Product Recalls in District of Columbia
Product recalls affecting District of Columbia — including food, drugs, consumer products, medical devices, and vehicles distributed to District of Columbia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,411 recalls have been distributed to District of Columbia in the last 12 months.
Showing 39741–39760 of 47,654 recalls
Recalled Item: ADVIA Centaur Immunoassay System Recalled by Siemens Healthcare Diagnostics...
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: V5Ms Transesophageal transducers Recalled by Siemens Medical Solutions USA,...
The Issue: Reports of deterioration of material covering the articulating section of...
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: 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: 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: 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: 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: 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: 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: ENVOY 500 AST Reagent Kit Recalled by ELITech Clinical Systems SAS Due to...
The Issue: Some users of ENVOY 500 AST Reagent Kit, 55255, for Envoy 500 systems are...
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.
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: BD Posiflush Saline Flush Syringe 10 ml inlcuded in the Recalled by Bard...
The Issue: Some unit packages of BD PosiFlush SF Saline Flush Syringe 10 mL may exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Posiflush Saline Flush Syringe 10 ml inlcuded in the Recalled by Bard...
The Issue: Some unit packages of BD PosiFlush SF Saline Flush Syringe 10 mL may exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.