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. 2,459 recalls have been distributed to District of Columbia in the last 12 months.
Showing 23721–23740 of 27,451 recalls
Recalled Item: SBi RingFix Olive Wires Product Usage: These are temporary devices Recalled...
The Issue: Small Bone Innovations (SBI) is recalling non-sterile RingFIX Olive Wires...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model RG3000 and RG4000 Series Valve Integrated Pressure Regulator (VIPR)...
The Issue: Separation events have occurred, including the VIPR separating from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit 8551/856X (includes Models 8561 Recalled by Medtronic Neuromodulation...
The Issue: Some kits in the affected lots may contain an extension tubing set that is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lithium Ion Battery M4605A and M4607A for use with IntelliVue Recalled by...
The Issue: The risk of battery failure increases with age, when a battery remains in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iLab Ultrasound Imaging System Recalled by Boston Scientific Corporation Due...
The Issue: Specific iLab Ultrasound Imaging Systems using newest 3.0 (Polaris 1.0)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Centricity PACS Workstation is intended for use as a Recalled by GE...
The Issue: It has been identified that in a reject image workflow where multiple...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo Imaging XS Syngo Imaging XS is a Picture Archiving Recalled by Siemens...
The Issue: A complaint reported that the archiving method at one customer site was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sprotte Spinal Tray / Sprotte Spinal Needle 24 gauge with Recalled by B....
The Issue: B.Braun Medical, Inc. (BBMI) has received reports of 24 gauge Sprotte...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medrad Continuum MR Infusion system- non-wireless system The MEDRAD...
The Issue: There is a potential safety risk associated with potentially damaged locking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shimadzu Digital Radiography X-Ray System Recalled by Shimadzu Medical...
The Issue: Shimadzu Corporation is recalling the Shimadzu Digital X-Ray System because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo Dynamics v9.5 system. A Picture Archiving and Communication System...
The Issue: Systems with the affected serial number are experiencing a software error...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMIA v1.0 APD System. For Automated Peritoneal Dialysis (APD) therapy...
The Issue: Additional warning in the AMIA APD System labeling for patients vulnerable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ACUSON X700 Ultrasound Systems with software version 1.0.00 Recalled...
The Issue: When fourSight 4D ultrasound imaging, 3-Scrape real time 3D imaging, or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Circular Lock Screws Recalled by Genesys Orthopedics Systems, LLC Due to The...
The Issue: The recall is being initiated because MK Precision (the Circular Lock Screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to Potential safety issue...
The Issue: Potential safety issue with gradient coil electromechanical connections...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABACUS TPN Calculation Software Recalled by Baxter Corporation Englewood Due...
The Issue: 1. ABACUS v3.1 may calculate quantities of electrolytes that are double the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart XL+ Defibrillator/Monitor with system software version...
The Issue: Software communication failure may occur on the HeartStart XL+ locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PS-C Femoral Nonporous Rt Sz 6 Recalled by Ortho Development Corporation Due...
The Issue: A femoral component containing pegs was found in a box for the pegless version.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Medical Systems Computed Tomography X-ray systems (Brilliance CT...
The Issue: A customer reported that the table top had become free floating. A Field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 550 TxT Treatment Table of the Digital Linear Accelerator (LINAC) Recalled...
The Issue: Table may lose calibration during patient treatment, which may cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.