Medline medical procedure kits labeled as follows: a) TURNOVER KIT — Class II medical device recall Z-2710-2024
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-2710-2024 |
|---|---|
| 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 | 160 units |
| UPC / GTIN / UDI-DI | 10195327510916, 40195327510917 |
| Lot numbers | 23LBF766 |
| Model numbers | DYKC1289F |
Product
Medline medical procedure kits labeled as follows: a) TURNOVER KIT, REF DYKC1289F
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-2710-2024. 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.