FDA recall Z-0077-2022

Product

Heparin, GORE VIABAHN VBX, BALLOON EXPANDABLE ENDOPROTHESIS, REF BXAL085902E, 8 MM X 59 MM 8 Fr, LARGE BALLOON EXPANDLBE, Nominal Stent Diameter 8 mm, Max Post-Dilated Stent Diameter 16 mm, UDI:

Reason for recall

Incorrect labeling, specifically, expandable endoprosthesis labeled as 8 mm x 59mm x 135 cm, however may contain a 9mm x 29 mm x 135 cm device.

Distribution

International distribution to the countries of Italy & Lebanon.

Key facts

Status

Ongoing

Initiation date

2021-09-07

Report date

2021-10-20

Voluntary/Mandated

Voluntary: Firm initiated

Location

Flagstaff, AZ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0077-2022