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 21961–21980 of 28,654 recalls
Recalled Item: Monoject 0.9% Saline Flush Prefill Double Pouch Item Code: 8881570129...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled by...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mahurkar Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due to...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mahurkar" Elite Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mahurkar Elite Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mahurkar Elite Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ExacTrac 6.0.x Patient Positioning System Recalled by Brainlab AG Due to...
The Issue: ExacTrac 6.0 Patient Positioning System: Display of potentially incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Parsippany Recalled by Biomet Spine, LLC Due to Mislabeling
The Issue: Some of P/N 14-521614B Lot 375440 was mislabeled as P/N 14-521614 Lot 375440.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTISTE Recalled by Siemens Medical Solutions USA, Inc Due to A software fix...
The Issue: A software fix has been released to prevent automatic movement resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natus neoBLUE 3 Phototherapy system or Neonatal Phototherapy Recalled by...
The Issue: The neoBLUE Instruction For Use (IFU) and Service Manuals for the neoBLUE 3...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROFEMUR PLUS CoCr MODULAR NECK Recalled by MicroPort Orthopedics, Inc. Due...
The Issue: Unexpected rate of postoperative fractures resulting in the need for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NebuTech Nebulizer Recalled by Salter Labs Due to The Inspiratory valve cap...
The Issue: The Inspiratory valve cap on the nebulizer reservoir tower may be loose and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Angiographic Injector. Medrad Mark 7 Arterion Injection System Recalled by...
The Issue: Software Version SW 005.006_SH, resulted in the removal of purge enforcement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ferno iNX Wheeled Stretcher Recalled by Ferno-Washington Inc Due to Hole...
The Issue: Hole elongation in the telescoping load frame channel. A hole elongation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Intevo Series system Recalled by Siemens Medical Solutions USA, Inc....
The Issue: Fuses with the improper amperage rating were installed in the Symbia S,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Argyle Infant Heel Warmers (with tab) Item Code: MH00002T Recalled...
The Issue: Infant Heel warmers may break during activation resulting in spillage of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Argyle Infant Heel Warmers (no tab) Item Code: MH00002N Recalled by...
The Issue: Infant Heel warmers may break during activation resulting in spillage of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Symbia S Series system Recalled by Siemens Medical Solutions USA,...
The Issue: Fuses with the improper amperage rating were installed in the Symbia S,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Symbia T Series Recalled by Siemens Medical Solutions USA, Inc. Due...
The Issue: Fuses with the improper amperage rating were installed in the Symbia S,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4 Recalled by Trilliant Surgical Ltd. Due to Gridlock screw driver bits...
The Issue: Gridlock screw driver bits for the Gridlock Plating System were identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.