Medline medical procedure kits labeled as follows: a) AAA CDS — Class II medical device recall Z-2708-2024
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-2708-2024 |
|---|---|
| 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 | 75,098 units |
| UPC / GTIN / UDI-DI | 10193489244731, 10195327044206, 10195327044978, 10195327045012, 10195327045036, 10195327314712, 10195327446901, 10195327505844, 10195327510992, 10195327511210, 10888277745902, 10888277877023, 10889942279371, 10889942325795, 10889942750153, 10889942805747, 10889942925353, 40193489244732, 40195327044207, 40195327044979, 40195327045013, 40195327045037, 40195327314713, 40195327446902, 40195327505845 and 9 more |
| Lot numbers | 22EBC452, 22EBF069, 22EMC363, 22FBC759, 22FBD067, 22FBW468, 22FBX932, 22FLA082, 22FLA559, 22FMA812, 22FMD877, 22FMF770, 22FMF873, 22FMH475, 22GBR344, 22GBW830, 22GLA027, 22GLA591, 22GMD228, 22HBG632, 22HBM538, 22HBU819, 22HMF347, 22HMF787, 22HMH211, 22HMH348, 22HMH967, 22IBT843, 22IBU640, 22ILA148, 22IMH596, 22JBR362, 22JBW467, 22JMD898, 22KBE842, 22KBK453, 22KBS235, 22KMH402, 22LBC023, 22LMC603 and 74 more |
| Model numbers | CDS984010B, CDS984011C, DYK1253578F, DYKC1274A, DYKC1309A, DYKE1516A, DYKE1830, DYKE1898, DYKM1184, DYKM1187A, DYKM2126, DYKM2127, DYKM2128, DYNJ902374K, DYNJ909703, DYNJ909937, DYNJ909940 |
Product
Medline medical procedure kits labeled as follows: a) AAA CDS, REF CDS984011C; b) CAN KIT, REF DYKM1184; c) DENTAL CDS, REF CDS984010B; d) EGD KIT, REF DYK1253578F; e) EGD REG KIT, REF DYKE1830; f) ENDO KIT, REF DYKE1516A; g) ERCP REG KIT, REF DYKM2127; h) GI PACK, REF DYKE1898; i) KIT, PEG, REG, REF DYKM2128; j) KIT,1500CC, 50CS, REF DYKM2126; k) LITHOTOMY, REF DYNJ909937; l) MAJOR BASIC, REF DYNJ909703; m) MINOR GENERAL SURGERY, REF DYNJ909940; n) SUCTION SET UP KIT, REF DYKM1187A; o) TURNOVER KIT, REF DYKC1274A; p) TURNOVER KIT MKT STRAPS, REF DYKC1309A; q) U BAR, REF DYNJ902374K
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-2708-2024. 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.