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. 2,576 recalls have been distributed to Oklahoma in the last 12 months.
Showing 16601–16620 of 49,976 recalls
Recalled Item: Relieva PF Preservative-Free Lubricant Eye Drops 0.33 fl oz Recalled by...
The Issue: Labeling: Missing instructions for use insert
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ACCESS SARS-CoV-2 IgG QC SARS-CoV-2 IgG - Product Recalled by Beckman...
The Issue: The Quality Control (QC) card has a label error for the standard deviation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Paroex (Chlorhexidine Gluconate) Oral Rinse Recalled by Sunstar Americas,...
The Issue: cGMP Deviations; FDA inspection of manufacturing facility observed potential...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levetiracetam Oral Solution Recalled by Akorn, Inc. Due to Defective...
The Issue: Defective container: Customer complaints for oral solution leaking from bottles.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tourni-Cot - Universal Recalled by Mar-Med Co Due to A failure can occur if...
The Issue: A failure can occur if the user attempts to remove the device by partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLOW COUPLER Monitor Flow Coupler devices are sold in 5 sizes (2.0 mm...
The Issue: Potential for the battery to lose its ability to be recharged.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHILIPS Incisive Computed tomography X-ray system Incisive CT Software...
The Issue: Patient tabletop moved out to the home position during scan initialization,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips EPIQ Diagnostic Ultrasound System Recalled by Philips Ultrasound Inc...
The Issue: Control panel arm assembly could have missing or loose screws where undue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMC Wash-Free Hand Sanitizer Recalled by Shane Erickson Inc Due to CGMP...
The Issue: CGMP Deviations: product manufactured at the same facility that produced...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IMC Wash-Free Hand Sanitizer Recalled by Shane Erickson Inc Due to CGMP...
The Issue: CGMP Deviations: product manufactured at the same facility that produced...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IMC Wash-Free Hand Sanitizer Recalled by Shane Erickson Inc Due to CGMP...
The Issue: CGMP Deviations: product manufactured at the same facility that produced...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketorolac Tromethamine Injection Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Presence of Particulate Matter - found in reserve sample vials at the firm.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxycodone Hydrochloride Oral Solution Recalled by Genus Lifesciences Inc....
The Issue: Presence of Foreign Substance: Particulate matter was found in multiple lots...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fresh Whole Blood Donor Set (P/N 80-801-D NSN 6515016640306) . Recalled by...
The Issue: There is the potential of a bent or disconnected needle in one of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Valkyrie LTOWB Collection (P/N 80-820 Recalled by Combat Medical Systems,...
The Issue: There is the potential of a bent or disconnected needle in one of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresh Whole Blood Transfusion Set (P/N 80-801 NSN 6515016574750) . Recalled...
The Issue: There is the potential of a bent or disconnected needle in one of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Valkyrie LTOWB Administration (P/N 80-821 NSN 6515016862401). Blood...
The Issue: There is the potential of a bent or disconnected needle in one of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Low Titer Type O FWB Transfusion Set (P/N 80-875 NSN Recalled by Combat...
The Issue: There is the potential of a bent or disconnected needle in one of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Hypodermic Syringe 10 ml Recalled by Becton Dickinson & Company Due to...
The Issue: The product packaging for the 10 ml eccentric tip syringe may exhibit open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity Acute Care System (IACS) Monitoring Solution: The IACS is Recalled...
The Issue: The Infinity M540 patient monitor may randomly reboot due to an error to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.