BD PrecisionGlide Needle 30G x 1/2 — Class II medical device recall Z-0588-2021
Terminated recall by Becton Dickinson & Company, reported 2020-12-23, distributed nationwide. BD has confirmed the presence of blood on the cannulas of the BD PrecisionGlide needles 30G X 1/2" Lot No. 912
| Recall number | Z-0588-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Becton Dickinson & Company, Franklin Lakes, NJ, United States |
| Recall initiated | 2020-11-18 |
| Classified | 2020-12-15 |
| Reported by FDA | 2020-12-23 |
| Terminated | 2024-02-15 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, CN, SG |
| Quantity | 1,430,000 |
| UPC / GTIN / UDI-DI | 30382903051060 |
| Lot numbers | 9128897 |
| Model numbers | 305106 |
| Expiration dates | 2024-06-30 |
Product
BD PrecisionGlide Needle 30G x 1/2 (0.3 mm X 13mm) REF 305106 - Product Usage: used for general purpose injection and aspiration of fluids from vials, ampoules and parts of the body below the surface of the skin.
Reason for recall
BD has confirmed the presence of blood on the cannulas of the BD PrecisionGlide needles 30G X 1/2" Lot No. 9128897. The possibility of infection may be present if the blood is not noticed prior to use by the clinician.
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-0588-2021. 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.