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
This recall is currently active, issued May 10, 2024. It was issued by Medtronic Perfusion Systems.
- Company
- Medtronic Perfusion Systems
- Recall Initiated
- March 19, 2024
- Posted
- May 10, 2024
- Recall Number
- Z-1798-2024
- Quantity
- 1760 units
- Firm Location
- Brooklyn Park, MN
- Official Source
- View on FDA website ↗
Reason for Recall
Potential for unsealed sterile packing.
Distribution
Worldwide distribution.
Lot / Code Info
a) Model Number 79004, GTIN 20613994576389, Lot Numbers: 2023081324; b) Model Number 79009, GTIN 20613994576457, Lot Numbers: 2023041000, 2023041384, 202305C235
Root Cause
Process control
Action Taken
Medtronic issued an Urgent Medical Device Recall notice to its consignees on 03/19/2024 via letter (UPS). The notice explained the issue, potential risk, and requested the consignee identify and return the product. Consignee was directed to forward the notice to all affected parties. For questions, the consignee was directed to contact their Medtronic field representative.