Medline CHEST TUBE REORDER NO: DYNJ36762A recalled over sterility concerns
- Recall date
- July 21, 2022
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Medline Industries Inc. recalls Medline CHEST TUBE REORDER NO: DYNJ36762A
- Recall number
- Z-1683-2022
- FDA classification
- Class II
- Brand / firm
- Medline Industries Inc.
- Sold / distributed
- U.S. Nationwide distribution in the state of AL.
Why it was recalled
Due to a non-sterile component (tape) being place within the sterile portion of the Chest Tube Convenience Kit
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Medline CHEST TUBE REORDER NO: DYNJ36762A
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