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

Recall Z-1872-2013 — Non-sterile Viscot Surgical Skin Markers Part Number 1437-100 Non-sterile Viscot Part Number 143-100 Surgical Skin Markers are pen-like devices intended to be used to write on the patient's skin, e.g., to outline surgical incision sites or mark anatomical sites for accurate blood pressure mea

U.S. FDA — Device Enforcement · United States · 2013-07-10 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1872-2013
Date of alert: 2013-07-10
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Precision Dynamics Corporation
Product category: device
Product type: Devices

Reported risk: PDC Healthcare initiated this recall of Non-Sterile Viscot Part Number 1437-100 Surgical Skin Markers, becuase they were inadvertently mislabeled as PN STER-VIS Sterile Skin Marker Pen with Labels and Flex Ruter.

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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