PleuraGuide Disposable Chest Tube Kit — Class II medical device recall Z-1987-2013
Terminated recall by Atrium Medical Corporation, reported 2013-08-28, distributed nationwide. Individual component's IFUs are not included with the kit.
| Recall number | Z-1987-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Atrium Medical Corporation, Hudson, NH, United States |
| Recall initiated | 2013-07-16 |
| Classified | 2013-08-20 |
| Reported by FDA | 2013-08-28 |
| Terminated | 2014-07-15 |
| Distributed | Nationwide (US) |
| Quantity | 6,516 units |
| Model numbers | 10728234, 10728235, 10728236, 10728237, 10728238, 10728239, 10734583, 10734584, 10734585, 10734588, 10734589, 10734590, 10736238, 10736242, 10736243, 10736244, 10736245, 10794372, 10800926, 10802725, 10802727, 10820803, 10823084, 10825183, 10827874 and 46 more |
Product
PleuraGuide Disposable Chest Tube Kit; Product codes: 17100, 17150, and 17200. Indicated to assist with the insertion of thoracic catheters.
Reason for recall
Individual component's IFUs are not included with the kit.
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-1987-2013. 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.