Stryker GmbH recalls Endotrac ECTR Hook/Triangle Blade Kit, Catalogue Number 2056-1
- Recall date
- April 30, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1848-2019
- FDA classification
- Class II
- Brand / firm
- Stryker GmbH
- Sold / distributed
- The products were distributed US nationwide.
Why it was recalled
The seal integrity of the sterile bag containing the kits may be compromised.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Endotrac ECTR Hook/Triangle Blade Kit, Catalogue Number 2056-1
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