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. 2,459 recalls have been distributed to District of Columbia in the last 12 months.
Showing 23601–23620 of 27,451 recalls
Recalled Item: Anspach Pneumatic and Electric Motor Systems. Intended for cutting and...
The Issue: Several attachments and handpieces failed to meet the expected sterility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Devon Supine Recalled by Covidien LLC Due to Straps may separate from the...
The Issue: Straps may separate from the foam pad.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G7 Acetabular System Positioning Guide Post Recalled by Biomet, Inc. Due to...
The Issue: Guide rod may fracture during impaction of the acetabular shell and be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G7 Acetabular System Positioning Guide Rod Recalled by Biomet, Inc. Due to...
The Issue: Guide rod may fracture during impaction of the acetabular shell and be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Visitec Anterior Chamber Cannula Recalled by Beaver-Visitec International...
The Issue: Contains a sharp tip needle when the product should contain a blunt tip cannula
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens LANTIS System Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: There is a potential risk when using LANTIS OIS System client software with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVOCATE Redi-Code+ BMB-BA006A Blood Glucose test strips Product Usage: The...
The Issue: "Advocate Redi-Code + BMB-BA006A Blood Glucose test strips" are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kenex Radiation Shield and surgical lamps installed with GE Healthcare...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Triage¿ D-Dimer Test PN 98100 Recalled by Alere San Diego, Inc. Due to...
The Issue: Alere initiated this recall because a limited number of Alere Triage¿...
Recommended Action: Stop using. Contact the manufacturer or your 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: 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: 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: 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: 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: 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: 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.
Recalled Item: BG3515-5 US 5mL BioGlue Surgical Adhesive. BioGlue Surgical Adhesive...
The Issue: Serum albumin component monomer failed to meet internally established end of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.