PlainRecalls
FDA Devices Moderate Class II Ongoing

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

Reported: May 22, 2024 Initiated: March 19, 2024 #Z-1798-2024

Product Description

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.

Details

Units Affected
1760 units
Distribution
Worldwide distribution.
Location
Brooklyn Park, MN

Frequently Asked Questions

What product was recalled?
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. Recalled by Medtronic Perfusion Systems. Units affected: 1760 units.
Why was this product recalled?
Potential for unsealed sterile packing.
Which agency issued this recall?
This recall was issued by the FDA Devices on May 22, 2024. Severity: Moderate. Recall number: Z-1798-2024.