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 40641–40660 of 47,654 recalls
Recalled Item: Dextroamphetamine Sulfate Tablets Recalled by Teva Pharmaceuticals USA Due...
The Issue: Failed Impurities/Degradation Specifications: this product is being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Stryker Orthopaedics Triathlon Tritanium Patella Inserter Recalled by...
The Issue: Tritanium Patella Inserter Instrument fracture during implantation. .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PATH(R) THREAD CUP ADAPTOR Recalled by Microport Orthopedics INC. Due to...
The Issue: Difficulty removing the cup adaptor from the impaction handle during surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Hemo software. Merge Hemo monitors Recalled by Merge Healthcare, Inc....
The Issue: The application may crash during the cath lab procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Robotic Arm Interactive Orthopedic System (RIO) Recalled by Mako Surgical...
The Issue: Revision of the field manual
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Organic Cocoa Cassava bars Recalled by Mercola Group Due to Undeclared Milk
The Issue: This voluntary recall has been initiated because the Dr. Mercola Organic...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Convatec Flexi Seal Control Fecal Management System Rx Only by Convatec Inc....
The Issue: Convatec Inc. is recalling Flexi-seal FMS Control Kit since it does not have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes ProDisc-C 2.0mm Milling Bit Recalled by Synthes, Inc. Due to Certain...
The Issue: Certain lots of the ProDisc-C 2.0mm Milling Bits have an increased potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tatiomax (reduced glutathione/hydrolyzed collagen) powder for injection...
The Issue: Marketed Without An Approved NDA/ANDA: Product is sold over the counter...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sterile Water for Injection Recalled by Flawless Beauty LLC Due to Marketed...
The Issue: Marketed Without An Approved NDA/ANDA: Product is sold over the counter...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vitamin C (ascorbic acid) Injection Recalled by Flawless Beauty LLC Due to...
The Issue: Marketed Without An Approved NDA/ANDA: Parenteral product is sold over the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Red Yeast Rice High Potency Dietary Supplement Recalled by Independent...
The Issue: Marketed Without An Approved NDA/ANDA: Product is being recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Laroscorbine Platinium (vitamin C/collagen) injectable I.V. solution...
The Issue: Marketed Without An Approved NDA/ANDA: Product is sold over the counter...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Saluta (reduced glutathione) Powder for Injection Recalled by Flawless...
The Issue: Marketed Without An Approved NDA/ANDA: Parenteral product is labeled for use...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Relumins Advanced Glutathione (lyophilized glutathione/vitamin C) injectable...
The Issue: Marketed Without An Approved NDA/ANDA: Product is sold over the counter...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp Recalled by...
The Issue: Connection issues between the PD transfer set catheter connector and an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coaxial Micro-Introducer Kit. Greatbatch Part Number/Bard Access Systems...
The Issue: Greatbatch identified that the documentation does not support the five-year...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 2008T Hemodialysis Machine with Revision K Actuator Test Boards...
The Issue: 2008-Series Hemodialysis Machines with Revision K Actuator Test Boards may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revision K Actuator Test Boards sold as replacement parts for Recalled by...
The Issue: 2008-Series Hemodialysis Machines with Revision K Actuator Test Boards may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation software version 4.0.3.4 RayStation is a software system designed...
The Issue: This notice concerns a problem with the computation of ROI voxel volumes for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.