See DocMan — Class II medical device recall Z-0788-2025
Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2025-01-08, distributed nationwide. Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical St
| Recall number | Z-0788-2025 |
|---|---|
| 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 | 2024-11-21 |
| Classified | 2024-12-30 |
| Reported by FDA | 2025-01-08 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, CA |
| Quantity | 65,310 units |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 10193489217155, 10193489263091, 10193489292145, 10193489297706, 10193489320114, 10193489330281, 10193489338386, 10193489345230, 10193489345377, 10193489356809, 10193489390162, 10193489394603, 10193489421491, 10193489446401, 10193489523492, 10193489532227, 10193489547344, 10193489552799, 10193489565942, 10193489568998, 10193489579697, 10193489592030, 10193489596335, 10193489601114, 10193489601930 and 361 more |
| Lot numbers | 100, 101, 102, 103, 104, 105, 106, 107, 108, 109, 110, 111, 112, 113, 114, 115, 116, 117, 118, 119, 120, 121, 122, 123, 124, 125, 126, 127, 128, 129, 130, 131, 132, 133, 134, 135, 136, 137, 138, 139 and 460 more |
| Model numbers | CDS930177C, CDS982054V, CDS982683X, CDS982719X, CDS983467J, CDS983470C, CDS983470I, CDS983799D, CDS985212A, CDS985212B, DYNDA2792, DYNJ0140935G, DYNJ0281906P, DYNJ0545720F, DYNJ0622014R, DYNJ0622359T, DYNJ0622386Q, DYNJ0717887AJ, DYNJ0785885J, DYNJ0842793F, DYNJ0843063I, DYNJ0843063J, DYNJ0843339K, DYNJ0843898D, DYNJ0867427C and 168 more |
Product
See DocMan
Reason for recall
Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
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-0788-2025. 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.