FDA Device recall Z-1692-2023
Sterile custom surgical procedure packs (1) 89-10529.04, CNRV OR C-SECTION PACK, New River Valley Medical Center
- FDA Device
- Class II
- ongoing
- Published 2023-06-14
On 2023-06-14 the FDA classified a Class II recall of Sterile custom surgical procedure packs (1) 89-10529.04, CNRV OR C-SECTION PACK, New River Valley Medical Center by Deroyal Industries, citing the custom procedure packs contain light handle covers that have been recalled by another firm.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1692-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-04-17 |
| Published | 2023-06-14 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Deroyal Industries |
| Distribution | US |
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
The custom procedure packs contain light handle covers that have been recalled by another firm.
Identifiers
| code_info | (1) 89-10529.04 - lot 58700691, exp 11/1/2024, GTIN pack-00749756363334, case-50749756363339; (2) 89-10567.05 - lot 587…(1) 89-10529.04 - lot 58700691, exp 11/1/2024, GTIN pack-00749756363334, case-50749756363339; (2) 89-10567.05 - lot 58700026, exp 12/1/2024, GTIN pack-00749756364300, case-50749756364305. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Other recalls by Deroyal Industries
- REF: 81-030415 Myocardial Probe Non-Pyrogenic , 400 Series
FDA Device · Class II · 2026-09-30 · Deroyal Industries - DeRoyal Industries Inc
FDA Device · Class II · 2026-06-10 · Deroyal Industries - DeRoyal REF 71-C5100NS Tubing, Suction, Connector
FDA Device · Class II · 2025-03-12 · Deroyal Industries - DeRoyal AMG Suction Connector Tubing REF: 71-2083, 71-C506, 71-C510, 71-C512, 71-C520, Tubing is intended for fluid movement
FDA Device · Class II · 2025-02-26 · Deroyal Industries - DeRoyal CHILDREN'S LAPTRACEPACK, 89-9362.06
FDA Device · Class II · 2024-11-13 · Deroyal Industries
All Deroyal Industries recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1692-2023%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.