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. 2,485 recalls have been distributed to District of Columbia in the last 12 months.
Showing 20901–20920 of 27,451 recalls
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...
The Issue: When performing head or neck scans, the currently displayed SAR values could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConFormis iTotal Posterior Stabilized Knee Replacement System- ITOTAL...
The Issue: May contain small amounts of ethylene glycol residue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to When performing head or neck...
The Issue: When performing head or neck scans, the currently displayed SAR values could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConFormis iTotal CR Knee Replacement System- iTOTAL CR Recalled by...
The Issue: May contain small amounts of ethylene glycol residue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConForMIS iDuo Knee Bicompartmental Knee Replacement System Recalled by...
The Issue: May contain small amounts of ethylene glycol residue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConForMIS iDuo Bicompartmental Knee Replacement System iDUO G2 Recalled by...
The Issue: May contain small amounts of ethylene glycol residue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConForMIS iUni Unicondylar Knee Replacement System- iUNI G2 Recalled by...
The Issue: May contain small amounts of ethylene glycol residue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConForMIS iUNI Unicondylar Knee Replacement System iUNI G2 Recalled by...
The Issue: May contain small amounts of ethylene glycol residue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Cranial Flap Tube Clamp and Crimping Device Product Usage: Recalled...
The Issue: The Synthes Cranial Flap Tube Clamp and Crimping Device for Cranial Tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Guide Wires for orthopedic procedures. Recalled by Zimmer, Inc. Due...
The Issue: Product labeling of these sterile guide wires (external carton label and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Kits with Medtronic Covidien 0.9% Sodium Chloride Flush Syringes...
The Issue: Manufacturer of 0.9% Sodium Chloride Flush Syringes recalled due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CD4 (SK3) Recalled by Becton, Dickinson and Company, BD Biosciences Due to...
The Issue: CD4 FITC label contains an error in the Spanish small text - it states CD8 FITC.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD AffirM VPIII Microbial Identification Test Recalled by Becton Dickinson &...
The Issue: BD has confirmed that a portion of tests associated with the affected lots(...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Cholestech LDX Multianalyte Controls Recalled by Alere San Diego, Inc....
The Issue: Alere San Diego is recalling the Alere Cholestech LDX Multianalyte Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThruPort Knot Pusher. This device is sold individually (Model KP1) Recalled...
The Issue: The configuration of the slot at the tip of the knot pusher may inhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo Lab Data Manager System - Product Usage: syngo Lab Recalled by Siemens...
The Issue: Software Issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to...
The Issue: Cross-threading of the hemostasis valve may occur if it is tightened with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to...
The Issue: Cross-threading of the hemostasis valve may occur if it is tightened with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ambitex NMD400 Nitrile Exam Gloves size medium. General Hospital and...
The Issue: Ambitex Nitrile NMD400 Exam Gloves size medium on exam hold were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAPIDPoint 500 Measurement Cartridge Lactate (750 tests) Part...
The Issue: RAPIDPoint 500 measurement cartridge serial numbers 2517102517 through...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.