Class II — Magnolia Medical Technologies, Inc.
| Recalling firm | Magnolia Medical Technologies |
|---|---|
| Registered facility | MAGNOLIA MEDICAL TECHNOLOGIES, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Product was shipped with the incorrect Transfer Adapter Instructions For Use (IFU). |
| 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. |
| Quantity | 9,400 units |
| Distribution | U.S. Nationwide distribution i the states of AL, CO, FL, GA, IL, IN, MD, MI, NE, NY, PA, SC, TX, VA, WV, and WY. O.U.S.: N/A |
| Initiated | 2021-08-02 |
| Classified | 2021-08-31 |
| Terminated | 2023-02-22 |
| Recall number | Z-2393-2021 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Magnolia Medical Technologies, Inc. (Z-2393-2021).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/88338/
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