Copan Italia: Device Recall
Recall #Z-1937-2025 · 05/02/2025
Class II: Risk
Recall Details
- Recall Number
- Z-1937-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Copan Italia
- Status
- Ongoing
- Date Initiated
- 05/02/2025
- Location
- Brescia, Italy
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 81,600 units
Reason for Recall
Swabs for specimen collection may be prone to breakage during product usage.
Product Description
BD BBL CultureSwab EZ Collection and Transport System, REF 220144, in vitro Diagnostic, SterileR, Rx Only
Distribution Pattern
US Nationwide distribution in the state of MD.
Other Recalls by Copan Italia
- Class II: Risk 10/29/2025
- Class II: Risk 10/29/2025
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.