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. 2,429 recalls have been distributed to District of Columbia in the last 12 months.
Showing 35401–35420 of 47,654 recalls
Recalled Item: Morphine Sulfate (PF) 0.1 mg/mL in 0.9% Sodium Chloride Recalled by...
The Issue: Stability data does not support expiry.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Provocholine Pre-diluted Set II in 0.9% Sodium Chloride Recalled by...
The Issue: Stability data does not support expiry.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ACUSON SC2000 Ultrasound System with software versions VB10B and lower...
The Issue: The ACUSON SC2000 ultrasound system considers uppercase/lowercase...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediTrace Cadence Adult Zoll Recalled by Covidien LLC Due to Multi-Function...
The Issue: Multi-Function Defibrillation Electrodes, Pre connect- potential for damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Physio-Control QuikCombo Pacing/Defibrillation/ECG Electrodes RediPak¿...
The Issue: Multi-Function Defibrillation Electrodes, Pre connect- potential for damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediTrace Cadence Adult Multi-Function Defibrillation Electrodes Item...
The Issue: Multi-Function Defibrillation Electrodes, Pre connect- potential for damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Actifuse ABX/Actifuse MIS System A bone void filler intended only Recalled...
The Issue: Baxter Healthcare is issuing a voluntary recall for all lots of Actifuse ABX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Force Recalled by Siemens Medical Solutions USA, Inc Due to Software...
The Issue: Software and firmware bugs
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Marker Spheres The Disposable Marker Spheres used Recalled by...
The Issue: Disposable Marker Spheres (DRMS) for Brainlab Image Guided Surgery (IGS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microtek Medical Recalled by Ecolab Inc Due to The sterile packaging may...
The Issue: The sterile packaging may contain small (less than 250 microns wide)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PenBlade Safety Scalpel Recalled by Zien Medical Technologies, Inc Due to...
The Issue: Cracks were discovered in the PET tray of a small population of sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin@home RF Remote Monitoring Transmitter Model EX1150. Intended to aid...
The Issue: Some devices exhibit backup VVI operation due to a backup reset.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDTRONIC PERFUSION TUBING PACKS (with potentially affected...
The Issue: Hemocor High Performance Hemoconcentrators demonstrate low ultrafiltration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDIVATORS HEMOCOR HPH700 Recalled by Medtronic Perfusion Systems Due to...
The Issue: Hemocor High Performance Hemoconcentrators demonstrate low ultrafiltration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cevimeline Hydrochloride Capsules Recalled by Apotex Inc. Due to Failed...
The Issue: Failed Stability Specifications: product may not meet specification limit...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bromfenac Ophthalmic Solution Recalled by Bausch & Lomb, Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Failed preservative effectiveness testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CIOS ALPHA Recalled by Siemens Medical Solutions USA, Inc Due to patient...
The Issue: patient procedure interruption due to a potential system failure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Xi Surgical System P4 software Recalled by Intuitive Surgical, Inc....
The Issue: Complaints regarding the Exposed Knife Blade recoverable fault for the Xi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFX-8000V Bi-Plane X-Ray Interventional System X-ray systems Recalled by...
The Issue: When a fontal DA (Digital Angiography) acquisition was done, scattered x-ray...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: software bug issues for SW-Version VA48A_SP0. The following safety issues...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.