The Anspach Effort, Inc. recalls IMRI CRANI-A ATTACHMENT Product Usage: Pneumatic system
- Recall date
- October 6, 2016
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1996-2017
- 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
IMRI CRANI-A ATTACHMENT Product Usage: Pneumatic system
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