FDA recall Z-1798-2024

Product

Medtronic Tourniquet Sets: a) DLP¿ 5.5 in (14.0 cm) Tourniquet Kit, Model Number 79004, b) DLP¿ 7 in (17.8 cm) Tourniquet Kit, Model Number 79009

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-1798-2024