Reported May 22, 2024 · Ongoing
Medtronic Tourniquet Sets: a) DLP¿ 5.5 in (14.0 cm) Tourniquet Kit, Model Number 79004, b) DLP¿ 7 in (17.8 cm)…
Medtronic Perfusion Systems
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Medtronic Perfusion Systems · 7611 Northland Dr N · Brooklyn Park, MN · 55428-1088
Is this the product you have?
- Medtronic Tourniquet Sets
a) DLP¿ 5.5 in (14.0 cm) Tourniquet KitModel Number 79004b) DLP¿ 7 in (17.8 cm) Tourniquet KitModel Number 79009
- Lot codes and dates
a) Model Number 79004GTIN 20613994576389
- Lot Numbers
2023081324b) Model Number 79009GTIN 20613994576457
- Lot Numbers
20230410002023041384202305C235
- Amount recalled
- 1760 units
This recall covers 13 products
The agency filed one notice per product. You are reading one of them; the other 12 are below.
Why it was recalled
Potential for unsealed sterile packing.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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