Teleflex Medical RUSCH Pocket Pac i — Class II medical device recall Z-0227-2023
Ongoing recall by TELEFLEX LLC, reported 2022-11-23, distributed in CA, FL, IL, MO, NC, OH, OR, TN…. Product may not be sterile
| Recall number | Z-0227-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | TELEFLEX LLC, Morrisville, NC, United States |
| Recall initiated | 2022-09-20 |
| Classified | 2022-11-11 |
| Reported by FDA | 2022-11-23 |
| Distributed | CA, FL, IL, MO, NC, OH, OR, TN, TX |
| Quantity | 7,200 catheters |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 24026704323245 |
| Model numbers | 10096140 |
Product
Teleflex Medical RUSCH Pocket Pac i.c. Closed System Intermittent Catheter Kit, 14 Fr (4.7mm), REF 10096140 (IPN050116). Urinary catheter.
Reason for recall
Product may not be sterile
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-0227-2023. 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.