Sorin Group USA, Inc. recalls
Every recall we track for Sorin Group USA, Inc. — 24 in all, all from 2017 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Sorin Group USA, Inc. peaked in 2017 (24); 24 since 2017.
All FDA recall records for Sorin Group USA, 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 | 4 | 12 | 8 | 24 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Sorin Group USA, 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 Sorin Group USA, Inc. recalls
4 shown- Use cautionMedical device
Sorin Group USA, Inc. recalls FlexFlow Venous Cannula Model/Catalog Number 200-200 The FlexFlow Venous Cannula is a single use sterile device. It is
Sorin Group recalls FlexFlow Venous Cannula Model 200-200 due to sharper tip than expected. This may cause injury during medical procedures. Affected units have specific lot numbers.
Sorin GroupSep 28, 2017 - Use cautionMedical device
Sorin Group USA, Inc. recalls STOCKERT Heater-Cooler System 3T, 120V/60 Hz
Sorin Group recalls STOCKERT Heater-Cooler System 3T models with potential hydrogen peroxide diffusion risk. Affected units have specific serial numbers and item numbers. Contact for remedy details.
Sorin GroupJun 30, 2017 - Lower riskMedical device
Sorin Group USA, Inc. recalls SORIN GROUP, SMART PERFUSION PACK, SMART 1/4" PEDS PACK, REF 627262502, STERILE EO, Rx Only, 1 EA
Sorin Group recalls SMART Perfusion Packs with potential sterile barrier breaches due to small pinholes in packaging. Affected units include specific lot numbers.
Sorin GroupJun 29, 2017 - Lower riskMedical device
Sorin Group USA, Inc. recalls Sorin Group Aortic Arch Cannula, 7 mm x 10 in x 3/8 in, Rx Only, Sterile Product Usage: The Aortic Arch Cannulae are
Sorin Group recalls specific aortic arch cannulas due to excess plastic on the tip. This may cause issues during surgery. Affected models and lots are listed in the recall notice.
Sorin GroupJun 9, 2017
Sorin Group USA, Inc. recall questions
How many recalls has Sorin Group USA, Inc. had?
24 recalls from Sorin Group USA, Inc. are on record with U.S. safety agencies, from 2017.
What is the most recent Sorin Group USA, Inc. recall?
Sorin Group USA, Inc. recalls FlexFlow Venous Cannula Model/Catalog Number 200-200 The FlexFlow Venous Cannula is a single use sterile device. It is, dated Sep 28, 2017. Every Sorin Group USA, Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Sorin Group USA, 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 Sorin Group USA, 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.