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 27221–27240 of 49,976 recalls
Recalled Item: SunGlow Recalled by Ventura Foods Llc Due to Undeclared Soy
The Issue: SunGlow contains undeclared soy lecithin.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Clopidogrel Tablets Recalled by International Laboratories, LLC Due to...
The Issue: LABELING: LABEL MIX-UP. Simvastatin tablets, USP 10 mg were found in bottles...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lovastatin Tablets USP Recalled by AVKARE Inc. Due to Failed Dissolution...
The Issue: Failed Dissolution Specifications: Low out of specification results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brilliance Big Bore Oncology CTwith 4.2.0 software version. Model #'...
The Issue: Software issues including: Software errors that may result in Extended Field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance Big Bore Radiology CT with 4.2.0 software version. Model Recalled...
The Issue: Software issues including: Software errors that may result in Extended Field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MyLab Ultrasound System Recalled by ESAOTE S.P.A. Due to The ultrasound...
The Issue: The ultrasound system used in certain settings may result in overheating of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MyLab Ultrasound System Recalled by ESAOTE S.P.A. Due to The ultrasound...
The Issue: The ultrasound system used in certain settings may result in overheating of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percuvance(R) Percutaneous Shaft 29cm Recalled by Teleflex Medical Due to...
The Issue: There is potential for a piece of the distal tip on the Percuvance shaft to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percuvance(R) Percutaneous Shaft 36cm Recalled by Teleflex Medical Due to...
The Issue: There is potential for a piece of the distal tip on the Percuvance shaft to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chocolate Covered Vanilla Ice Cream Bars packaged under the following...
The Issue: Product may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Orange Cream Ice Cream Bars sold under the following labels: Recalled by...
The Issue: Product may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Frozen Unbaked Biscuits sold under the brand names of Hilltop Hearth...
The Issue: Firm was notified of a positive test result for Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ice Cream Variety Packs containing Sandwiches Recalled by Fieldbrook Foods...
The Issue: Product may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: RASPBERRY Cream Ice Cream Bars: Sundae SHOPPE Recalled by Fieldbrook Foods...
The Issue: Product may be contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dimension Vista¿ Thyroid Stimulating Hormone (TSH) Flex¿ reagent cartridge...
The Issue: The concentrations for biotin listed in the non-interfering substances...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE ¿ 2000/IMMULITE ¿ 2000 XPi BR-MA (CA15-3) Recalled by Siemens...
The Issue: Concentrations for the level of biotin that does not interfere is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE ¿ /IMMULITE 1000 ¿ Gastrin Recalled by Siemens Healthcare...
The Issue: Concentrations for the level of biotin that does not interfere is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE ¿ /IMMULITE ¿ 1000 BR-MA (CA15-3) Recalled by Siemens Healthcare...
The Issue: Concentrations for the level of biotin that does not interfere is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE ¿ /IMMULITE ¿ 1000 OM-MA (CA125) Recalled by Siemens Healthcare...
The Issue: Concentrations for the level of biotin that does not interfere is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur¿ DHEA-SO4 Recalled by Siemens Healthcare Diagnostics, Inc. Due...
The Issue: The concentrations for biotin listed in the non-interfering substances...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.