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. 2,654 recalls have been distributed to Oklahoma in the last 12 months.
Showing 5641–5660 of 49,976 recalls
Recalled Item: IBA Proton Therapy System - PROTEUS 235 - Designed to Recalled by Ion Beam...
The Issue: Irradiation is not interrupted when some C230 Accelerator Control Unit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syringes with Eccentric Tips labeled as: 1) SOL-M 10ml Eccentric Recalled by...
The Issue: Products in distribution were found by FDA to be to be substantially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syringes with Luer Slip Tips labeled as: 1) SOL-M 1ml Recalled by...
The Issue: Products in distribution were found by FDA to be to be substantially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syringes with Low Dead Space labeled as: a) SOL-M 1ml Recalled by...
The Issue: Products in distribution were found by FDA to be to be substantially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syringes with exchangeable needles labeled as: SOL-CARE: 1) SOL-CARE 10ml...
The Issue: Products in distribution were found by FDA to be to be substantially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syringes with Fixed Needles labeled as: a) SOL-M: 1) SOL-M Recalled by...
The Issue: Products in distribution were found by FDA to be to be substantially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syringe Tip Caps labeled as: 1) SOL-M Syringe Tip Cap Recalled by...
The Issue: Products in distribution were found by FDA to be to be substantially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: First Source Vision M. Portable cart and platform that supports Recalled by...
The Issue: Potential for the bolt that secures the positioning arm to the gas spring to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: First Source iQ Flex M. Portable cart and platform that Recalled by First...
The Issue: Potential for the bolt that secures the positioning arm to the gas spring to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Hoffman LRF Wire Tensioner Recalled by Stryker GmbH Due to The...
The Issue: The adjustment ring on the device may become loose resulting in the wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Medical SureStep Foley Tray System Recalled by C.R. Bard Inc Due to...
The Issue: Some of the devices may function incorrectly resulting in no temperature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Tempus LS-Manual Defibrillator Recalled by Remote Diagnostic...
The Issue: Simultaneous ECG measurements with multiple devices, including a manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cefdinir for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc. Due...
The Issue: Defective container: lack of seal integrity.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Centrella Max - The Centrella Smart+ Bed is intended for Recalled by Baxter...
The Issue: There is a potential for the top cover of the hospital bed mattress to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thoratec HeartMate System Monitor Recalled by Thoratec Corp. Due to System...
The Issue: System monitor screen may display atypical behavior: Overlapping...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. Reusable Patient...
The Issue: Reports of patient burns.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Vitamin B12 Range Verifier - In vitro...
The Issue: The results generated by the VITROS Immunodiagnostic Products Vitamin B12...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drug Vial Label: Zilretta¿ (triamcinolone acetonide extended-release...
The Issue: Failed Stability Specifications - at 12 months 2-8 degrees C followed by 6...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets Recalled by MACLEODS...
The Issue: Presence of foreign substance: plastic-like substance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medline ReNewal Reprocessed Covidien LigaSure Maryland Jaw Sealer/Divider...
The Issue: Potential for an incomplete seal on the packaging tray.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.