Medline medical procedure kits labeled as follows: a) ARTHROSCOPY — Class II medical device recall Z-2714-2024
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-2714-2024 |
|---|---|
| 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 | 14,977 units |
| UPC / GTIN / UDI-DI | 10193489214413, 10193489967395, 10193489967548, 10193489968026, 10193489968033, 10193489970357, 10193489970418, 10195327040406, 10195327137038, 10195327137199, 10195327214203, 10195327214487, 10195327225377, 10195327360313, 10195327446758, 10195327446918, 10195327468200, 10195327468224, 10195327484262, 10195327493240, 10195327505837, 10195327505899, 10195327507008, 10195327510985, 10195327511012 and 43 more |
| Lot numbers | 22EMA529, 22EMB001, 22EME052, 22EME489, 22EMH888, 22EMI503, 22FBB136, 22FBG650, 22FBK152, 22FBL426, 22FBU282, 22FBW287, 22FMB469, 22FMB880, 22FMD804, 22FMG234, 22FMG260, 22FMH850, 22FMI412, 22GBL020, 22GBN805, 22GBT604, 22GBU282, 22GME946, 22GMG221, 22GMH574, 22GMI092, 22HBA416, 22HBG300, 22HBG372, 22HBS529, 22HBS717, 22HMB217, 22HMD694, 22HMH887, 22IBI040, 22IBI043, 22IBK464, 22IBM480, 22IDA884 and 175 more |
| Model numbers | CDS983991C, CDS984000C, CDS984008C, CDS984009C, DYNJ900847A, DYNJ902367J, DYNJ902368K, DYNJ902380K, DYNJ902619G, DYNJ904767A, DYNJ904769C, DYNJ904771B, DYNJ905511D, DYNJ905512F, DYNJ905513G, DYNJ905514D, DYNJ905518F, DYNJ905519D, DYNJ905852C, DYNJ906273F, DYNJ906274F, DYNJ906275D, DYNJ907157A, DYNJ907158A, DYNJ907159A and 10 more |
Product
Medline medical procedure kits labeled as follows: a) ARTHROSCOPY, REF DYNJ909699; b) BACK CDS, REF CDS984000C; c) EXTREMITY, REF DYNJ900847A; d) HAND-LF, REF DYNJ902619G; e) HIP PINNING CDS, REF CDS984009C; f) HIP PINNING/TFN/ANTERIOR HIP, REF DYNJ902380K; g) KNEE, REF DYNJ904771B; h) KNEE ARTHROSCOPY, REF DYNJ905519D; i) KNEE ARTHROSCOPY, REF DYNJ906273F; j) KNEE ARTHROSCOPY, REF DYNJ909747; k) KNEE ARTHROSCOPY V, REF DYNJS2029D; l) LAMINECTOMY, REF DYNJ907159A; m) LOWER EXTREMITY, REF DYNJ904767A; n) LOWER EXTREMITY, REF DYNJ905518F; o) LOWER EXTREMITY, REF DYNJ909938; p) MINOR EXTREMITY, REF DYNJ909939; q) PODIATRY, REF DYNJ906275D; r) SHOULDER, REF DYNJ904769C; s) SHOULDER, REF DYNJ905511D; t) SHOULDER, REF DYNJ909749; u) SHOULDER ARTHROSCOPY, REF DYNJ906274F; v) SHOULDER ARTHROSCOPY CDS, REF CDS984008C; w) SOUTH EXTREMITY, REF DYNJ909212A; x) SPINE, REF DYNJ905512F; y) TOTAL, REF DYNJ909704; z) TOTAL HIP, REF DYNJ907157A; aa) TOTAL HIP BASIC, REF DYNJ902368K; bb) TOTAL JOINT, REF DYNJ905513G; cc) TOTAL JOINT, REF DYNJ908375C; dd) TOTAL JOINT II, REF DYNJS2027F; ee) TOTAL KNEE, REF DYNJ907158A; ff) TOTAL KNEE CDS, REF CDS983991C; gg) TOTAL SHOULDER, REF DYNJ902367J; hh) TURK-HAND, REF DYNJ905852C; ii) UPPER EXTREMITY, REF DYNJ905514D
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-2714-2024. 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.