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

Recall Z-1936-2017 — AL-III-DISS Adapter Product Usage: Pneumatic system

U.S. FDA — Device Enforcement · United States · 2016-10-06 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1936-2017
Date of alert
2016-10-06
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
The Anspach Effort, Inc.
Product category
device
Product type
Devices
Reported risk: Supplied Directions for Use (DFU) did not contain a recommended service interval.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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