Class II

Medical Device Recall: BD BBL CultureSwab EZ Collection and Transport System, REF 220144, in vitro Diagnostic, SterileR, Rx Only

Copan Italia · May 2, 2025

Reason for Recall

Swabs for specimen collection may be prone to breakage during product usage.

Distribution

US Nationwide distribution in the state of MD.

States Affected

NATIONWIDE

Quantity Affected

81,600 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1937-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Copan Italia Medical Device Recall: BD BBL CultureSwab EZ Collection and Transport System, REF 220144, in vitro Diagnostic, SterileR, Rx Only | SafeCheck