Copan Italia recalls BD BBL CultureSwab EZ Collection and Transport System, REF 220144, in vitro Diagnostic, SterileR, Rx Only
- Recall date
- May 2, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1937-2025
- FDA classification
- Class II
- Brand / firm
- Copan Italia
- Sold / distributed
- US Nationwide distribution in the state of MD.
Why it was recalled
Swabs for specimen collection may be prone to breakage during product usage.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
BD BBL CultureSwab EZ Collection and Transport System, REF 220144, in vitro Diagnostic, SterileR, Rx Only
Get recall alerts
Free email alert whenever Copan Italia has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Copan Italia