Pluer-evac Sahara Chest Drainage System — Class II medical device recall Z-1404-2015
Terminated recall by Teleflex Medical, reported 2015-04-15, distributed in AK, AL, AR, CA, CO, FL, GA, IL…. Package contains incorrect sized unit: The adult sized S-1100-08LF product contains an infant sized chest drai
| Recall number | Z-1404-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Teleflex Medical, Research Triangle Park, NC, United States |
| Recall initiated | 2015-03-13 |
| Classified | 2015-04-08 |
| Reported by FDA | 2015-04-15 |
| Terminated | 2017-08-14 |
| Distributed | AK, AL, AR, CA, CO, FL, GA, IL, IN, KS, KY, MA, MD, MI, MN, NY, OH, PA, RI, SC, TX, VA, WI, WV |
| Quantity | 2,148 units |
| Lot numbers | 74F1400878 |
| Model numbers | S-1100-08LF |
Product
Pluer-evac Sahara Chest Drainage System, S-1100-08LF, Dry Suction/Dry Seal Control, Rx Only, Teleflex Medical.
Reason for recall
Package contains incorrect sized unit: The adult sized S-1100-08LF product contains an infant sized chest drainage system.
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-1404-2015. 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.