Resect — Class II medical device recall Z-0779-2021
Terminated recall by Medline Industries Inc, reported 2021-01-13. The cylindrical sponge component is not x-ray detectable.
| Recall number | Z-0779-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medline Industries Inc, Northfield, IL, United States |
| Recall initiated | 2020-11-13 |
| Classified | 2021-01-07 |
| Reported by FDA | 2021-01-13 |
| Terminated | 2021-10-26 |
| Countries outside the US | CA |
| Quantity | 88 |
| Lot numbers | 20GBA365 |
| Model numbers | DYNJ42667A |
| Expiration dates | 2024-11-30 |
Product
Resect. Intest. Laparo-LF, Model DYNJ42667A - Product Usage: This is a type of convenience kit used in various surgeries including cardiac, abdominal, and neck surgeries.
Reason for recall
The cylindrical sponge component is not x-ray detectable.
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-0779-2021. 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.