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. 2,576 recalls have been distributed to Oklahoma in the last 12 months.
Showing 16441–16460 of 49,976 recalls
Recalled Item: Grasper/Retriever Recalled by Shent USA, Inc. Due to Mislabeling
The Issue: Mislabeled: Devices labeled as catalog #7208 (Grasper/Retriever, Alligator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Natus Manufacturing Limited Due to The external drainage system...
The Issue: The external drainage system failed to meet Pyrogen test requirements for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Testosterone Cypionate Injection Recalled by SUN PHARMACEUTICAL INDUSTRIES...
The Issue: Incorrect Labeling: Incorrect lot number on secondary packaging
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bard Clean-Cath Intermittent Catheter Recalled by C.R. Bard, Inc. Due to The...
The Issue: The device catheter tip was cut off (no tip) and the product packaging was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slush + Warmer Disc Drape Recalled by Ecolab Inc Due to Slits were...
The Issue: Slits were identified in a low quantity of ORS-320 Slush + Warmer Disc...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Cerebro Spinal Fluid Flow Control Valves and Shunts. STRATA...
The Issue: Potential for variation in radiopaque marking visibility under radiographic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic PS Medical Cerebro Spinal Fluid (CSF)-Flow Control Valves for...
The Issue: Potential for variation in radiopaque marking visibility under radiographic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Delta CSF (Cerebro Spinal Fluid) -Flow Control Valves for Recalled...
The Issue: Potential for variation in radiopaque marking visibility under radiographic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nortriptyline HCl Capsules Recalled by Taro Pharmaceuticals U.S.A., Inc. Due...
The Issue: CGMP deviations.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: JTM FOOD GROUP brand READY TO EAT WHITE CHEDDAR MACARONI Recalled by JTM...
The Issue: Possible metal shavings.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: WMTS Telemetry Receiver Recalled by Nihon Kohden America Inc Due to...
The Issue: Incorrect Date Stamp or No Data Transfer on Telemetry Receiver and Transmitter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 13C-Spirulina Gastric Emptying Breath Test (GEBT) - Product Usage: intended...
The Issue: Potential for false negative diagnosis of gastroparesis. Certain GEBT kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Femoral Sleeves - Product Usage: used primarily in revision...
The Issue: The taper dimensions may be out of specification due to a production issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phytonadione Tablets 5mg Recalled by Bausch Health Companies, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications:Out of specification during the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mephyton (phytonadione) Tablets 5mg Recalled by Bausch Health Companies,...
The Issue: Failed Impurities/Degradation Specifications:Out of specification during the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nitrofurantoin Capsules USP (Monohydrate/Macrocrystals) Recalled by American...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The PrisMax System Version II Hemodialysis Delivery System: Automatic...
The Issue: Variability in the performance of the tubing in the ARPS (Automatic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lab Coats SMS X-Large Blue Recalled by Cardinal Health 200, LLC Due to...
The Issue: There is a potential for rips, holes, tears, incomplete and/or open seams,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kendall Spill Kit Recalled by Cardinal Health 200, LLC Due to Foreign Object...
The Issue: Gowns included in the kits potentially have rips, holes, tears, incomplete...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gown Isolation W/Ties Xl Blue Recalled by Cardinal Health 200, LLC Due to...
The Issue: There is a potential for rips, holes, tears, incomplete and/or open seams,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.