SCISSORS — Class II medical device recall Z-0921-2026
Ongoing recall by Medline Industries, LP, reported 2025-12-24, distributed nationwide. The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lea
| Recall number | Z-0921-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medline Industries, LP, Northfield, IL, United States |
| Recall initiated | 2025-11-13 |
| Classified | 2025-12-12 |
| Reported by FDA | 2025-12-24 |
| Distributed | Nationwide (US) |
| Quantity | 56 units |
| Reason classes | sterility, packaging |
| UPC / GTIN / UDI-DI | 10193489191349, 20193489191346 |
| Lot numbers | 2023102590 |
| Model numbers | DYND04000 |
Product
SCISSORS, OR, SHARP/BLUNT, 5.5", STERILE, Item Number DYND04000
Reason for recall
The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if product is utilized.
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-0921-2026. 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.