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 1658116600 of 28,654 recalls

Medical DeviceMarch 2, 2018· Beckman Coulter Inc.

Recalled Item: BECKMAN COULTER iChemVELOCITY Recalled by Beckman Coulter Inc. Due to...

The Issue: Beckman Coulter has determined that there is a potential for incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· Draeger Medical, Inc.

Recalled Item: Fabius Tiro M Recalled by Draeger Medical, Inc. Due to The automatic...

The Issue: The automatic ventilation may fail if the position detection of the motor is...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2018· Draeger Medical, Inc.

Recalled Item: Fabius Tiro Recalled by Draeger Medical, Inc. Due to The automatic...

The Issue: The automatic ventilation may fail if the position detection of the motor is...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2018· Draeger Medical, Inc.

Recalled Item: Fabius GS Premium Recalled by Draeger Medical, Inc. Due to The automatic...

The Issue: The automatic ventilation may fail if the position detection of the motor is...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2018· bioMerieux, Inc.

Recalled Item: VIDAS LH Recalled by bioMerieux, Inc. Due to Several complaints were...

The Issue: Several complaints were received for invalid calibration with low calibrator...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2018· Draeger Medical, Inc.

Recalled Item: Fabius MRI Recalled by Draeger Medical, Inc. Due to The automatic...

The Issue: The automatic ventilation may fail if the position detection of the motor is...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 28, 2018· Vygon U.S.A.

Recalled Item: PICC Insertion Tray Recalled by Vygon U.S.A. Due to Potential friction holes...

The Issue: Potential friction holes may affect the sterility of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2018· Vygon U.S.A.

Recalled Item: PICC Tray Recalled by Vygon U.S.A. Due to Potential friction holes may...

The Issue: Potential friction holes may affect the sterility of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2018· Vygon U.S.A.

Recalled Item: Neonatal PICC Tray Recalled by Vygon U.S.A. Due to Potential friction holes...

The Issue: Potential friction holes may affect the sterility of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2018· Vygon U.S.A.

Recalled Item: PICC Insertion Tray Recalled by Vygon U.S.A. Due to Potential friction holes...

The Issue: Potential friction holes may affect the sterility of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2018· Biomet, Inc.

Recalled Item: Zimmer Biomet Comprehensive Segmental Revision System (SRS). Orthopedic...

The Issue: During assembly, an SRS Humeral Distal Body implant failed to engage...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2018· Vygon U.S.A.

Recalled Item: PICC Kit Recalled by Vygon U.S.A. Due to Potential friction holes may affect...

The Issue: Potential friction holes may affect the sterility of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2018· Vygon U.S.A.

Recalled Item: Maximum Barrier Tray Recalled by Vygon U.S.A. Due to Potential friction...

The Issue: Potential friction holes may affect the sterility of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2018· Vygon U.S.A.

Recalled Item: Maximum Barrier Tray Recalled by Vygon U.S.A. Due to Potential friction...

The Issue: Potential friction holes may affect the sterility of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2018· Vygon U.S.A.

Recalled Item: Maximum Barrier Insertion Tray Recalled by Vygon U.S.A. Due to Potential...

The Issue: Potential friction holes may affect the sterility of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2018· C.R. Bard, Inc.

Recalled Item: Bard(R) Infant Feeding Tube Recalled by C.R. Bard, Inc. Due to BMD has...

The Issue: BMD has identified that the product code/lot number combination identified...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2018· Radiometer Medical ApS

Recalled Item: AQURE Recalled by Radiometer Medical ApS Due to There is a potential problem...

The Issue: There is a potential problem relating to the AQURE System, versions 2.3.0...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2018· C.R. Bard, Inc.

Recalled Item: Bard(R) Adult/Pediatric Feeding Tube Recalled by C.R. Bard, Inc. Due to BMD...

The Issue: BMD has identified that the product code/lot number combination identified...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2018· C.R. Bard, Inc.

Recalled Item: Bard(R) Premature Infant Feeding tube Recalled by C.R. Bard, Inc. Due to BMD...

The Issue: BMD has identified that the product code/lot number combination identified...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2018· C.R. Bard, Inc.

Recalled Item: Bard(R) Premature Infant Feeding Tube Recalled by C.R. Bard, Inc. Due to BMD...

The Issue: BMD has identified that the product code/lot number combination identified...

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

Class II — Potential Health HazardOngoing