PlainRecalls

LivaNova Deutschland GmbH

Compiled from official public sources by the publisher.

5 recalls on record · Latest: Dec 4, 2024

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Agency notice ledger

Federal filing book LivaNova Deutschland GmbH LIGHT-BOOK · SINGLE-AGENCY

#2,540 of 14,151 · 5 notices · 0.005% archive

  • BOOK 5 notices
  • RANK #2,540 of 14,151
  • SHARE 0.005% archive
  • AGENCY FDA Devices (5)
  • CAT medical devices
  • CATS 1 category
  • LATEST Dec 4, 2024
  • PHOTO A G Specialty Foods I…

Nearest notice-volume peer: A G Specialty Foods Inc (0 notice gap)

LivaNova Deutschland GmbH accounts for about 0.005% of the 104,423-notice archive on 5 distinct filings — a light share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

How LivaNova Deutschland GmbH compares to 14,151 recalling firms

LivaNova Deutschland GmbH ranks 2,540th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

LivaNova Deutschland GmbH vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

5 2540th of 14151 higher than 11,411 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13

LivaNova Deutschland GmbH in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows LivaNova Deutschland GmbH holds about 0.005% of archive notices alongside 5 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Dec 4, 2024

Essenz HLM (Heart-Lung Machine), REF: 49-00-10, with Software
FDA Devices Moderate Oct 18, 2023

3T Heater Cooler System, REF: 16-02-85
FDA Devices Low Mar 23, 2022

Sorin Centrifugal Pump System, CP5, Drive Unit (Catalogue Item #60-01-04, UDI: 04033817900948) used in an HLM S5/C5 System configuration. A cardiopulmonary bypass speed control device.
FDA Devices Moderate Jul 8, 2020

Control Panel REF - 60-02-15: LivaNova SCP Pump Control Panel. REF 60-02-15, IPX2, RxOnly, UDI: 04033817900986
FDA Devices Moderate Jul 8, 2020

Control Panel REF - 60-02-50: LivaNova SCP Pump Control Panel S5/C5. REF 60-02-50, IPX2, RxOnly, UDI: 04033817900993

LivaNova Deutschland GmbH is a small archive contributor

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Frequently Asked Questions

How many federal recall notices name LivaNova Deutschland GmbH? ▼
PlainRecalls indexes 5 distinct federal recall events naming LivaNova Deutschland GmbH, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does LivaNova Deutschland GmbH sit among other recalling firms? ▼
LivaNova Deutschland GmbH ranks #2,540 of 14,151 by distinct recall-event count among 14,151 firms in this archive (81st percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of LivaNova Deutschland GmbH's notices? ▼
FDA Devices accounts for 5 of this firm's 5 indexed notices.
What product category dominates LivaNova Deutschland GmbH's filing book? ▼
Filings for LivaNova Deutschland GmbH span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
LivaNova Deutschland GmbH: 5 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming LivaNova Deutschland GmbH; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026