Medical device recalls Moderate risk

The Anspach Effort, Inc. recalls 90 degree Contra Angle Attachment Product Usage: Pneumatic system

Recall date
October 6, 2016
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-2018-2017
FDA classification
Class II
Brand / firm
The Anspach Effort, Inc.
Sold / distributed
Worldwide Distribution - US Nationwide in the states of HI, DC including PR and the countries of Guam and Japan

Why it was recalled

Supplied Directions for Use (DFU) did not contain a recommended service interval.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

90 degree Contra Angle Attachment Product Usage: Pneumatic system

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