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. 2,664 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
2,664 in last 12 months

Showing 36213640 of 28,654 recalls

Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MDBNK TWR MN CR-4HH-5FM-P RxNow Recalled by CareFusion 303, Inc....

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-8HH-3FM-P Recalled by CareFusion 303, Inc. Due to...

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-2HH-6FH Recalled by CareFusion 303, Inc. Due to...

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-8HH-2FH-1FM-P Recalled by CareFusion 303, Inc....

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-4HH-1FH-4FM-P Recalled by CareFusion 303, Inc....

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK MINI CR-2HH-1FH-P Recalled by CareFusion 303, Inc. Due to...

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-6HH-1FH-3FM-P Recalled by CareFusion 303, Inc....

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-8HH-3FH-P Recalled by CareFusion 303, Inc. Due to...

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-12HH-1FH Recalled by CareFusion 303, Inc. Due to...

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-12HH-1FM-P Recalled by CareFusion 303, Inc. Due...

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-8HH-1FH-2FM-P Recalled by CareFusion 303, Inc....

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-10HH-2FM-P Recalled by CareFusion 303, Inc. Due...

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-4HH-5FM-P Recalled by CareFusion 303, Inc. Due to...

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-14HH-P Recalled by CareFusion 303, Inc. Due to...

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-10HH-2FH-P Recalled by CareFusion 303, Inc. Due...

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK TWR MN CR-2HH-6FM Recalled by CareFusion 303, Inc. Due to...

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2024· CareFusion 303, Inc.

Recalled Item: BD PYXIS MEDBANK MINI CR-4HH-P Recalled by CareFusion 303, Inc. Due to Due...

The Issue: Due to software issue, there is a potential when a restock label is printed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2024· Olympus Corporation of the Americas

Recalled Item: ESG-410 Electrosurgical Generator- In conjunction with electrosurgical...

The Issue: Electrosurgical Generators ESG-410 does not power on upon use, may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2024· Cepheid

Recalled Item: Cepheid Recalled by Cepheid Due to Specimen collection device may leak after...

The Issue: Specimen collection device may leak after the patient sample swabs have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2024· Luminex Corporation

Recalled Item: Verigene Gram Positive Blood Culture (BC-GP) Nucleic Acid Test Recalled by...

The Issue: Potential for defective test cartridges which may result in false positive...

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

Class II — Potential Health HazardOngoing