Medtronic Arterial Cannulae packaged as: a) DLP¿ Curved Metal Tip… — Class II medical device recall Z-1793-2024
Ongoing recall by Medtronic Perfusion Systems, reported 2024-05-22. Potential for unsealed sterile packing.
| Recall number | Z-1793-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic Perfusion Systems, Brooklyn Park, MN, United States |
| Recall initiated | 2024-03-19 |
| Classified | 2024-05-10 |
| Reported by FDA | 2024-05-22 |
| Quantity | 13,033 units |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 00613994879103, 00643169485563, 00643169485570, 00643169485938, 00673978185989, 00673978186009, 00673978187105, 00763000135676, 20613994879107, 20613994879114, 20613994879701, 20643169485468, 20643169485536, 20643169485567, 20643169485574, 20643169485703, 20643169485734, 20643169485741, 20643169485932, 20763000091013, 20763000091020, 20763000091105, 20763000091112, 20763000091174, 20763000091181 and 5 more |
| Lot numbers | 02306C020, 2023031282, 2023031283, 2023031390, 2023031391, 2023040098, 2023040597, 2023040600, 2023040601, 2023040602, 2023040668, 2023040671, 2023040940, 2023040943, 2023040944, 2023040946, 2023040966, 2023040971, 2023040974, 2023040978, 2023040980, 2023041061, 2023041062, 2023041063, 2023041066, 2023041067, 2023041068, 2023041069, 2023041326, 2023041332, 2023041337, 2023041342, 2023041343, 2023041347, 2023041355, 2023041361, 2023041364, 2023041365, 2023041396, 2023041408 and 26 more |
| Model numbers | 72120, 72224, 72424, 77006, 77008, 77010, 77110, 77112, 77206, 77420, 77422, 77522, 77524, 77622, 80020, 80220, 80222, 82020, 87120, 87122, 87220, 87222 |
Product
Medtronic Arterial Cannulae packaged as: a) DLP¿ Curved Metal Tip Arterial Cannula 20 Fr., Model Number 80020; b) DLP¿ Curved Metal Tip Arterial Cannula 20 Fr., Model Number 80220; c) DLP¿ Curved Metal Tip Arterial Cannula 20 Fr., Model Number 82020; d) DLP¿ Curved Metal Tip Arterial Cannula 20 Fr., Model Number 87120; e) DLP¿ Curved Metal Tip Arterial Cannula 22 Fr. , Model Number 80222; f) DLP¿ Curved Metal Tip Arterial Cannula 22 Fr. , Model Number 87122; g) DLP¿ Curved Tip Arterial Cannula 20 Fr., Model Number 87220; h) DLP¿ Curved Tip Arterial Cannula 22 Fr., Model Number 87222; i) DLP" One-Piece Arterial Cannulae, Pediatric 6 Fr, Model Number 77006; j) DLP" One-Piece Pediatric Arterial Cannula 6 Fr, Model Number 77206; k) DLP" One-Piece Pediatric Arterial Cannula 8 Fr, Model Number 77008; l) DLP" One-Piece Pediatric Arterial Cannula 10 Fr, Model Number 77010; m) DLP" One-Piece Pediatric Arterial Cannula 10 Fr, Model Number 77110; n) DLP" One-Piece Pediatric Arterial Cannula 12 Fr, Model Number 77112; o) EOPA" Elongated One Piece Arterial Cannula 20 Fr., Model Number 77420; p) EOPA" Elongated One Piece Arterial Cannula 22 Fr., Model Number 77422; q) EOPA" Elongated One Piece Arterial Cannula 22 Fr., Model Number 77522; r) EOPA" Elongated One Piece Arterial Cannula 22 Fr., Model Number 77622; s) EOPA" Elongated One Piece Arterial Cannula 24 Fr., Model Number 77524; t) Select Series" Angled Tip Arterial Cannula 24Fr., Model Number 72424; u) Select Series" Straight Tip Arterial Cannula 20 Fr., Model Number 72120; v) Select Series" Straight Tip Arterial Cannula 24 Fr., Model Number 72224
Reason for recall
Potential for unsealed sterile packing.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1793-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.