Medline medical procedure kits labeled as follows: a) CYSTO — Class II medical device recall Z-2704-2024
Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2024-08-28, distributed nationwide. A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
| Recall number | Z-2704-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | MEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States |
| Recall initiated | 2024-03-22 |
| Classified | 2024-08-22 |
| Reported by FDA | 2024-08-28 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, CO, MX, OM, PA, QA, SG, SV |
| Quantity | 22,891 units |
| UPC / GTIN / UDI-DI | 10193489214154, 10193489424942, 10193489970272, 10193489970340, 10193489970524, 10193489978278, 10193489978599, 10195327137182, 10195327269074, 10195327316907, 10195327316945, 10195327421366, 10195327442224, 10195327468217, 10195327511036, 10889942620166, 10889942632312, 40193489214155, 40193489424943, 40193489970273, 40193489970341, 40193489970525, 40193489978279, 40195327137183, 40195327269075 and 8 more |
| Lot numbers | 22EBN239, 22EME324, 22EMG657, 22EMH533, 22FBF410, 22FBM118, 22FBQ906, 22FDC042, 22FME336, 22FMG304, 22FMH099, 22FMH851, 22GBV826, 22HMH828, 22IBL707, 22IMA134, 22IMA525, 22IMD626, 22JBS556, 22JDA825, 22JDB988, 22JMC383, 22JMF012, 22KBJ795, 22KME231, 22LBB636, 22LBJ315, 22LDB688, 22LMB229, 22LMC594, 22LME429, 22LME748, 22LMF477, 22LMF668, 22LMI027, 23ABD205, 23ABF810, 23ABL864, 23ABM564, 23ABS802 and 78 more |
| Model numbers | DYKE1431B, DYKE1462A, DYKE1623B, DYNJ902288I, DYNJ902383I, DYNJ902385I, DYNJ904768B, DYNJ905000D, DYNJ905005C, DYNJ905508G, DYNJ905520F, DYNJ9062767D, DYNJ907154A, DYNJ907155A, DYNJ907187A, DYNJ909748, DYNJS2032D |
Product
Medline medical procedure kits labeled as follows: a) CYSTO, REF DYNJ905000D; b) ENDO KIT, REF DYKE1462A; c) ENDOSCOPY KIT, REF DYKE1431B; d) ENDOSCOPY KIT, REF DYKE1623B; e) GENERAL LAPAROSCOPY, REF DYNJ902385I; f) GENERAL LAPAROSCOPY, REF DYNJ905508G; g) GENERAL LAPAROSCOPY V, REF DYNJS2032D; h) LAP APPY, REF DYNJ902383I; i) LAP CHOLE, REF DYNJ9062767D; j) LAP CHOLE, REF DYNJ907187A; k) MAJOR, REF DYNJ904768B; l) MAJOR, REF DYNJ905520F; m) MAJOR, REF DYNJ907154A; n) MAJOR SURGICAL, REF DYNJ905005C; o) MINOR, REF DYNJ907155A; p) MINOR SET UP, REF DYNJ909748; q) RHYZOTOMY, REF DYNJ902288I;
Reason for recall
A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
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-2704-2024. 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.