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. 2,468 recalls have been distributed to Oklahoma in the last 12 months.
Showing 31121–31140 of 49,976 recalls
Recalled Item: Daavlin Aquex (DAAV1000) Recalled by Hidrex GmbH Due to The device was...
The Issue: The device was reclassified from a class III device to a class II device and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hidrex USA DP450 Recalled by Hidrex GmbH Due to The device was reclassified...
The Issue: The device was reclassified from a class III device to a class II device and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LipiFlow Thermal Pulsation System/LipiFlow Recalled by Tearscience, Inc Due...
The Issue: Labeling: The labeled storage temperature is not consistent with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hidrex USA DVP1000 Recalled by Hidrex GmbH Due to The device was...
The Issue: The device was reclassified from a class III device to a class II device and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tarina Fe 1/20 (Norethindrone Acetate and Ethinyl Estradiol Tablets Recalled...
The Issue: Chemical Contamination: out of specification results for impurities were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glipizide extended-release tablets Recalled by Actavis Inc Due to Failed...
The Issue: Failed Dissolution Specifications. Above out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Norethindrone Acetate and Ethinyl Estradiol Tablets Recalled by Mylan...
The Issue: Chemical Contamination: out of specification results for impurities were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mirtazapine Tablets Recalled by Mylan Institutional, Inc. (d.b.a. UDL...
The Issue: Presence of Foreign Tablets/Capsules; possibility of Glipizide 10 mg tablets...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Buffered Lidocaine Recalled by Pharmedium Services, LLC Due to Labeling;...
The Issue: Labeling; Label Mixup; outer packaging is incorrectly labeled as Buffered...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VASOVIEW HEMOPRO VH-3500 ENDOSCOPIC VESSEL HARVESTING SYSTEM Product Usage:...
The Issue: Maquet has received several complaints involving the VASOVIEW HEMOPRO...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Sodium Polyanetholesulfonate 5.95 mg Sodium Chloride 14.4 mg...
The Issue: After a receiving a customer complaint for incorrect labeling, BD has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Falafel King Tzatziki Sauce. 10 ounce. Plastic container Recalled by Falafel...
The Issue: Falafel King announced a recall for their Tzatziki Sauce due to undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pharmanex ageLOC TR90 Protein Boost. Protein Powder. Net wt. 1.59 Recalled...
The Issue: Nu Skin announces a voluntary field action for Pharmanex ageLOC TR90 Protein...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The ABL800 Model#:All Recalled by Radiometer America Inc Due to Reports that...
The Issue: Reports that the sample type "cord blood" has been changed into the two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL90 Flex Model #: 393-090 Portable Recalled by Radiometer America Inc Due...
The Issue: Reports that the sample type "cord blood" has been changed into the two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Valleylab Laparoscopic Handset Recalled by COVIDIEN MEDTRONIC Due to...
The Issue: Customer reports of the device handset continuing to operate after release...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Influenza Transport Swab Packages Recalled by Quidel Corporation Due to...
The Issue: Quidel Corporation is recalling Influenza Transport Swab Packages because it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVATRON M 7400/7440(MEX) Accelerator Recalled by Siemens Medical Solutions...
The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRIMUS HI and Mevatron M2/Primus Mid-Energy Recalled by Siemens Medical...
The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVATRON M 6700 (MX) Accelerator Recalled by Siemens Medical Solutions USA,...
The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.