PE CONNECTOR 3/8 STRAIGHT 20/BX — Class II medical device recall Z-2127-2017
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-2127-2017 |
|---|---|
| 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 | 02F0801115, 02F0901859, 02G0802748, 02G0900814, 02H0900192, 02K0900567, 02L0900163, 02M0901006, 74A1601695, 74G1500137, 74G1502714, 74M1400489 |
Product
PE CONNECTOR 3/8 STRAIGHT 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-2127-2017. 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.