Steripath Luer Transport Pack — Class II medical device recall Z-2393-2021
Terminated recall by Magnolia Medical Technologies, Inc., reported 2021-09-08, distributed nationwide. Product was shipped with the incorrect Transfer Adapter Instructions For Use (IFU).
| Recall number | Z-2393-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Magnolia Medical Technologies, Inc., Seattle, WA, United States |
| Recall initiated | 2021-08-02 |
| Classified | 2021-08-31 |
| Reported by FDA | 2021-09-08 |
| Terminated | 2023-02-22 |
| Distributed | Nationwide (US) |
| Quantity | 9,400 units |
| Lot numbers | 9448037 |
| Model numbers | 27BD-EN, P00165-000 |
Product
Steripath Luer Transport Pack, Gen2, Luer, BD - Product Usage: This holder/adapter assembly may be used for the access of a specimen from Catheter Port to BD Vacutainer¿ Blood Collection or Urine Collection Tubes.
Reason for recall
Product was shipped with the incorrect Transfer Adapter Instructions For Use (IFU).
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-2393-2021. 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.