MEDLINE ARTERIAL LINE PACK — Class II medical device recall Z-1049-2025
Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2025-02-05, distributed in FL, IL, KS, ND, PA, WA, WV. Certain lots Sterile Infusion Catheters which were mislabeled as having a heparin coating were either distribu
| Recall number | Z-1049-2025 |
|---|---|
| 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 | 2024-12-23 |
| Classified | 2025-01-29 |
| Reported by FDA | 2025-02-05 |
| Distributed | FL, IL, KS, ND, PA, WA, WV |
| Quantity | 50 units |
| Reason classes | labeling, sterility |
| UPC / GTIN / UDI-DI | 10195327561543, 40195327561544 |
| Lot numbers | 24FMF777, 24GMG420, 24IMA276, 24JMI065 |
| Model numbers | DYNJ65208B |
Product
MEDLINE ARTERIAL LINE PACK, REF DYNJ65208B, medical convenience kit containing Infusion Catheter with Antimicrobial Heparin Coating.
Reason for recall
Certain lots Sterile Infusion Catheters which were mislabeled as having a heparin coating were either distributed or manufactured into medical convenience kits and distributed.
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-1049-2025. 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.