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 31721–31740 of 49,976 recalls
Recalled Item: Sermorelin Acetate 6 mg. Compounded by Tri-Coast Pharmacy Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Quad Mix Recalled by Tri-Coast Pharmacy Due to Lack of Assurance of Sterility
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glutathione 200 mg/mL (30 ML). Compounded by Tri-Coast Pharmacy Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Quad Mix Recalled by Tri-Coast Pharmacy Due to Lack of Assurance of Sterility
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BiMix Phentolamine/Papaverine 1 mg/30 mg/mL (1 ML). Compounded by Tri-Coast...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ultra Amino Energy Cocktail (Methionine (L) 12.5mg/Inositol 25mg/Choline...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: UltraSeal XT Plus Clear . The package contains 4x 1.2 Recalled by Ultradent...
The Issue: There was a labeling error with product, UltraSeal XT Plus Clear , Part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco TRP System The Monaco system is used to make Recalled by Elekta, Inc....
The Issue: Contours are not handled correctly if the CT dataset contains slices with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chocolate Sea Salt Probiotic Granola Recalled by purely elizabeth. Due to...
The Issue: Chocolate Sea Salt Probiotic Granola due to undeclared soy lecithin.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HARVEST SNAPS Recalled by Calbee North America, LLC Due to One lot of black...
The Issue: One lot of black pepper flavored green pea crisps may contain wasabi ranch...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: (R) DEAD BLOW MALLET Recalled by Smith & Nephew, Inc. Due to The firm...
The Issue: The firm received complaints of cracks in the weld on the head of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affinity Fusion" Oxygenator with Integrated Arterial Filter Recalled by...
The Issue: Medtronic is initiating a voluntary product recall for specific lot numbers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Weck Facial Closure Systems have application in laparoscopic procedures for...
The Issue: The devices wings may become partially detached from the EFx Shield during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LightMix¿ Zika rRT-PCR Test The LightMix¿ Zika rRT-PCR Test is Recalled by...
The Issue: The LightCycler¿ 480 algorithm used for the LightMix¿ Zika rRT-PCR Test, EUA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition AS System Recalled by Siemens Medical Solutions USA, Inc...
The Issue: Software update that provides software and firmware bug-fixes to improve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Edge System Recalled by Siemens Medical Solutions USA,...
The Issue: Software update that provides software and firmware bug-fixes to improve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Empowr Knee System Product Usage: Non-porous proximal tibial baseplate...
The Issue: A size 4 Empowr baseplate was mislabeled as a size 6. The affected lot was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular Necks: The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems...
The Issue: All lots of modular neck hip prostheses are being recalled due to a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular REDAPT(TM) Hip Systems The Modular SMF(TM) and Modular REDAPT(TM)...
The Issue: All lots of modular neck hip prostheses are being recalled due to a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Modular SMF(TM) The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems...
The Issue: All lots of modular neck hip prostheses are being recalled due to a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.