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. 2,509 recalls have been distributed to Oklahoma in the last 12 months.
Showing 22901–22920 of 49,976 recalls
Recalled Item: Trimix HIGH (Papaverine HCl 30 mg/mL Phentolamine Mesylate 2 mg/mL Recalled...
The Issue: Lack of assurance of sterility for injectables and solutions intended to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BPlex (METHYLCOBALAMIN 1000 MCG/ML PYRIDOXAL 5 PHOSPHATE 20MG/ML...
The Issue: Lack of assurance of sterility for injectables and solutions intended to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Test D (TESTOSTERONE CYPIONATE 200MG/ML VITAMIN D3 5 Recalled by...
The Issue: Lack of assurance of sterility for injectables and solutions intended to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lipoplex (METHIONINE 25 MG/ML INOSITOL 50 MG/ML CHOLINE CHLORIDE 50 Recalled...
The Issue: Lack of assurance of sterility for injectables and solutions intended to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GlipiZIDE Extended-release Tablets Recalled by American Health Packaging Due...
The Issue: Failed Dissolution Specifications: dissolution failure at time zero of the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glutathione 200mg/mL inj. a) 10 ML and b) 12 ML Recalled by Customceutical...
The Issue: Lack of assurance of sterility for injectables and solutions intended to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HCG (CHORIONIC GONADOTROPIN 1000 IU/ML PEP 25 mg/mL) inj 5 Recalled by...
The Issue: Lack of assurance of sterility for injectables and solutions intended to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Test D (TESTOSTERONE CYPIONATE 200MG/ML VITAMIN D3 5 Recalled by...
The Issue: Lack of assurance of sterility for injectables and solutions intended to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kopi Jantan Tradisional Natural Herbs Coffee Recalled by Brian P. Richardson...
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cashew Brittle Bits in clear 4oz bag with a Best Recalled by Hercules Candy...
The Issue: Product may contain undeclared peanuts
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Alinity i Processing Module Recalled by Abbott Gmbh & Co. KG Due to...
The Issue: Potential loose cable connections on the reagent cooler, which could result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SoundWave Professional Suite Software 3.2 Recalled by Advanced Bionics, LLC...
The Issue: The manufacturer received complaints that customers were attempting to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas p 501 post-analytical units Recalled by Roche Diagnostics Corporation...
The Issue: There is a potential for the tray input flap on the post analytical units to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas p 701 post-analytical units Recalled by Roche Diagnostics Corporation...
The Issue: There is a potential for the tray input flap on the post analytical units to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T BlueStar Machine Software v.2.72-Hemodialysis machine Model Number:...
The Issue: Power Logic Board Fail Message on the 2008T BlueStar Machine with software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Veritor System Reader -In Vitro Diagnostic for use with Recalled by...
The Issue: Background calibration has the potential to cause false positive or false...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adapter for handpiece Recalled by Thommen Medical AG Due to Dental adaptor...
The Issue: Dental adaptor does not conform to specifications. The dental coupling of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Veritor Plus Analyzer- In-Vitro Diagnostic intended to use with Recalled...
The Issue: Background calibration has the potential to cause false positive or false...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Autoimmune EIA Anti-Tissue Transglutaminase (tTG) IgA Test Recalled by...
The Issue: An elevated lot-to-lot bias was observed for Autoimmune EIA Anti-Tissue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta Unity systems Product Usage: Elekta Unity using Magnetic Resonance...
The Issue: There is no warning in the Elekta Unity manual for the administration of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.