FDA Device recall Z-2415-2015
Bronchial Double Lumen Tube Set (Left), Extra Length, Sterile
- FDA Device
- Class II
- terminated
- Published 2015-08-26
On 2015-08-26 the FDA classified a Class II recall of Bronchial Double Lumen Tube Set (Left), Extra Length, Sterile by Teleflex, citing customer complaints reporting that the cobb connector detached from the main connector prior to use.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2415-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-11-21 |
| Published | 2015-08-26 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Teleflex |
| Distribution | 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 |
Product
Bronchial Double Lumen Tube Set (Left), Extra Length, Sterile
Reason
Customer complaints reporting that the cobb connector detached from the main connector prior to use.
Identifiers
| code_info | Product Code 116164-000390 Batch Number 14BT21 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2415-2015%22
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