PE CONNECTOR 5 IN 1 20/BX — Class II medical device recall Z-2129-2017
Terminated recall by Teleflex Medical, reported 2017-05-31, distributed nationwide. Labeling: The expiration date is not stated on the labeling, there is a potential for expired product to be us
| Recall number | Z-2129-2017 |
|---|---|
| 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 |
| Reason classes | labeling |
| Lot numbers | 02A1101041, 02B1102552, 02C1001258, 02C1003795, 02C1101253, 02C1104114, 02D0802670, 02D0803968, 02D1000682, 02D1002136, 02D1101334, 02E1001502, 02E1100384, 02F0800281, 02F1000667, 02F1002368, 02F1101766, 02F1102607, 02F1103754, 02G1000322, 02G1001538, 02H0801670, 02H0803375, 02H1000732, 02H1103023, 02H1103940, 02J1000236, 02J1001515, 02J1002609, 02J1003237, 02J1101139, 02J1102143, 02K1000270, 02K1001993, 02K1100519, 02K1103124, 02K1301613, 02L0701463, 02L0701958, 02L0702675 and 16 more |
Product
PE CONNECTOR 5 IN 1 20/BX, Sterile, Single use, Product Usage: Catheter Connector/Accessory
Reason for recall
Labeling: The expiration date is not stated on the labeling, there is a potential for expired product to be used.
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-2129-2017. 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.