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. 959 recalls have been distributed to Oklahoma in the last 12 months.
Showing 41561–41580 of 49,976 recalls
Recalled Item: ADVIA Centaur XP Immunoassay System Recalled by Siemens Healthcare...
The Issue: The firm is conducting a field correction for the ADVIA Centaur and ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...
The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...
The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...
The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acrobat V Vacuum Off-Pump System OM-9100S Acrobat SUV Vacuum Off-Pump...
The Issue: An internal finding identified the presence of pinholes/cuts in some of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENASYS EZ Negative Pressure Wound Therapy (NPWT) System (RENASYS EZ)...
The Issue: Modification were made to the RENASYS EZ NPWT Systems without a 510(k) or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Water may leak...
The Issue: Water may leak into the center gas lumen of the Patient Circuit
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...
The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...
The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...
The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...
The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JBAIDS Instrument System Software version 3.5.0.72. The JBAIDS instrument is...
The Issue: BioFire Defense, LLC is initiating a field action for JBAIDS Software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROPRANOLOL HYDROCHLORIDE INJECTION Recalled by Fresenius Kabi USA, LLC Due...
The Issue: CGMP Deviations: Citations given to API supplier by the Italian Health...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: METOCLOPRAMIDE ORAL SOLUTION Recalled by VistaPharm, Inc. Due to Defective...
The Issue: Defective Container: Product leaks when inverted.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: McCormick Ground Oregano in 0.75 oz plastic bottle. NUMBER: Recalled by...
The Issue: Retail sample of ground oregano tested positive for Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PROXIMATE Skin Stapler. PROXIMATE RH Rotating-Head Skin Stapler (Model...
The Issue: The device may have a non-conforming component that may cause the device to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: eXpertDC intraoral x-ray Recalled by Gendex Corp Due to Two (2) failures of...
The Issue: Two (2) failures of the spring link components within the articulated arm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Luminos dRF system with SW VD10 or on Luminos Recalled by Siemens...
The Issue: It was determined that a potential malfunction may occur on the Luminos dRF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neodent Titamax WS Cortical Implant ¿4.0 x 5 mm (Endosseous Recalled by...
The Issue: Product not approved for use in the US
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABX PENTRA Magnesium RTU Reagent Recalled by Horiba Instruments, Inc dba...
The Issue: Horiba Medical is recalling the ABX PENTRA Magnesium RTU Reagent because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.