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. 936 recalls have been distributed to Oklahoma in the last 12 months.
Showing 44781–44800 of 49,976 recalls
Recalled Item: NexGen CR-Flex Mobile Bearing Tibial Component 9 (Not distributed in...
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Versys¿ Beaded Fullcoat Femoral Stem (POR FULL-CT FEM ST 11X160MM Recalled...
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydrocodone Bitartrate and Acetaminophen Tablets Recalled by Watson...
The Issue: Defective Container: Defective bottles may not have tamper evident seals...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aminosyn II Recalled by Hospira Inc. Due to Presence of Particulate Matter:...
The Issue: Presence of Particulate Matter: Confirmed customer complaint of particulate...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SPIRIVA HandiHaler (Tiotropium Bromide Inhalation Powder) Capsules 18 mcg...
The Issue: Presence of Foreign Substance: This recall is being conducted due to the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IBU (TM) IBUPROFEN Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Labeling: Incorrect or missing lot and/or exp date- This product is being...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cubicin (daptomycin for injection) Recalled by Cubist Pharmaceuticals, Inc....
The Issue: Presence of Particulate Matter; Glass particulates observed in vials
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% Lidocaine HCl and 7.5% Dextrose Injection Recalled by Hospira Inc. Due to...
The Issue: Presence of Particulate Matter; report of visible particulates in the glass...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vicks NyQuil Cold and Flu Nighttime Relief Recalled by Procter & Gamble Co...
The Issue: Incorrect/ Undeclared Excipients: NyQuil Liquid Original bottles were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DePuy Mitek FMS Outflow Tubing with One-Way valve Product Code:284649...
The Issue: Pillow valve included in the FMS Duo outflow tubing set and the FMS Solo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific COGNIS CRT-D Recalled by Boston Scientific CRM Corp Due to...
The Issue: The performance of a low voltage capacitor in a subset of COGNIS CRT-Ds and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific TELIGEN Recalled by Boston Scientific CRM Corp Due to The...
The Issue: The performance of a low voltage capacitor in a subset of COGNIS CRT-Ds and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Combiset Blood Line Hemodialysis use Catalog Number: 03-2622-3. Intended for...
The Issue: Updated Instructions for Use: Bloodline connections not tightened per...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reliance Endoscope Processing System (REPS) Recalled by Steris Corporation...
The Issue: The air pipe that delivers unfiltered ambient air from the procedure room...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008K@ Home Blood lines Combiset True Flow Series for Hemodialysis Recalled...
The Issue: Updated Instructions for Use: Bloodline connections not tightened per...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX- Revolution Recalled by Carestream Health Inc. Due to Carestream Health...
The Issue: Carestream Health Inc. has conducted a voluntary field action which includes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESTREAM DRX -Mobile Retrofit Kit Recalled by Carestream Health Inc. Due...
The Issue: Carestream Health Inc. has conducted a voluntary field action which includes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Combiset Blood Line with BVM for Hemodialysis use Catalog Number: Recalled...
The Issue: Updated Instructions for Use: Bloodline connections not tightened per...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestream DRX-Revolution Mobile X-Ray System -- Made in U.S.A. by Recalled...
The Issue: It was discovered that Carestream received a report from a customer that 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Consult Diagnostics¿ Eon Calcium Reagent For In-Vitro Diagnostic Use PN:...
The Issue: High positive calcium bias on plasma sample versus results on serum
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.