Bronchial Double Lumen Tube Set — Class II medical device recall Z-2408-2015
Terminated recall by Teleflex, Inc., reported 2015-08-26, distributed in AK, AL, AZ, CA, CO, CT, DC, DE…. Customer complaints reporting that the cobb connector detached from the main connector prior to use.
| Recall number | Z-2408-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Teleflex, Inc., Wayne, PA, United States |
| Recall initiated | 2014-11-21 |
| Classified | 2015-08-19 |
| Reported by FDA | 2015-08-26 |
| Terminated | 2017-08-15 |
| Distributed | AK, AL, AZ, CA, CO, CT, DC, DE, FL, GA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MO, MS, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, PR, SC, TN, TX, UT, VA, WA, WI, WV |
| Countries outside the US | BO, CA, EC, HK, MY, PH, TT, TW |
| Reason classes | device malfunction |
| Lot numbers | 13FT06, 13FT12, 13FT12R, 13FT17, 13FT18, 13GE28J, 13GE29J, 13GE30J, 13GT05, 13GT11, 13GT16, 13GT23, 13GT24, 13GT29, 13HT07, 13HT12, 13HT17, 13IT05, 13IT10, 13IT13, 13IT16, 13IT20, 13IT20R, 13JT05, 13JT05R, 13JT08, 13JT11, 13JT15, 13JT20, 13JT20R, 13JT21, 13KT05, 13KT12, 13KT18, 13KT23, 13LT04, 13LT08, 13LT11, 13LT14, 14AT04 and 52 more |
Product
Bronchial Double Lumen Tube Set (Right), Sterile
Reason for recall
Customer complaints reporting that the cobb connector detached from the main connector prior to use.
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-2408-2015. 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.