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 39801–39820 of 47,654 recalls
Recalled Item: Ortho Molecular Products LifeCORE Complete Recalled by Ortho Molecular...
The Issue: Ortho Molecular Products is recalling all lots of LifeCore Chocolate and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ortho Molecular Products LifeCORE Recalled by Ortho Molecular Products Inc...
The Issue: Ortho Molecular Products is recalling all lots of LifeCore Chocolate and...
Recommended Action: Do not consume. Return to store for a refund or discard.
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: CYTARAbine for Injection USP Recalled by Ben Venue Laboratories Inc Due to...
The Issue: Lack of Assurance of Sterility: Crimp defects during visual inspection could...
Recommended Action: Stop taking this medication. Contact your pharmacy or 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: 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: 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: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...
The Issue: Lack of Assurance of Sterility; complaints of mold in the overpouch
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Depo-Medrol (methylprednisolone acetate injectable suspension USP) Recalled...
The Issue: Failed pH Specification: A pH result of 2.9 was obtained at the 9 month...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cataflam (diclofenac potassium) tablets Recalled by Novartis Pharmaceuticals...
The Issue: Failed Tablet/Capsule Specifications: Ink identification had rubbed off...
Recommended Action: Stop taking this medication. Contact your pharmacy or 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 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: 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 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 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 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.