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. 2,464 recalls have been distributed to District of Columbia in the last 12 months.
Showing 22961–22980 of 27,451 recalls
Recalled Item: ST¿CKERT HeaterCooler System 3T Recalled by Sorin Group USA, Inc. Due to On...
The Issue: On August 1, 2014 Sorin Group USA, Inc. informed consignees via letter to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pinnacle3 Software Version 9.0 Recalled by Philips Electronics North America...
The Issue: Philips, Pinnacle Radiation Treatment Planning System version 8.0h, 8.0k,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mindray V21 Recalled by Mindray DS USA, Inc. dba Mindray North America Due...
The Issue: Mindray DS USA Inc. initiated a voluntary field corrective action for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roche cobas IT 1000 Product Usage: Intended Use: An electronic Recalled by...
The Issue: Potential that test results would be assigned to the wrong Patient ID if...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion AirLife Heated Infant Breathing Circuit Product Usage:...
The Issue: The CareFusion AirLife Heated Infant Breathing Circuit is being recalled due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW II 2 HOLE PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Gender Solution Patello-Femoral Joint (PFJ) System Patello-Femoral...
The Issue: Internal review found that five (5) PFJ implant forgings were identified as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW II 2 HOLE PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW II STRAIGHT PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW II STRAIGHT PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW 3.5mm PLATE CHARLOTTE F&A SYSTEM Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW II 2 HOLE PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW II STRAIGHT PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW PLATE 20mm INTERAXIS CHARLOTTE F&A SYSTEM Recalled by Wright Medical...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAW II 2 HOLE PLATE ORTHOLOC 3DSi Recalled by Wright Medical Technology,...
The Issue: Plates manufactured from an incorrect raw material.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Illumina Worklist Manager (IWM) (software v1.0.15) Recalled by Illumina Inc...
The Issue: A software component of the MiSeqDx instrument, called the Illumina Worklist...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minstrel (with scale) Product Usage: is a mobile passive hoist. Recalled by...
The Issue: ArjoHuntleigh received three reports where the bolt under the scale...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL Vancomycin Screen Agar Catalog number 222204 Vancomycin Screen...
The Issue: These lots of Agar may have exhibited breakthrough growth of vancomycin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RADIANCE v. 2.4X Recalled by Radiometer America Inc Due to
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GALT VALVED TEARAWAY INTRODUCER SET GALT VTI RX ONLY UNITS Recalled by Galt...
The Issue: The adhesive used in the product could dislodge when objects are inserted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.