Medline convenience kits labeled as: 1) LAMI FUSION — Class II medical device recall Z-3029-2026
Ongoing recall by Medline Industries, LP, reported 2026-09-02, distributed nationwide. Kits contain a potentially contaminated component which were recalled by the manufacturer
| Recall number | Z-3029-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medline Industries, LP, Northfield, IL, United States |
| Recall initiated | 2026-07-10 |
| Classified | 2026-08-26 |
| Reported by FDA | 2026-09-02 |
| Distributed | Nationwide (US) |
| Quantity | 241 kits |
| UPC / GTIN / UDI-DI | 10198459255069, 10198459385636, 10198459419614, 10198459539374, 40198459255060, 40198459385637, 40198459419615, 40198459539375 |
| Lot numbers | 25JBM473, 25JML577, 25KLA074, 25LMF531, 26CDA102, 26DDA481, 26DDB085 |
Product
Medline convenience kits labeled as: 1) LAMI FUSION, Medline Kit SKU CDS982035Y; 2) NON MB MJR NEURO CRANI SM PK, Medline Kit SKU DYNJT6104; 3) CRANIOTOMY, Medline Kit SKU DYNJ903471I; 4) KIT CRANIOTOMY RFD, Medline Kit SKU DYNJ906496K.
Reason for recall
Kits contain a potentially contaminated component which were recalled by the manufacturer
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-3029-2026. 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.