MEDLINE STERILE BASIC EYE PACK 16: 1) REF: DYNJ37743D — Class II medical device recall Z-0510-2026
Ongoing recall by Medline Industries, LP, reported 2025-11-26. Medline has identified specific sterile eye procedure kits with pouch packaging that may exhibit open seals.
| Recall number | Z-0510-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medline Industries, LP, Northfield, IL, United States |
| Recall initiated | 2025-10-03 |
| Classified | 2025-11-14 |
| Reported by FDA | 2025-11-26 |
| Quantity | 1,024 units |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 10193489600124, 10198459390685, 40193489600125, 40198459390686 |
| Lot numbers | 25EMI333, 25GMD927 |
| Model numbers | DYNJ37743D, DYNJ37743F |
Product
MEDLINE STERILE BASIC EYE PACK 16: 1) REF: DYNJ37743D; 2) REF: DYNJ37743F.
Reason for recall
Medline has identified specific sterile eye procedure kits with pouch packaging that may exhibit open seals.
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-0510-2026. 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.