Rusch Brochopart and Rusch Brochopart White The Rush Endobronchial… — Class II medical device recall Z-1231-2014
Terminated recall by Teleflex Medical, reported 2014-03-26, distributed nationwide. The product may fail to achieve seal of right lung due to the cuff inflating to one side
| Recall number | Z-1231-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Teleflex Medical, Durham, NC, United States |
| Recall initiated | 2014-02-28 |
| Classified | 2014-03-19 |
| Reported by FDA | 2014-03-26 |
| Terminated | 2016-09-28 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AT, AU, BE, BH, CA, CH, CN, CR, CY, CZ, DE, DK, DO, DZ, EC, EE, EG, ES, FI, FR, GB, GR, GY, HK, HR, HU, IE, IL, IN, IQ, IT, JO, JP, KE, KW, LB, LV, MA, MY, NG, NL, NO, OM, PA, PH, PL, PT, QA, RS, RU, SA, SE, SG, SI, SK, TH, TN, TR, TT, VE |
| Quantity | 63,568 units |
| Reason classes | packaging, device malfunction |
| Lot numbers | 0914M, 0915M, 0917M, 0918M, 0921M, 0922M, 09FE23, 09FE24, 09HE34, 09HE35, 09IE36, 09JE40, 09JE41, 09JE42, 09JE43, 09JE44, 09KE46, 09LE51, 10AE01, 10AE02, 10AE05, 10BE06, 10BE07, 10CE10, 10CE11, 10DE16, 10DE18, 10EE19, 10EE20, 10GE28, 10GE29, 10GE31, 10JE41, 10KE47, 11AE03, 11DE15, 11EE20, 11GE27, 11GE30, 11HE32 and 39 more |
Product
Rusch Brochopart and Rusch Brochopart White The Rush Endobronchial Tube set is indicated for uses commonly associated with oral endobronchial tubes, including, but not limited to, thoracic surgery, bronchospirometry, administration of endobronchial anesthesia, etc. The endobronchial tube allows ventilation and selective inflation or deflation of either lung.
Reason for recall
The product may fail to achieve seal of right lung due to the cuff inflating to one side
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-1231-2014. 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.