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

Recall Z-2742-2017 — 7245C, 7245C/E, 7245D Computer Digital Video System Product Usage: The 7245C, 7245C/E and 7245D are used to electronically record, display, transfer, and store digital video data of behavior related to swallowing in the pharyngeal area for medical and pedagogical applications.

U.S. FDA — Device Enforcement · United States · 2017-04-13 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2742-2017
Date of alert: 2017-04-13
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Pentax of America Inc
Product category: device
Product type: Devices

Reported risk: Pentax Medical did not always provide transformers with 9175 isolation transformers are used with 7245C, 7245C/E, 7245D, 9200Cs, 9200Ds, 9310HDs, and 9400s computer systems.

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.

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