Jamshidi Bone Marrow Biopsy/Aspiration Needle — Class II medical device recall Z-1689-2020
Terminated recall by Bard Peripheral Vascular Inc, reported 2020-04-15, distributed nationwide. Sterility compromised due to packaging pouches that may not be sealed properly
| Recall number | Z-1689-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Bard Peripheral Vascular Inc, Tempe, AZ, United States |
| Recall initiated | 2020-03-17 |
| Classified | 2020-04-09 |
| Reported by FDA | 2020-04-15 |
| Terminated | 2024-07-15 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, IN, JP, MY, NZ, PH, SG |
| Reason classes | sterility |
| Lot numbers | 0001303256, 0001303257 |
Product
Jamshidi Bone Marrow Biopsy/Aspiration Needle, with Luer Lock Adapter 11GX4 ASP, Sterile - Product Code: DJ4011X - Product Usage: The device is comprised of an outer cannula with a handle and an inner stylet. Its intended use is for the posterior iliac crest biopsy technique.
Reason for recall
Sterility compromised due to packaging pouches that may not be sealed properly
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-1689-2020. 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.