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. 2,485 recalls have been distributed to Oklahoma in the last 12 months.
Showing 21981–22000 of 28,654 recalls
Recalled Item: Voyant Open Fusion Device Models: EB040 and EB040+ Product Usage: Recalled...
The Issue: Potential to improperly characterize tissue within the jaws, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Pressure Monitoring Kit with TruWave disposable pressure transducer....
The Issue: Flow restriction issues in a trifurcated IV set included in the pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AU480 Chemistry Analyzers Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman coulter has received complaints regarding leaking and cracked C...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AU680 Chemistry Analyzers Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman coulter has received complaints regarding leaking and cracked C...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PICC Kits with Peel-Away Sheath Component Recalled by Arrow International...
The Issue: the catheter peel-away component hub tabs may prematurely detach. One injury...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AU5800 Chemistry Analyzers Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman coulter has received complaints regarding leaking and cracked C...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow International Recalled by Arrow International Inc Due to saline...
The Issue: saline leakage from unsecured connections between the Touhy Borst adaptor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaPlus Trach Care* Closed Suction System for Adults Recalled by Halyard...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Wet Pak* Closed Suction System for Adults Recalled by Halyard...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Multi-Access Port Replacement Catheter for Adults Recalled by...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaPlus Trach Care* Closed Suction System for Adults Recalled by Halyard...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Multi-Access Port Closed Suction System for Adults Recalled by...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Multi-Access Port Replacement Catheter for Adults Recalled by...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Sciatic Nerve Retractor and Sciatic Nerve Retractor Long Recalled by...
The Issue: Potential for micropores to form, allowing fluid to enter the hollow handle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VEPTR Vertical Expandable Prosthetic Titanium Rib Recalled by Synthes (USA)...
The Issue: The last hole on certain VEPTR Inferior Cradles may be partially formed....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent* Closed Suction System for Adults Recalled by Halyard Health, Inc...
The Issue: The thumb valve of some KIMVENT Closed Suction Systems remained partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.