BD Precision Glide Needle 18G x 1 RB — Class II medical device recall Z-0207-2018
Terminated recall by Becton Dickinson & Company, reported 2017-12-13, distributed nationwide. Hub damage resulting in breakage and/or leakage during use.
| Recall number | Z-0207-2018 |
|---|---|
| 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 | 2017-05-31 |
| Classified | 2017-12-07 |
| Reported by FDA | 2017-12-13 |
| Terminated | 2018-06-28 |
| Distributed | Nationwide (US) |
| Quantity | 2,598,000 units |
| Reason classes | packaging, device malfunction |
| Lot numbers | 6152995 |
| Model numbers | 305195 |
| Expiration dates | 2021-07-31 |
Product
BD Precision Glide Needle 18G x 1 RB, Catalog 305195 Product Usage: These needles are intended for general purpose fluid injection/aspiration, infusion, venipuncture to obtain blood collection and insulin injection.
Reason for recall
Hub damage resulting in breakage and/or leakage during use.
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-0207-2018. 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.