Arrow International Inc recalls Pneumothorax Kit
- Recall date
- October 24, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1299-2018
- FDA classification
- Class II
- Brand / firm
- Arrow International Inc
- Sold / distributed
- Nationally
Why it was recalled
Product packaging may not be completely sealed.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Pneumothorax Kit
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