STOPCOCK EXT — Class II medical device recall Z-2022-2014
Terminated recall by B. Braun Medical, Inc., reported 2014-07-16, distributed nationwide. Complaints were received that reported the stopcock of some Stopcock Extension Sets are assembled in the rever
| Recall number | Z-2022-2014 |
|---|---|
| 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 | 2014-05-29 |
| Classified | 2014-07-08 |
| Reported by FDA | 2014-07-16 |
| Terminated | 2014-12-10 |
| Distributed | Nationwide (US) |
| Quantity | 10,835 |
| Lot numbers | 61356774, 61362114, 61367665 |
Product
STOPCOCK EXT. SET W/ 3-WAY STOPCOCK WITH INJ. SITE AND SPINLOCK CONNECTOR, 22 inches and 37 inches
Reason for recall
Complaints were received that reported the stopcock of some Stopcock Extension Sets are assembled in the reverse position, resulting in the stopcock being closed when set in the open position and vise versa.
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-2022-2014. 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.