St. Jude Medical, Cardiac Rhythm Management Division
10 recalls on record · Latest: Aug 10, 2022
St. Jude Medical, Cardiac Rhythm Management Division Recall Insight
St. Jude Medical, Cardiac Rhythm Management Division appears on 10 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.012% of the federal archive — a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Aug 10, 2022, which is the anchor point for assessing whether enforcement is currently active or historical.
On this page of 10 entries, severity tagging shows 1 critical, 9 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 10 of 10 entries — unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (10). The date window on this page runs from Jan 21, 2015 to Aug 10, 2022.
Manufacturer-level browsing is useful when monitoring a single firm for patterns — whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current — deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement — always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.
Merlin 2 PCS MER37000 programmer Model MER3400 software
Merlin PCS 3650 programmer Model 3330 software
Merlin.net model MN5000 Software
Gallant HF Implantable Cardioverter Defibrillator REF# CDHFA500Q
Gallant DR Implantable Cardioverter Defibrillator REF # CDDRA500Q
Ellipse, Tiered-therapy Cardioverter/Defibrillator, REF (UDI/GTIN): CD1377-36QC (05414734507646), CD2411-36C (05414734507585), CD1277-36 (05414734506…
Merlin PCS Programmer software model 3330, used with Confirm Rx Insertable Cardiac Monitor (ICM), Model DM3500, Sterile. The firm name on the label …
Optisure Dual Coil Defibrillation Leads, Model No. LDA220, LDA220Q, LDA230Q, LDP220Q. St. Jude Medical. Designed for long term a…
Merlin@home RF Remote Monitoring Transmitter Model EX1150. Intended to aid in the remote support of SJM implantable pacemakers and ICD's.
Merlin@home RF Remote Monitoring Transmitter, Model EX1150, with software versions 6.1M or 7.0. Usage:RF Remote Transmitter
Nearby Manufacturers
Other firms with recall activity tracked in the PlainRecalls index.
FORD
View recalls →
Newly Weds Foods Inc
View recalls →
Zimmer Biomet, Inc.
View recalls →
Garden-Fresh Foods, Inc.
View recalls →
Aidapak Services, LLC
View recalls →
Compare St. Jude Medical, Cardiac Rhythm Management Division with FORD →
Data Sources
Explore Related Data
Read our methodology — how this data is sourced, computed, and verified.