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. 2,414 recalls have been distributed to Oklahoma in the last 12 months.
Showing 41861–41880 of 49,976 recalls
Recalled Item: Doctor's Best Red Yeast Rice 1200 Recalled by Doctor's Best, Inc. Due to...
The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis discovered undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bard Peripherally Inserted Central Catheter (PICC) and Dialysis catheter...
The Issue: Potential for inadvertent scalpel stick injury involving the safety scalpel.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sonopet Ultrasonic Surgical System Console Recalled by Stryker Instruments...
The Issue: The firm received complaints regarding insufficient irrigation to the tip of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MK5 NX Controller--Wheelchair controller Recalled by Invacare Corporation...
The Issue: M41 Powered Wheelchairs received through Invacare Service Parts (ISP) have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer SST Tubes (RED/GREY TOP SST TUBE 3.5ML) Part Recalled by...
The Issue: Products were held at improper storage temperature
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer PST Tubes (GOLD TOP PST TUBE 3ml) Part Recalled by Fresenius...
The Issue: Products were held at improper storage temperature
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Citrate Tubes (LIGHT BLUE TOP TUBE 2.7ML)Part number: Recalled...
The Issue: Products were held at improper storage temperature
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer EDTA Tubes (LAVENDER TOP TUBE 2.0ML) Part Number: Recalled by...
The Issue: Products were held at improper storage temperature
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Trace Element Tubes (ROYAL BLUE TOP TUBE 6.0ML) Recalled by...
The Issue: Products were held at improper storage temperature
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Serum Tubes (RED TOP PLAIN TUBE 6.0 ML)Part Recalled by...
The Issue: Products were held at improper storage temperature
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis EMPIRA NC RX PTCA Dilatation Catheter Recalled by Cordis Corporation...
The Issue: The balloon may exhibit resistance to the removal of the balloon cover....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis EMPIRA RX PTCA Dilatation Catheter Recalled by Cordis Corporation Due...
The Issue: The balloon may exhibit resistance to the removal of the balloon cover....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS ADVIA Centaur CP Immunoassay System BNP kit Recalled by Siemens...
The Issue: Complaints of failed calibration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS ADVIA Centaur CP Immunoassay System BNP kit Recalled by Siemens...
The Issue: Complaints of failed calibration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT: product code 882482 Recalled by Philips Medical Systems...
The Issue: Flat Panel Display (FPD) failed to remain securely locked in the deployed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Famotidine for Oral Suspension Recalled by Novel Laboratories, Inc. Due to...
The Issue: Failed Impurity/Degradation Specification; 12-month stability time point
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tolterodine Tartrate Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications; Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Disposable StrykeFlow Tip Recalled by Stryker Endoscopy Due to Internal...
The Issue: Internal review found that six lots of Disposable StrykeFlow Tips were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LP Recalled by Laser Peripherals LLC Due to Mislabeling
The Issue: Laser Peripherals LLC is recalling DBLF-60-2 Bare Laser due to a mislabeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Name: Pasteur Pipets Recalled by ORIGIO, Inc Due to Identification of...
The Issue: Identification of packaging breach of the nylon pouch sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.