Diasorin Inc. recalls
Every recall we track for Diasorin Inc. — 4 in all, from 2020–2024 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
4 recalls since 2017.
All FDA recall records for Diasorin Inc. 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 | 2 | 0 | 2 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 1 | 0 | 1 |
| 2024 | 0 | 0 | 1 | 0 | 1 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Diasorin Inc. 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 Diasorin Inc. recalls
4 shown- Lower riskMedical device
Diasorin Inc. recalls DiaSorin LIAISON Q.S.E.T. Device Plus, REF 319060; intended for use in the preparation of human stool specimens
Diasorin recalls LIAISON Q.S.E.T. Device Plus (REF 319060) due to loose caps causing buffer leaks. This may lead to incorrect stool test results. Affected units include specific lot numbers for stool specimen preparation.
DiasorinNov 7, 2024 - Lower riskMedical device
Diasorin Inc. recalls DiaSorin LIAISON HSV-2 Type Specific IgG, REF 310620
Diasorin recalls specific lots of HSV-2 Type Specific IgG test kits that may produce false positive results. Affected lots include 136344 through 136775. No action needed for users but verify your lot number.
DiasorinDec 13, 2023 - Lower riskMedical device
Diasorin Inc. recalls LIAISON 1-84 PTH Assay - Product Usage: is an in vitro chemiluminescent immunoassay (CLIA) intended for the
Diasorin recalls LIAISON 1-84 PTH Assay kits with potential for false high parathyroid hormone results. Affected lots: 134909, 134909A, 134909B. Contact for remedy.
Diasor: LIAISONNov 23, 2020 - Lower riskMedical device
Diasorin Inc. recalls Parvovirus B19 IgG EIA kit Part No. V519IGUS
Diasorin recalls Parvovirus B19 IgG EIA kit (Part No. V519IGUS) due to incorrect label value. This may affect test accuracy. No remedy specified in recall notice.
Diasor:inJul 17, 2020
Diasorin Inc. recall questions
How many recalls has Diasorin Inc. had?
4 recalls from Diasorin Inc. are on record with U.S. safety agencies, from 2020–2024.
What is the most recent Diasorin Inc. recall?
Diasorin Inc. recalls DiaSorin LIAISON Q.S.E.T. Device Plus, REF 319060; intended for use in the preparation of human stool specimens, dated Nov 7, 2024. Every Diasorin Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Diasorin Inc. 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 Diasorin Inc. 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.