INFANT 20/BX — Class II medical device recall Z-2130-2017
Terminated recall by Teleflex Medical, reported 2017-05-31, distributed nationwide.
| Recall number | Z-2130-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Teleflex Medical, Research Triangle Park, NC, United States |
| Recall initiated | 2017-04-21 |
| Classified | 2017-05-22 |
| Reported by FDA | 2017-05-31 |
| Terminated | 2020-01-27 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, CN, IN, KR, SG |
| Quantity | 19,043 units |
| Lot numbers | 02B1300991, 02B1402029, 02C1301654, 02E1201155, 02H1302224, 02K1100520, 02K1103125, 02K1200732, 02K1202185, 02L0701465, 02L0701959, 02L1201668, 02L1203112, 02M1201149, 74A1601005, 74F1400876.74H1601152, 74J1601641, 74K1501590, 74L1500555 |
Product
INFANT 20/BX, Sterile, Single use Product Usage: Catheter Connector/Accessory
Reason for recall
Not stated by FDA.
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-2130-2017. 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.