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. 1,030 recalls have been distributed to Oklahoma in the last 12 months.
Showing 20521–20540 of 49,976 recalls
Recalled Item: LAG SCREW 3.2MM GUIDE PIN SLEEVE Recalled by Smith & Nephew, Inc. Due to LAG...
The Issue: LAG SCREW 3.2 GUIDE PIN SLEEVE are being recalled due to a manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software versions syngo CT VB20 running on the following Siemens Recalled by...
The Issue: Software issue identified in the software versions syngo CT VB20 running on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxymetry Cable Recalled by Edwards Lifesciences, LLC Due to Intermittent...
The Issue: Intermittent communication due to inconsistent crimping of connectors onto...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Legacy 3 Implant Recalled by Implant Direct Sybron Manufacturing LLC Due to...
The Issue: Some dental implant packages contain incorrect implants, which could lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Star 8 Rolling Walker/Rollator Recalled by Nova Ortho-Med Inc Due to Walkers...
The Issue: Walkers within the identified serial range have the potential for the front...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rifampin for Injection Recalled by Mylan Laboratories Limited (Sterile...
The Issue: Failed Impurities/Degradation Specifications: discoloration due to elevated...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dole Crushed Pineapple in 100% pineapple juice Manufactured For Dole...
The Issue: Foreign object; potential plastic pieces.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...
The Issue: Communication error alarms may result in interruption of therapy, delay in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...
The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...
The Issue: Communication error alarms may result in interruption of therapy, delay in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche Homocysteine-In vitro test for the quantitative determination of total...
The Issue: Homocysteine Reagent, Calibration Failures and Quality Control Recovery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WECK Hem-O-Lok AutoEndo5 Recalled by Teleflex Medical Due to Certain clip...
The Issue: Certain clip appliers have an increase in misloading and/or jamming related...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 111" 10 Drop Admin Set w/2 Inj Sites Recalled by ICU Medical, Inc. Due to...
The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...
The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...
The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neocis Guidance System Fiducial Array - Product Usage: The Neocis Recalled...
The Issue: The Fiducial Array may mismatch their measurement files resulting in failed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...
The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex Control Unit Recalled by Baxter Healthcare Corporation Due to...
The Issue: Communication error alarms may result in interruption of therapy, delay in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...
The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by ICU Medical, Inc. Due to There is a potential that IV...
The Issue: There is a potential that IV administration sets contain a 15 drops/mL drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.