FDA Device recall Z-1404-2015
Pluer-evac Sahara Chest Drainage System, S-1100-08LF, Dry Suction/Dry Seal Control, Rx Only, Teleflex Medical
- FDA Device
- Class II
- terminated
- Published 2015-04-15
On 2015-04-15 the FDA classified a Class II recall of Pluer-evac Sahara Chest Drainage System, S-1100-08LF, Dry Suction/Dry Seal Control, Rx Only, Teleflex Medical by Teleflex Medical, citing package contains incorrect sized unit: The adult sized S-1100-08LF product contains an infant sized chest drainage system.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1404-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-03-13 |
| Published | 2015-04-15 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Teleflex Medical |
| Distribution | AK, AL, AR, CA, CO, FL, GA, IL, IN, KS, KY, MA, MD, MI, MN, NY, OH, PA, RI, SC, TX, VA, WI, WV |
Product
Pluer-evac Sahara Chest Drainage System, S-1100-08LF, Dry Suction/Dry Seal Control, Rx Only, Teleflex Medical.
Reason
Package contains incorrect sized unit: The adult sized S-1100-08LF product contains an infant sized chest drainage system.
Identifiers
| code_info | Catalogue no. S-1100-08LF, Lot no. 74F1400878 |
|---|
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-1404-2015%22
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