Data Foundry

Medical device recalls 2024

Medtronic Suction Tubes: a) DLP¿ Suction Tube 6-Fr — Class II medical device recall Z-1804-2024

Ongoing recall by Medtronic Perfusion Systems, reported 2024-05-22. Potential for unsealed sterile packing.

Recall numberZ-1804-2024
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMedtronic Perfusion Systems, Brooklyn Park, MN, United States
Recall initiated2024-03-19
Classified2024-05-10
Reported by FDA2024-05-22
Quantity13,198 units
Reason classessterility
UPC / GTIN / UDI-DI00613994570468, 00763000860820, 20613994570448, 20613994570462, 20613994698272, 20613994698319, 20613994698333
Lot numbers2023040913, 2023040914, 2023041164, 2023041269, 2023041270, 2023041271, 2023041273, 2023041274, 2023041275, 2023041277, 2023041278, 2023041279, 2023041281, 2023041282, 2023041284, 2023041285, 202305C056, 202305C057, 202305C071, 202305C072
Model numbers10050, 10052, 10053, 10060, 10061

Product

Medtronic Suction Tubes: a) DLP¿ Suction Tube 6-Fr. Shaft with Frazier Tip, Model Number: 10050, b) DLP¿ Suction Tube 6-Fr. Shaft with 10-Fr. Soft Tip, Model Number: 10052, c) DLP¿ Suction Tube 6-Fr. Shaft with 10-Fr. Soft Tip, Model Number: 10053, d) DLP¿ Suction Tube 10 Fr. Shaft with 20 Fr. Pool Tip, Model Number: 10060, e) DLP¿ Suction Tube 16 Fr. Shaft with 20 Fr. Fluted Tip, Model Number: 10061

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-1804-2024. 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.