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

Recall Z-2595-2023 — MEDLINE STERILE IRIS SCISSORS CVD/STD, REF DYNJ04049

U.S. FDA — Device Enforcement · United States · 2023-08-03 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2595-2023
Date of alert
2023-08-03
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
MEDLINE INDUSTRIES, LP - Northfield
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10080196847273
Reported risk: 4.5" Iris Scissors, Sterile, Curved (DYNJ04049) are being recalled due to the potential of the tip protector to fall off. The sharp tip of the scissors could compromise the sterile barrier system by puncturing large and/or small holes that may not be visible to the user.
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.