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. 1,880 recalls have been distributed to Oklahoma in the last 12 months.
Showing 25761–25780 of 49,976 recalls
Recalled Item: Diazepam Rectal Gel Recalled by Valeant Pharmaceuticals North America LLC...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Product distributed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use...
The Issue: The packaging may not be sealed. If the packaging is compromised in this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use...
The Issue: The packaging may not be sealed. If the packaging is compromised in this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triamterene and Hydrochlorothiazide Tablets Recalled by Mylan...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sorin Platinium CRT-D 1741 DF-4 Recalled by Sorin CRM SAS Due to Hardware...
The Issue: Hardware configuration may lead to overconsumption, followed by loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ChloraPrep With Tint Recalled by Merit Medical Systems, Inc. Due to A...
The Issue: A nonsterile bulk product designated for further processing in a tray was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sorin Platinium CRT-D 1711 DF-1 Recalled by Sorin CRM SAS Due to Hardware...
The Issue: Hardware configuration may lead to overconsumption, followed by loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UroLift System Number: UL400-4 Tray Contents: UroLift System Recalled by...
The Issue: Upon implant deployment, the Capsular Tab may not be delivered as the needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical portex First Breath Adult Nasal Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical portex First Breath Adult Nasal Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical portex First Breath Nasal Oxygen Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical portex First Breath Adult Nasal Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical portex First Breath Nasal Oxygen Cannula Recalled by Smiths...
The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: alba BOTANICA sport mineral sunscreen (titanium dioxide 7.0% and zinc...
The Issue: Incorrect Product Formulation: wrong sunscreen product in the package.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Admelog Solostar (insulin lispro injection) Recalled by Sanofi-Aventis U.S....
The Issue: Temperature Abuse: Product samples of Admelog may not have been shipped at...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluocinolone Acetonide Topical Solution Recalled by Teva Pharmaceuticals USA...
The Issue: Failed Impurities and Degradation Specifications and Subpotent Drug:...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Monsel's Solution (Ferric Subsulfate) Recalled by Medgyn Products, Inc. Due...
The Issue: CGMP Deviations: The manufacturer of this product recalled because they were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PINK LEMONADE COOKIES Byrd's FAMOUS COOKIES Recalled by Byrd Cookie Co Due...
The Issue: Red 40 & Red 3 were not listed in the ingredients statement
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PLUS 30 PRIORITY PACK Accessory Kit Product Usage: Is recommended Recalled...
The Issue: Incorrect expiration being entered for one lot.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL800 analyzer Recalled by Radiometer America Inc Due to The analyzer...
The Issue: The analyzer software may cause a mis-match of patient demographics and test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.