CNB200T CONTIPLEX TUOHY SET 2 IN — Class II medical device recall Z-3317-2018
Terminated recall by B. Braun Medical, Inc., reported 2018-10-10, distributed nationwide. The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the cathe
| Recall number | Z-3317-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | B. Braun Medical, Inc., Allentown, PA, United States |
| Recall initiated | 2018-07-20 |
| Classified | 2018-10-01 |
| Reported by FDA | 2018-10-10 |
| Terminated | 2020-05-13 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, GT, KW |
| Quantity | 5,460 |
| Reason classes | packaging |
| Lot numbers | 61598571, 61605368 |
Product
CNB200T CONTIPLEX TUOHY SET 2 IN, Material Number 331691 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction with the catheter for continuous administration of anesthetic fluids.
Reason for recall
The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been observed.
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-3317-2018. 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.