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. 2,448 recalls have been distributed to District of Columbia in the last 12 months.
Showing 30001–30020 of 47,654 recalls
Recalled Item: Vertebral Motion Analyzer (VMA) Version 2.3.252. VMA software is a Recalled...
The Issue: Ortho Kinematics Inc. sent a Notice of Correction to Released Testing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L-Varlock Cage/Trial Implant Holder Recalled by Kiscomedica S.A. Due to Firm...
The Issue: Firm received a complaint of the tip holder breaking during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vascular catheter introduction kit The PICC is indicated for short Recalled...
The Issue: There have been complaints for peel away sheaths flaring
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: N Latex HCY REAGENT Recalled by Siemens Healthcare Diagnostics, Inc. Due to...
The Issue: The firm confirmed a reduced once-opened and on-board stability for N Latex...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mammomat Inspiration full Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Software error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Systems Calibrator A Kits Recalled by Siemens...
The Issue: Siemens Healthcare Diagnostics has confirmed a negative bias for ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Systems Calibrator A Kits Recalled by Siemens...
The Issue: Siemens Healthcare Diagnostics has confirmed a negative bias for ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Systems Calibrator A Kits Recalled by Siemens...
The Issue: Siemens Healthcare Diagnostics has confirmed a negative bias for ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIMA Modular Revision Hip Stem Model 428-01-050_110 Product Usage: The...
The Issue: Lima Proximal Bodies were inadvertently re-sterilized. The safety screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Empowr PS Knee Tibial Insert Recalled by Encore Medical, Lp Due to The...
The Issue: The Empowr PS Insert was reported as missing the impaction slot feature.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Docetaxel Injection USP Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Defective Container: Product complaints received of defect in the seal of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Holiday White Peppermint Hostess Twinkies Recalled by Hostess Brands, LLC...
The Issue: Product contains an ingredient that was recalled by a supplier because it...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GN200 Caiman HF generators Recalled by Aesculap Implant Systems LLC Due to...
The Issue: Generators may have a faulty component which could impact the proper...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD NX Sterilization System Recalled by Advanced Sterilization Products...
The Issue: Advanced Sterilization Products (ASP) has identified that in a rare sequence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laerdal Compact Suction Unit ¿ 4 under the following labels: Recalled by...
The Issue: The On/Off functionality in the LCSU 4 is controlled by electronic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Montelukast sodium tablets Recalled by Hetero USA Inc Due to Discoloration:...
The Issue: Discoloration: the firm received a complaint of a sealed bottle in which...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Everroast Chicken Caesar Wrap Recalled by Harris Teeter Due to Undeclared...
The Issue: Undeclared allergen (fish)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DePuy Synthes various orthopedic instruments modified by U.S. Distributors...
The Issue: Products were made outside of Quality System Regulation, and potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C2 CryoBalloon Ablation System - Controller Cap. C2 CryoBalloon Controller...
The Issue: The Controller Cap of the C2 CyroBalloon Ablation System may crack as it is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Color contact lenses labeled under the following brands: Diamond Recalled by...
The Issue: Sterility and Misbranding: Lenses may not be sterile and may be labeled with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.