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 24021–24040 of 49,976 recalls
Recalled Item: (1) Argon Medical Devices Vascuclamp Recalled by Argon Medical Devices, Inc...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices TRI-JECT Recalled by Argon Medical Devices, Inc Due to...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Argon Medical Devices Double Female LL Adapter Recalled by Argon Medical...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices Double Male LL Adapter Recalled by Argon Medical...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices AHD Luer Lock Cap Recalled by Argon Medical Devices,...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices Hemostasis Valve Recalled by Argon Medical Devices,...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices Septishield II Recalled by Argon Medical Devices, Inc...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices Plugs Recalled by Argon Medical Devices, Inc Due to...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Argon Medical Devices Stopcocks Recalled by Argon Medical Devices, Inc...
The Issue: The seal formed on the edge of the pouch may be incomplete, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MED EL Cochlear Implant System Recalled by MED-EL Elektromedizinische...
The Issue: Devices were distributed despite the Helium-fine leak test results not being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MED EL Cochlear Implant System Recalled by MED-EL Elektromedizinische...
The Issue: Devices were distributed despite the Helium-fine leak test results not being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MED EL Cochlear Implant System Recalled by MED-EL Elektromedizinische...
The Issue: Devices were distributed despite the Helium-fine leak test results not being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radrex-i X-Ray System (DRAD-3000E) TFP-4336W (Wireless FPD) Software...
The Issue: software malfunction; It was found when a user performs radiography using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 500 Recalled by Siemens Healthcare Diagnostics, Inc. Due to...
The Issue: Siemens Healthcare Diagnostics has identified an issue with Dimension Vista...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 1500 Recalled by Siemens Healthcare Diagnostics, Inc. Due to...
The Issue: Siemens Healthcare Diagnostics has identified an issue with Dimension Vista...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Family Wellness First Aid Sterile Gauze Pad 3 in x 3 in Recalled by ASO, LLC...
The Issue: Potential that gauze pads may not be fully sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zero Xtreme Dietary Supplement 30-count capsules. By:Zero Xtreme Registro...
The Issue: Marketed Without an Approved NDA/ANDA: Undeclared Sibutramine
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metoprolol Tartrate Injection Recalled by Baxter Healthcare Corporation Due...
The Issue: Failed pH Specifications: Upward shift in the pH of the solution within the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cidofovir injection 375 mg/mL (75 mg/mL) vial Injection Recalled by Heritage...
The Issue: Lack of Assurance of Sterility: complaints received about dried powder on...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Trace Minerals Dietary Supplement Recalled by Mineralife LLC Due to The...
The Issue: The dietary supplement product is potentially contaminated with Pseudomonas...
Recommended Action: Do not consume. Return to store for a refund or discard.