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. 1,070 recalls have been distributed to Oklahoma in the last 12 months.
Showing 16001–16020 of 49,976 recalls
Recalled Item: Land O Lakes Queso Bravo White Cheese Dip with Jalapeno Recalled by Land...
The Issue: Queso Cheese dip may contain foreign material (metal).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 365 Whole Foods Market Farm Raised Cooked Shrimp 2 lbs/Ready- Recalled by...
The Issue: One lot of uncooked shrimp was inadvertently packaged as cooked shrimp.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Protek Solo Venous Dilator Set: dilator Recalled by Cardiac Assist, Inc Due...
The Issue: On 02/26/2021, it was found that there were incorrectly packaged Dilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System Tray Sysem knee implant devices as follows: Recalled by...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL476...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NO180Z...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL494...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NO156Z...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL470...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Universal Viewer - Product Usage: intended to assist in the...
The Issue: When the Cross Enterprise Display option is enabled on the Centricity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Interventional Fluoroscopic X-Ray System ARTIS icono biplane- 11327600 ARTIS...
The Issue: Siemens has become aware of a potential issue with software version VE20C....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chromosome X Alpha-Satellite in FITC Spectrum - Product Usage: Analyte...
The Issue: Users may observe additional locus specific signals at 9q34. The device pack...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectrum IQ - Infusion Pump - Product Usage: intended to Recalled by Baxter...
The Issue: Potentially defective component in the AC power adapter which may fail over...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revolution CT Recalled by GE Healthcare, LLC Due to GE Healthcare has become...
The Issue: GE Healthcare has become aware of a potential issue on the Revolution CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL482...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Univation X System knee implant devices as follows: Catalog/Product: NL488...
The Issue: Malfunction- loosening of the implant resulting in a potential revision surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD ChloraPrep Hi-Lite Orange 2% w/v chlorhexidine gluconate (CHG) and...
The Issue: Lack of Assurance of Sterility: Product is being recalled because at labeled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ChloraPrep One-Step 2% w/v chlorhexidine gluconate (CHG) and 70% v/v...
The Issue: Microbial Contamination of Non-Sterile Product.Product is being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ChloraPrep One-Step 2% w/v chlorhexidine gluconate (CHG) and 70% v/v...
The Issue: CGMP Deviations: Product is being recalled because at labeled storage...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ChloraPrep With Tint 2% w/v chlorhexidine gluconate (CHG) and 70% Recalled...
The Issue: CGMP Deviations: Product is being recalled because at labeled storage...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.