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

Recall Z-0797-2019 — Henry Schein CU 1000 Halogen Curing Light, Catalog 900-4542. - Product Usage: Curing light for use in dentistry. The labeling did not provide specific details for intended use. Distributed by Henry Schein Inc., Melville, NY.

U.S. FDA — Device Enforcement · United States · 2018-04-04 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0797-2019
Date of alert
2018-04-04
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Handpiece Headquarters
Product category
device
Product type
Devices
Reported risk: Tip of the curing light was too hot causing a heat sensation in the patients.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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