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. 2,468 recalls have been distributed to Oklahoma in the last 12 months.
Showing 25701–25720 of 28,654 recalls
Recalled Item: chromID Salmonella Agar Recalled by bioMerieux, Inc. Due to Potential...
The Issue: Complaints for Salmonella strains growing on this medium producing an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PREMIER CARE RECLINER 5570 with Urethane armrests Recalled by Winco Mfg.,...
The Issue: A supplier manufacturing assembly defect with the right hand recline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XL CONVALESCENT RECLINER 5291/529S with Padded armrests with guard Recalled...
The Issue: A supplier manufacturing assembly defect with the right hand recline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: AVEA¿ Ventilator. All Models. The affected devices are...
The Issue: CareFusion has identified a potential risk associated with AVEA¿ ventilators...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cranial Access (CRAK) Kits Recalled by Integra LifeSciences Corp. d.b.a....
The Issue: Integra is recalling certain lots of Cranial Access Kit due to a possibility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter CLEARLINK System Non-DEHP Three Lead Extension Set. 6.0" (15 cm)...
The Issue: The firm is issuing a voluntary recall due to the potential for pinholes in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 1800 System Software V2.01. Performs assays for general and Recalled...
The Issue: Siemens Healthcare Diagnostics issued a Urgent Medical Device Correction due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 1650 System Software: 1) V4.01 Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics issued a Urgent Medical Device Correction due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blanketrol III Recalled by Cincinnati Sub-Zero Products Inc Due to During a...
The Issue: During a label review it was discovered that both the Blanketrol III...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT is a gamma camera for Single Photon Emission Recalled by...
The Issue: Philips received reports from the field that the Flat Panel Detector (FPD)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 1200 System Software: 1) V2.00 Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics issued a Urgent Medical Device Correction due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAD Fluoro Uro system (Luminos dRF and Uroskop Omnia Recalled by...
The Issue: When using systems operating with software versions VD10A/G during a RAD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (Siemens Rad Fluoro Uro Systems) Ysio Recalled by Siemens Medical Solutions...
The Issue: A potential malfunction and hazard to patients exists when using the Ysio,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2400 System Software V4.01. Performs assays for general and Recalled...
The Issue: Siemens Healthcare Diagnostics issued a Urgent Medical Device Correction due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoCr Head (Not distributed in the United States) Used in Recalled by Zimmer,...
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen CR-Flex Mobile Bearing Tibial Component 9 (Not distributed in...
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Emit 2000 Phenobarbital Assay and Syva Emit 2000 Phenobarbital Assay...
The Issue: Imprecision with certain lots
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen¿ Femoral Component (CR-FLEX GSF POR FEM Recalled by Zimmer, Inc. Due...
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen¿ Femoral Component (CR-FLEX GSF PRECOAT SZ C-L Recalled by Zimmer,...
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a potential safety issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.