PlainRecalls

St. Jude Medical, Cardiac Rhythm Management Division

Compiled from official public sources by the publisher.

14 recalls on record · Latest: Aug 10, 2022

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Agency notice ledger

Federal filing book St. Jude Medical, Cardiac R… LIGHT-BOOK · SINGLE-AGENCY

#1,129 of 14,151 · 14 notices · 0.013% archive

  • BOOK 14 notices
  • RANK #1,129 of 14,151
  • SHARE 0.013% archive
  • AGENCY FDA Devices (14)
  • CAT medical devices
  • CATS 1 category
  • LATEST Aug 10, 2022
  • PHOTO Actavis Elizabeth LLC

Nearest notice-volume peer: Actavis Elizabeth LLC (0 notice gap)

St. Jude Medical, Cardiac Rhythm Management Division accounts for about 0.013% of the 104,423-notice archive on 14 distinct filings — a mid share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Where St. Jude Medical, Cardiac R… sits among 14,151 recalling firms

St. Jude Medical, Cardiac Rhythm Management Division ranks 1,129th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

St. Jude Medical, Cardiac R… vs all firms by recall-notice count

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

14 1129th of 14151 higher than 13,008 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

St. Jude Medical, Cardiac R… in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows St. Jude Medical, Cardiac Rhythm Management Division holds about 0.013% of archive notices alongside 14 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Aug 10, 2022

Merlin 2 PCS MER37000 programmer Model MER3400 software
FDA Devices Moderate Aug 10, 2022

Merlin PCS 3650 programmer Model 3330 software
FDA Devices Moderate Aug 10, 2022

Merlin.net model MN5000 Software
FDA Devices Moderate Apr 27, 2022

Gallant HF Implantable Cardioverter Defibrillator REF# CDHFA500Q
FDA Devices Moderate Apr 27, 2022

Gallant DR Implantable Cardioverter Defibrillator REF # CDDRA500Q
FDA Devices Moderate Apr 27, 2022

Merlin 2 PCS MER3700 programmer Model MER3400 software
FDA Devices Moderate Apr 27, 2022

Merlin PCS 3650 programmer Model 3330 software
FDA Devices Moderate Apr 27, 2022

Gallant VR Implantable Cardioverter Defibrillator REF # CDVRA500Q
FDA Devices Moderate Mar 4, 2020

Ellipse, Tiered-therapy Cardioverter/Defibrillator, REF (UDI/GTIN): CD1377-36QC (05414734507646), CD2411-36C (05414734507585), CD1277-36 (05414734506045), CD1377-36C (05414734507622), CD2277-36Q (05414734505932), CD2377-36QC (05414734507523), with Merlin Patient Care System with software model 3330
FDA Devices Moderate Jan 22, 2020

Merlin PCS Programmer software model 3330, used with Confirm Rx Insertable Cardiac Monitor (ICM), Model DM3500, Sterile. The firm name on the label of the ICM is St. Jude Medical Cardiac Rhythm Management Division, Sylmar, CA. - Product Usage: The Confirm Rx insertable cardiac monitor is designed to detect arrhythmias and wirelessly transmit data to the Merlin.net Patient Care Network. The Confirm Rx ICM is indicated for the monitoring and diagnostic evaluation of patients who experience unexpl
FDA Devices Critical Jan 27, 2016

Optisure Dual Coil Defibrillation Leads, Model No. LDA220, LDA220Q, LDA230Q, LDP220Q. St. Jude Medical. Designed for long term attachment to an Implantable Cardioverter Defibrillator (ICD).
FDA Devices Moderate Sep 23, 2015

Merlin@home RF Remote Monitoring Transmitter Model EX1150. Intended to aid in the remote support of SJM implantable pacemakers and ICD's.
FDA Devices Moderate Jan 21, 2015

Merlin@home RF Remote Monitoring Transmitter, Model EX1150, with software versions 6.1M or 7.0. Usage:RF Remote Transmitter
FDA Devices Moderate Sep 10, 2014

Ellipse Implantable Cardioverter Defibrillators (ICDs), Model No. CD1275, CD1311, CD2275, CD2311, CD1411, CD2411 Ellipse ST Implantable Cardioverter Defibrillators (ICDs), Model No. CD1273, CD1309, CD1409, CD2273, CD2309, CD2409.

St. Jude Medical, Cardiac R… holds a measurable archive slice

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

Similar recall count

Nearest multi-notice firms by distinct-event totals (14 here — thin-book).

Actavis Elizabeth LLC 14 Allergan Sales, LLC 14 American Contract Systems 14 Aurolife Pharma, LLC 14 B&g Foods North America, Inc 14

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

American Contract Systems 14 Bd Switzerland Sarl 14 Biomet Spine, LLC 14 Cardiac Assist, Inc 14

Frequently Asked Questions

How many federal recall notices name St. Jude Medical, Cardiac R…? ▼
PlainRecalls indexes 14 distinct federal recall events naming St. Jude Medical, Cardiac Rhythm Management Division, 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 St. Jude Medical, Cardiac R… sit among other recalling firms? ▼
St. Jude Medical, Cardiac Rhythm Management Division ranks #1,129 of 14,151 by distinct recall-event count among 14,151 firms in this archive (92nd percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of St. Jude Medical, Cardiac R…'s notices? ▼
FDA Devices accounts for 14 of this firm's 14 indexed notices.
What product category dominates St. Jude Medical, Cardiac R…'s filing book? ▼
Filings for St. Jude Medical, Cardiac Rhythm Management Division 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.
St. Jude Medical, Cardiac Rhythm Management Division: 14 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 St. Jude Medical, Cardiac Rhythm Management Division; individual notices remain authoritative on each linked recall page.

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