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

Recall Z-0097-2024 — NOVAPLUS GAMMEX NON-LATEX PI GREEN Surgical gloves, REF: V20685255 through V20685290

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-0097-2024
Date of alert
2023-08-03
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Ansell Healthcare Products LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
2203434604
Reported risk: Some surgical glove sterile pouches were not completely sealed.
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.

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