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. 1,070 recalls have been distributed to Oklahoma in the last 12 months.

49,976 total recalls
1,070 in last 12 months

Showing 15761–15780 of 49,976 recalls

FoodApril 8, 2021· Natrol, LLC

Recalled Item: Natrol Melatonin 3 mg Recalled by Natrol, LLC Due to One lot of ALA 300 mg...

The Issue: One lot of ALA 300 mg Cap-50 were labeled at Melatonin 3 mg Tab-60.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugApril 8, 2021· NSNY Distributor Inc

Recalled Item: Ginseng Power 5000 capsule Recalled by NSNY Distributor Inc Due to...

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugApril 8, 2021· NSNY Distributor Inc

Recalled Item: Premium OrgaZEN 7000 capsule Recalled by NSNY Distributor Inc Due to...

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....

The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....

The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....

The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....

The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....

The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....

The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....

The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....

The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....

The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....

The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Roche Diagnostics Operations, Inc.

Recalled Item: Elecsys Troponin I Immunoassay: Catalog# 05094810160 - Product Usage:...

The Issue: Recall reason is possible sporadic false negative conventional troponin...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....

The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....

The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....

The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....

The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Bard Access Systems Inc.

Recalled Item: Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1....

The Issue: Catheters contain two issues: 1. the inner diameter of the distal connector...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2021· Roche Diagnostics Operations, Inc.

Recalled Item: Elecsys Troponin I STAT Immunoassay: Catalog# 05094798160 - Product Usage:...

The Issue: Recall reason is possible sporadic false negative conventional troponin...

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

Class II — Potential Health HazardOngoing