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

Recall Z-1991-2023 — Metal Tray, 178 x 135 x 37 mm, REF: 11580A; Metal Tray, 275 x 178 x 35 mm, REF: 11580B; Metal Tray, 373 x 178 x 35 mm, REF: 11580C; Metal Tray, 275 x 175 x 37 mm, REF: 11580D; Wire Tray f. Cleaning, 290x60x52mm, REF: 39501A1; Wire Tray f. Cleaning, 352 x 125 x 54 mm, REF: 39501A2; Wire Tray f.

U.S. FDA — Device Enforcement · United States · 2023-04-06 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1991-2023
Date of alert
2023-04-06
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Karl Storz Endoscopy
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
04048551051801
Reported risk: Metal sterilization trays used to encase and protect medical devices during sterilization have a new 510(k) with instructions for use that is for the first time specific to the tray models, that also includes information regarding the sterilization modality.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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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.