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 28061–28080 of 49,976 recalls
Recalled Item: Country Harvest brand Black Thunder Bean Soup Recalled by Country Harvest,...
The Issue: Country Harvest brand Black Thunder Bean Soup is recalled because the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Country Harvest brand Lentil Barley Soup Recalled by Country Harvest, Inc....
The Issue: Country Harvest brand Lentil Barley Soup is recalled because the ingredients...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Shawnee Mills Peppered Gravy Mix Recalled by Shawnee Milling Company, Inc....
The Issue: Potential for foreign material in a food product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 14-442000S Antegrade Femoral Nail Instrument Kit Recalled by Zimmer Biomet,...
The Issue: Fracture of the bolt connecting the insertion guide to the intramedullary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 979195 Loaner Kit for femoral intramedullary nail. Orthopedic instrument....
The Issue: Fracture of the bolt connecting the insertion guide to the intramedullary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phoenix Antegrade Femoral Nail Trochanteric and Piriformis fossa Recalled by...
The Issue: Fracture of the bolt connecting the insertion guide to the intramedullary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equate Beauty Clarifying Face Daily Moisturizer 4 fl. oz. (118 Recalled by...
The Issue: Failed Stability Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Procrit (epoetin alfa) Recalled by Amgen, Inc. Due to Presence of...
The Issue: Presence of particulate matter: glass flakes identified as lamellae observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: OTTO BOCK Kenevo knee joints Model 3C60=ST Recalled by Otto Bock Healthcare...
The Issue: Otto Bock Healthcare Products GmbH has identified a design issue through...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim DRG Implantable Pulse Generator Model 3664 Recalled by St. Jude...
The Issue: Analysis of the difference between the actual device longevity and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity 5 Implantable Pulse Generator and Infinity 7 Implantable Pulse...
The Issue: Analysis of the difference between the actual device longevity and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT DE handheld data processing module for clinical use Recalled by...
The Issue: Issues resulting from upgrade to software version 2.8: (1) Location,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeVest Wearable Defibrillator Model 4000 Recalled by Zoll Manufacturing...
The Issue: Incorrect service code for properly catching critical defects during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim 5 Elite Implantable Pulse Generator and Proclaim 7 Elite Recalled...
The Issue: Analysis of the difference between the actual device longevity and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OTTO BOCK Kenevo knee joints Model 3C60 Recalled by Otto Bock Healthcare...
The Issue: Otto Bock Healthcare Products GmbH has identified a design issue through...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba Medical Kalare Fluoroscopic X-Ray System (DREX-KL80) Kalare is...
The Issue: During an examination images were displayed on the live monitor,but the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sysmex Fluorocell(R) PLT Fluorocell PLT is used to stain platelets Recalled...
The Issue: There is potential that fluorescent platelet (PLT-F) and immature platelet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AutoCheck5+ Recalled by Radiometer America Inc Due to Radiometer has...
The Issue: Radiometer has recently become aware that a few of the AUTOCHECK 5+ level 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Garden of Life Recalled by Garden Of Life, LLC Due to The product may pose a...
The Issue: The product may pose a choking hazard to newborns due to the thickness of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Organic Coconut Sugar Recalled by NOW Foods Due to Undeclared Gluten
The Issue: Undeclared gluten found in the product and the product is labeled "Gluten Free".
Recommended Action: Do not consume. Return to store for a refund or discard.