REF TIN3015 — Class II medical device recall Z-0002-2022
Ongoing recall by Bard Peripheral Vascular Inc, reported 2021-10-13, distributed nationwide. Potential for needle protector to become fully dislodge exposing infusion needle which could result in needle
| Recall number | Z-0002-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Bard Peripheral Vascular Inc, Tempe, AZ, United States |
| Recall initiated | 2021-07-27 |
| Classified | 2021-10-01 |
| Reported by FDA | 2021-10-13 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AU, BE, CA, CN, HK, IN, JP, MX, MY, NL, NZ, SG, TW, VN, ZA |
| UPC / GTIN / UDI-DI | 10885403043796 |
| Serial numbers | 1000061, 1004858, 1005204, 1007650, 1010791, 1013939, 1017379, 1035580, 1035581, 1038740, 1044131, 1049259, 1050881, 1052628, 1057742, 1059045, 1061515, 1065338, 1066413, 1066484, 1068754, 1069385, 1072036, 1072932, 1076214 and 216 more |
| Model numbers | TIN3015 |
Product
REF TIN3015, 15G x 79 mm Bone Marrow Aspiration/Intraosseous Infusion Needle, For Single Use Only, Sterile EO, UDI: 10885403043796
Reason for recall
Potential for needle protector to become fully dislodge exposing infusion needle which could result in needle stick.
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-0002-2022. 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.