LivaNova CP5 Drive Unit Recall: Missing Ferrite Ring Risk

Take action

Contact the company & request your remedy

Recalling firmLivaNova Deutschland GmbHLindberghstr. 25, N/A · Munich, N/A N/A

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

LivaNova is recalling specific CP5 Drive Units used in heart surgery systems due to a possible missing ferrite ring that could cause electrical problems. This affects only certain units with serial numbers starting with 60E03336 to 60E03347.

Why it’s dangerous

The CP5 Drive Unit may have a ferrite ring missing from the power cable, which could lead to electrical interference during heart surgery. This might cause equipment malfunctions but does not pose an immediate danger to patients.

Who’s affected

Heart surgery teams using the specific CP5 Drive Units with serial numbers 60E03336 to 60E03347 are most at risk. These units were sold in the U.S. for use with HLM S5/C5 systems.

How to tell if you have this one

Check if your CP5 Drive Unit has a serial number starting with 60E03336, 60E03339, 60E03344, or 60E03347. These units were used in HLM S5/C5 heart surgery systems.

Brand
LivaNova
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Serial Number
Verify your CP5 Drive Unit's serial number to confirm if it matches the affected range: 60E03336, 60E03339, 60E03344, or 60E03347.

✎ GovInfoNow

Questions people ask

Why is this recall happening?

The recall is due to a possible missing ferrite ring on the power cable, which could cause electrical interference during heart surgery.

Do I need to stop using this device?

No, the recall does not require immediate stoppage. Affected units should be checked for the missing ferrite ring.

How can I confirm if my unit is affected?

Check your CP5 Drive Unit's serial number to see if it starts with 60E03336, 60E03339, 60E03344, or 60E03347.

Take action

Contact LivaNova

We’ve drafted a message you can send LivaNova to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-0787-2022 — LivaNova LivaNova

Hello,

I own a LivaNova that is covered by recall Z-0787-2022 from LivaNova.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

Similar recalls

From people who’ve dealt with this

Experiences, tips, and questions from readers. Every comment is reviewed before it appears.

No comments yet — be the first to share your experience.

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-0787-2022 (December 17, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0787-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

LivaNova Deutschland GmbH recalls Sorin Centrifugal Pump System, CP5, Drive Unit (Catalogue Item #60-01-04, UDI: 04033817900948) used in an HLM S5/C5

Lower-risk recall