FDA recall Z-0076-2019

Angiodynamics Inc. (Navilyst Medical Inc.) · Class II · device

Product

BioFlo Port with ENDEXO and PASV Technology-AngioDynamics BIOFLO 8F SINGLE PLASTIC NON-FILLED; VALVED PG UPN: H965440210 Catalog Number: 44-021 Box of 1 Port - Product Usage - Long-term access to the central venous system for administration of fluids including but not limited to hydration fluids, chemotherapy, analgesics, nutritional therapy and blood products. The device is also indicated for blood specimen withdrawal.

Reason for recall

BioFlo Ports was partially manufactured with the incorrect sterile port assembly. The actual sterile port assembly used was, 8F SL Xcela Plus Titanium Valved Non-Filled, when it should have been, 8F SL BioFlo Plastic Valved Non-Filled

Distribution

US Nationwide in the state of IN.

Key facts

Status
Terminated
Initiation date
2018-07-24
Report date
2018-10-17
Termination date
2019-05-17
Voluntary/Mandated
Voluntary: Firm initiated
Location
Glens Falls, NY, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0076-2019