Copan Italia recalls
Every recall we track for Copan Italia — 4 in all, from 2021–2025 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Copan Italia peaked in 2025 (3); 4 since 2017.
All FDA recall records for Copan Italia since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 1 | 0 | 1 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 3 | 0 | 3 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Copan Italia product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Copan Italia recalls
3 shown- Lower riskMedical device
Copan Italia recalls 1ml of DTT in liquid phase, in PET tube with capture cap, in bulk + sputum transfer device, for WASP* *Compatible with
Copan Italia recalls 1ml DTT liquid reagent for WASP systems due to uncertain respiratory specimen liquification. Affected units include PET tubes with capture caps sold with sputum transfer devices.
Copan ItaliaOct 29, 2025 - Lower riskMedical device
Copan Italia recalls BD BBL CultureSwab EZ Collection and Transport System, REF 220144, in vitro Diagnostic, SterileR, Rx Only
Copan Italia recalls BD BBL CultureSwab EZ Collection and Transport System (REF 220144) due to risk of swab breakage during specimen collection. This in vitro diagnostic product requires immediate attention for safety.
Copan ItaliaMay 2, 2025 - Lower riskMedical device
Copan Italia recalls COPAN FLOQSwabs, STERILE.EO, for drawing clinical samples. CE0123, for the following reference numbers REF:501CS01,
Copan recalls FLOQSwabs and STERILE.EO swabs due to sterility assurance failures from a contract sterilizer. These swabs may not be sterile, risking infections during clinical sampling.
CopanJul 9, 2021
Copan Italia recall questions
How many recalls has Copan Italia had?
4 recalls from Copan Italia are on record with U.S. safety agencies, from 2021–2025.
What is the most recent Copan Italia recall?
Copan Italia recalls 1ml of DTT in liquid phase, in PET tube with capture cap, in bulk + sputum transfer device, for WASP* *Compatible with, dated Oct 29, 2025. Every Copan Italia recall is listed on this page, newest first.
What should I do if I have a recalled Copan Italia product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Copan Italia recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.