LeMaitre Vascular, Inc. recalls LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter (eIFU) REF# e2400-51
- Recall date
- February 7, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1443-2017
- FDA classification
- Class II
- Brand / firm
- LeMaitre Vascular, Inc.
- Sold / distributed
- Worldwide distribution. US Nationwide, AUSTRIA, BELGIUM, FRANCE, GERMANY, ITALY, LUXEMBOURG, Morocco, Saudi Arabia, Singapore, SPAIN, SWITZERLAND, UAE, and UK
Why it was recalled
The Contains Latex symbol was not printed onto the box label or the sterile (inner) product pouch
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter (eIFU) REF# e2400-51
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