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. 2,654 recalls have been distributed to Oklahoma in the last 12 months.
Showing 5341–5360 of 28,654 recalls
Recalled Item: Alinity c Processing Module The Alinity c Processing Recalled by Abbott...
The Issue: The devices contain a dry natural rubber (latex) subcomponent, which are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity i Processing Module The Alinity i Processing Recalled by Abbott...
The Issue: The devices contain a dry natural rubber (latex) subcomponent, which are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Clean Stool Transportation System-For the collection...
The Issue: Due to a manufacturing defect, certain Para-Pak vials may be at risk for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Para-Pak Zn-PVA/10% Formalin-for the routine collection Recalled by Meridian...
The Issue: Plastic vials contain a manufacturing defect may cause an increased risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: epoc NXS Host Blood Analysis System Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics Inc. has confirmed a potential issue that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Para-Pak Clean Vial-For the collection Recalled by Meridian Bioscience Inc...
The Issue: Plastic vials contain a manufacturing defect may cause an increased risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Cranial Access Kit - For access to the subarachnoid Recalled by...
The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Cranial access kit (without Prep solutions) Bit and Guard-For...
The Issue: Defect in the outer packaging of the Cranial Access Kits can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Combo Kit Consists OF 10-110/INS-4500/INS-7040- For access to the...
The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra¿ Cranial Access Kit-For access to the subarachnoid space or Recalled...
The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Cranial Access Kit- For access to the subarachnoid space Recalled by...
The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Cranial Access Kit-For access to the subarachnoid space or Recalled...
The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Cranial Access Kit-For access to the subarachnoid space or Recalled...
The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LYFO-DISK Recalled by Microbiologics Inc Due to A complaint investigation...
The Issue: A complaint investigation showed that the bulk pellets (lot 794-142) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KWIKSTIK Recalled by Microbiologics Inc Due to A complaint investigation...
The Issue: A complaint investigation showed that the bulk pellets (lot 794-142) were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS icono (ceiling configuration) Recalled by Siemens Medical Solutions...
The Issue: Potential hardware issue for ARTIS icono ceiling system: collision sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOFIRE Blood Culture Identification 2 (BCID2) Panel Recalled by BioFire...
The Issue: Routine quality control testing of affected blood culture identification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray TORCH . HTFA-ASY-0104 is the BIOFIRE TORCH Base Recalled by...
The Issue: Due to an increased risk of degradation of the power entry switch resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tracheostomy care kits: (1) Medline Tracheostomy Clean and Care Tray...
The Issue: The component tracheostomy brush has a sharp edge at the tip that can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vitality Polyaxial Screw Recalled by Zimmer Biomet Spine Inc. Due to Spinal...
The Issue: Spinal fixation system 7.5mmx 50mm screws are packaged with the correct...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.