FDA recall Z-1799-2024

Product

Medtronic Vessel Cannulae: a) DLP¿ 2 mm Vessel Cannula Blunt Tip, Model Number 30004; b) DLP¿ 3 mm Vessel Cannula Blunt Tip, Model Number 30003

Reason for recall

Potential for unsealed sterile packing.

Distribution

Worldwide distribution.

Key facts

Status

Ongoing

Initiation date

2024-03-19

Report date

2024-05-22

Voluntary/Mandated

Voluntary: Firm initiated

Location

Brooklyn Park, MN, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1799-2024