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. 2,580 recalls have been distributed to Oklahoma in the last 12 months.
Showing 15741–15760 of 49,976 recalls
Recalled Item: Flurandrenolide Ointment USP Recalled by Teligent Pharma, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PERLA TL Lateral Connector Open - Product Usage: intended to Recalled by...
The Issue: Due to external labelling error/mix-up. Affected product external labels...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FISTULA ON-OFF KIT. Medical convenience kit Recalled by Avid Medical, Inc....
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DIALYSIS ACCESS Medical convenience kit Recalled by Avid Medical, Inc. Due...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COVID-19 Self-Test Kit *** INNOVA *** 3T Recalled by INNOVA MEDICAL GROUP,...
The Issue: Due to distributing test kits to customers who were not part of a clinical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: For In Vitro Diagnostic Use Only *** 25T 888 SARS-CoV-2 Recalled by INNOVA...
The Issue: Due to distributing test kits to customers who were not part of a clinical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADULT CHEST TUBE TRAY. Medical convenience kit Recalled by Avid Medical,...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FISTULA (ON/OFF) ALL IN ONE BAG. Medical convenience kit Recalled by Avid...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COVID-19 Self-Test Kit *** INNOVA *** 7T Recalled by INNOVA MEDICAL GROUP,...
The Issue: Due to distributing test kits to customers who were not part of a clinical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit: LVAD Dres Chg. MAI Kit Part Number: 79544B Recalled by Medical Action...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit: CentralLineDresChangeClrSeq MAI Kit Part Number: 79420 Recalled by...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit: Blood Culture. MAI Kit Part Number: 80315D Recalled by Medical Action...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit: Midline Insertion DA. MAI Kit Part Number: 77981B Recalled by Medical...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit: Injection REVIEW MAI Kit Part Number: 74736 Recalled by Medical Action...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit: Blood Culture MAI Kit Part Number: 80076 Recalled by Medical Action...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
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.
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.
Recalled Item: Angio Pack Recalled by Windstone Medical Packaging, Inc. Due to Angio tubing...
The Issue: Angio tubing included within Custom Convenience kits may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Angio Pack Recalled by Windstone Medical Packaging, Inc. Due to Angio tubing...
The Issue: Angio tubing included within Custom Convenience kits may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.