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. 2,580 recalls have been distributed to Oklahoma in the last 12 months.
Showing 15861–15880 of 49,976 recalls
Recalled Item: Tuscan Garden Ranch Dressing Recalled by Richelieu Foods, Inc. Due to An...
The Issue: An incorrect label was applied to the back of ranch dressing bottles. The...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: NPr FCZ¿Imp Crwn ASC CC RP CAD 1-25¿ s4 - Recalled by Nobel Biocare Procera...
The Issue: Not manufactured to specification
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NPr FCZ¿Imp Crwn ASC CC NP CAD 1-25¿ s4 - Recalled by Nobel Biocare Procera...
The Issue: Not manufactured to specification
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NPr FCZ¿Imp Crwn ASC CC RP CAD 1-25¿s3 - Product Recalled by Nobel Biocare...
The Issue: Not manufactured to specification
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NPr FCZ¿Imp Crwn ASC CC NP CAD 1-25¿ s6 - Recalled by Nobel Biocare Procera...
The Issue: Not manufactured to specification
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NPr FCZ¿Imp Crwn ASC CC RP CAD 1-25¿ s2 - Recalled by Nobel Biocare Procera...
The Issue: Not manufactured to specification
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Provox Life Night HME Recalled by Atos Medical AB Due to Provox Life Night...
The Issue: Provox Life Night HME may be incorrectly inserted sideways or forcefully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AFT Straight Tube (3/4 Filled) - Human Allograph Tissue for Recalled by...
The Issue: 3/4 AFT Straight Fill Tubes (227007) filled only 1/2 way instead of 3/4, may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUETTE¿ Blood Collection tube 9NC Coagulation sodium citrate 3.2% 13x75...
The Issue: VACUETTE¿ Blood Collection tube 9NC Coagulation sodium citrate 3.2% may show...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Xper Flex Cardio (FC2010 Recalled by Philips North America Llc Due...
The Issue: Performance issues with the Xper Flex Cardio Physio Monitoring System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thumbs Up 7 Red 70K Recalled by Antoto-K Due to Marketed without Approved...
The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cefprozil for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc. Due...
The Issue: Superpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PIC070 Arterial Blood Sampler PICO70 - Product Usage: Preheparinized...
The Issue: Radiometer has become aware of an issue with PICO70 Arterial Blood Sampler....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Regard Dressing Change Tray Recalled by ROi CPS LLC Due to ChloraPrep...
The Issue: ChloraPrep applicators in the kit can grow organisms that can result in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ Black Slides CATALOG #: J02316 - Product Usage: Recalled by...
The Issue: Delayed results. Ortho confirmed that two lots of VITROS Black Slides are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee ceiling-interventional Fluoroscopic X-Ray System Model Number:...
The Issue: Some Artis zee ceiling systems show an increased abrasion of the cabling at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Imperial Extreme 2000 Capsules Recalled by S & B Story LLC Due to Marketed...
The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PremierZen Black 5000 capsules Recalled by Namoo Enterprise LLC Due to...
The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metformin HCl Extended-Release Tablets Recalled by SUN PHARMACEUTICAL...
The Issue: Failed Moisture Limits: Out of specification for water content
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mometasone Furoate Topical Solution Recalled by Cosette Pharmaceuticals,...
The Issue: CGMP Deviaitons
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.