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

Recall Z-0696-2019 — PROXIMATE¿ PPH Hemorrhoidal Circular Stapler Product Code:PPH03 PPH03: The PROXIMATE¿ PPH Hemorrhoidal Circular Stapler and Accessories have application throughout the anal canal to perform surgical treatment of hemorrhoidal disease

U.S. FDA — Device Enforcement · United States · 2018-12-07 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0696-2019
Date of alert
2018-12-07
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Ethicon Endo-Surgery Inc
Product category
device
Product type
Devices
Reported risk: Hemorrhoidal Circular Stapler may have been assembled without a washer, this may potentially cause bleeding or soft tissue injury during use as the device may not fully cut when fired
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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