Devon Supine — Class II medical device recall Z-1997-2014
Terminated recall by Covidien LLC, reported 2014-07-16, distributed nationwide. Straps may separate from the foam pad.
| Recall number | Z-1997-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Covidien LLC, Mansfield, MA, United States |
| Recall initiated | 2014-05-08 |
| Classified | 2014-07-06 |
| Reported by FDA | 2014-07-16 |
| Terminated | 2015-09-04 |
| Distributed | Nationwide (US) |
| Quantity | 264 devices |
Product
Devon Supine, Lithotomy and Trendelenburg Positioning Kit; Product Code: 31151090 Product Usage: The device is intended to provide padding under the patient, and help maintain the position of an anesthetized patient during surgery.
Reason for recall
Straps may separate from the foam pad.
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-1997-2014. 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.