Recalls · Brand

Sorin Group Italia SRL - CRF recalls

Every recall we track for Sorin Group Italia SRL - CRF — 6 in all, all from 2017 — plus the complaints and injury reports the public filed about them.

6recalls

Recalls per year, by danger level

Recalls from Sorin Group Italia SRL - CRF peaked in 2017 (6); 6 since 2017.

All FDA recall records for Sorin Group Italia SRL - CRF 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.

Recalls per year for Sorin Group Italia SRL - CRF, by danger level
Year	Use caution	Not yet rated	Total
2017	1	5	6
2018	0	0	0
2019	0	0	0
2020	0	0	0
2021	0	0	0
2022	0	0	0
2023	0	0	0
2024	0	0	0
2025	0	0	0
2026 (to date)	0	0	0

What to do if you have a recalled Sorin Group Italia SRL - CRF 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.

See this week’s new recalls.

All Sorin Group Italia SRL - CRF recalls

1 shown

UnratedMedical device
Sorin Group Italia SRL - CRF recalls Platinium VR DF4 1240, Model Number TDF035U, UDI/GTIN 08031527015460, Implantable cardioverter defibrillator,
Sorin Group recalls Platinium VR DF4 1240 ICDs with model TDF035U due to potential overconsumption after electrostatic discharge during surgery or MRI scans. Affected patients should contact manufacturer for guidance.
Sorin GroupJul 24, 2017

Sorin Group Italia SRL - CRF recall questions

How many recalls has Sorin Group Italia SRL - CRF had?

6 recalls from Sorin Group Italia SRL - CRF are on record with U.S. safety agencies, from 2017.

What is the most recent Sorin Group Italia SRL - CRF recall?

Sorin Group Italia SRL - CRF recalls Platinium VR DF4 1240, Model Number TDF035U, UDI/GTIN 08031527015460, Implantable cardioverter defibrillator,, dated Jul 24, 2017. Every Sorin Group Italia SRL - CRF recall is listed on this page, newest first.

What should I do if I have a recalled Sorin Group Italia SRL - CRF 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 Italia SRL - CRF 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.