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. 2,003 recalls have been distributed to Oklahoma in the last 12 months.
Showing 8361–8380 of 28,654 recalls
Recalled Item: Artis icono floor in combination with a Siemens Healthineers table Recalled...
The Issue: Five potential software issues affecting Artis pheno and Artis icono systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniCap Extended Life PD Transfer Set Product Codes: 5C4482S Recalled by...
The Issue: Devices distributed lacked regulatory clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ExacTrac Dynamic software model numbers: 20910-01 Recalled by Brainlab AG...
The Issue: The yaw angle may be incorrect for CBCT positioning workflows using setup...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis pheno- in combination with a Siemens Healthineers table or Recalled by...
The Issue: Five potential software issues affecting Artis pheno and Artis icono systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost C50 1.1 Recalled by Philips North America Llc Due to...
The Issue: Following a system restart where the Table Height 2 (TH2) is the default...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: Product is mislabeled as self-righting Luer slip tip caps, yellow.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpaceOAR Vue System Recalled by Boston Scientific Corporation Due to Users...
The Issue: Users need to be aware that embolism is a possible adverse event associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Regard Custom Procedure Kits containing BD Luer Lok Access Devices Recalled...
The Issue: Recalled devices were packaged in convenience kits.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Outer Packaging Label: Protekt Sharps Safety Knives - 44620MU Recalled by...
The Issue: Surgical knives may contain incorrect description printed on handles....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpaceOAR System Recalled by Boston Scientific Corporation Due to Users need...
The Issue: Users need to be aware that embolism is a possible adverse event associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q ceiling Recalled by Siemens Medical Solutions USA, Inc Due to If the...
The Issue: If the coolant level in the cooling circuit drops below a certain level,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee floor MN Recalled by Siemens Medical Solutions USA, Inc Due to If...
The Issue: If the coolant level in the cooling circuit drops below a certain level,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee multi-purpose Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: If the coolant level in the cooling circuit drops below a certain level,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee biplane MN Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: If the coolant level in the cooling circuit drops below a certain level,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee ceiling Recalled by Siemens Medical Solutions USA, Inc Due to If...
The Issue: If the coolant level in the cooling circuit drops below a certain level,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (a) CareFusion Snowden-Pencer Plastics Recalled by Carefusion 2200 Inc Due...
The Issue: The finished device package did not contain the IFU.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q.zen floor Recalled by Siemens Medical Solutions USA, Inc Due to If...
The Issue: If the coolant level in the cooling circuit drops below a certain level,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee floor Recalled by Siemens Medical Solutions USA, Inc Due to If the...
The Issue: If the coolant level in the cooling circuit drops below a certain level,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q floor Recalled by Siemens Medical Solutions USA, Inc Due to If the...
The Issue: If the coolant level in the cooling circuit drops below a certain level,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q biplane Recalled by Siemens Medical Solutions USA, Inc Due to If the...
The Issue: If the coolant level in the cooling circuit drops below a certain level,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.