Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1691-2023 — Sterile custom surgical procedure packs: (1) 89-10507.02, TOTAL KNEE PACK, Stonewall Jackson Hospital; (2) 89-10508.02, LOCAL PACK, Stonewall Jackson Hospital; (3) 89-10509.02, LAPAROTOMY PACK, Stonewall Jackson Hospital; (4) 89-10517.04, CNRV BASIC SETUP PACK, New River Valley Medical Center;

U.S. FDA — Device Enforcement · United States · 2023-04-17 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1691-2023
Date of alert: 2023-04-17
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: DeRoyal Industries Inc
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 58700464

Reported risk: The custom procedure packs contain light handle covers that have been recalled by another firm.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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