Copan Italia Recalls
5 recalls on record · September 11, 2013 to December 24, 2025 · Medical Devices
Recalls by year
13
21
25
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
December 24, 2025Medical DevicesFDA
Copan Italia recalls 1ml of DTT in liquid phase, in PET tube with capture cap, in bulk
Hazard: Treatment reagent functionality in respiratory specimens fluidification cannot be guaranteed.
December 24, 2025Medical DevicesFDA
Copan Italia recalls 1ml of DTT in liquid phase, in PET tube with capture cap, in bulk + sputum transfer device, for WASP* *Compatible wit
Hazard: Treatment reagent functionality in respiratory specimens liquification cannot be guaranteed.
June 18, 2025Medical DevicesFDA
Copan Italia recalls BD BBL CultureSwab EZ Collection and Transport System, REF 220144, in vitro Diagnostic, SterileR, Rx Only
Hazard: Swabs for specimen collection may be prone to breakage during product usage.
September 15, 2021Medical DevicesFDA
Copan Italia recalls COPAN FLOQSwabs, STERILE.EO, for drawing clinical samples. CE0123, for the following reference numbers REF:501CS01,
Hazard: A sterility assurance level of 10-6 cannot be guaranteed due to intentional fraud and data integrity issues at the contract sterilizer, Steril Milano.
September 11, 2013Medical DevicesFDA
Copan Italia recalls WASP (Walk Away Specimen Process). Automatic Planting and Streaking Instrument Catalog number: W086 WASP is a full
Hazard: The recall of the WASP (Walk Away Specimen Process) instrument was initiated because Copan Italia SpA has upgraded the software concerning the broth inoculation table feature. The upgrade has been considered necessary from the manufacturer in order to eliminate the very low risk of rotation of the broth table when the door is open.