Sterile custom surgical procedure packs — Class II medical device recall Z-1692-2023
Ongoing recall by DeRoyal Industries Inc, reported 2023-06-14, distributed nationwide. The custom procedure packs contain light handle covers that have been recalled by another firm.
| Recall number | Z-1692-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | DeRoyal Industries Inc, Powell, TN, United States |
| Recall initiated | 2023-04-17 |
| Classified | 2023-06-07 |
| Reported by FDA | 2023-06-14 |
| Distributed | Nationwide (US) |
| Lot numbers | 58700026, 58700691 |
| Expiration dates | 2024-11-01, 2024-12-01 |
Product
Sterile custom surgical procedure packs (1) 89-10529.04, CNRV OR C-SECTION PACK, New River Valley Medical Center; and (2) 89-10567.05, OB-OR C-SECTION PACK, Carilion Roanoke Memorial Hospital.
Reason for recall
The custom procedure packs contain light handle covers that have been recalled by another firm.
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-1692-2023. 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.