item: Ivoclar Vivadent IPS e.max ZirCAD CER/inLab Start.Kit LT - ceramic Recalled...

The Issue: Restorations crack during the sintering process.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· Ivoclar Vivadent AG

Recalled Item: Ivoclar Vivadent IPS e.max ZirCAD CER/inLab LT A2 C17/5 - Recalled by...

The Issue: Restorations crack during the sintering process.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· Ivoclar Vivadent AG

Recalled Item: Ivoclar Vivadent IPS e.max ZirCAD CER/inLab LT A3 C17/5 - ceramic for dental...

The Issue: Restorations crack during the sintering process.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· Ivoclar Vivadent AG

Recalled Item: Ivoclar Vivadent IPS e.max ZirCAD CER/inLab LT A1 C17/5 -ceramic for dental...

The Issue: Restorations crack during the sintering process.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2020· Philips North America, LLC

Recalled Item: HeartStart MRx Processor Board PCA Replacement Kits 453563478461 Recalled by...

The Issue: Damaged ESD bags used for storing components in Processor PCA Replacement Kits

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2020· Philips North America, LLC

Recalled Item: Philips Zenition 70 Recalled by Philips North America, LLC Due to When...

The Issue: When strain relief is lost at the stand side of the Stand MVS Trolley Cable,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2020· Philips North America, LLC

Recalled Item: Philips Zenition 50 Recalled by Philips North America, LLC Due to When...

The Issue: When strain relief is lost at the stand side of the Stand MVS Trolley Cable,...

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

Class II — Potential Health HazardOngoing