Device manufacturer, as written on reports

St Jude Medical Puerto Rico: medical device reports filed with FDA

2,351 reports name it as the manufacturer of the device involved, 1997–2022.

Read first · FDA's statement on these data

Adverse event reports submitted to FDA do not undergo extensive validation or verification. Therefore, a causal relationship cannot be established between product and reactions listed in a report. While a suspected relationship may exist, it is not medically validated and should not be the sole source of information for clinical decision making or other assumptions about the safety or efficacy of a product. Additionally, it is important to remember that adverse event reports represent a small percentage of total usage numbers of a product. Common products may have a higher number of adverse events due to the higher total number of people using the product. openFDA, FDA

FDA adds: "Although MDRs are a valuable source of information, this passive surveillance system has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data. In addition, the incidence or prevalence of an event cannot be determined from this reporting system alone due to potential under-reporting of events and lack of information about frequency of device use." And: "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices."

Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated.

Not medical advice. This site counts what was reported to FDA. Questions about a medicine or device belong with a pharmacist or clinician.

2,351
reports naming it as manufacturer: 0% of all MAUDE reports; 0
reports, 12 months to August 2026: 0 in the 12 months before; 2%
classified as malfunction: 62.3% across all reports; 7.3%
classified as death, as reported: 0.9% across all reports

2,351 medical device reports received by FDA give St Jude Medical Puerto Rico as the manufacturer of the device involved, 0% of the MAUDE database, from January 1997 to November 2022. Manufacturer names are as written on the report; subsidiaries and spelling variants may appear as separate names.

0 reports arrived in the 12 months to August 2026, and none in the 12 months before. FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases. The event types recorded are injury (89%), death (7.3%) and malfunction (2%). Manufacturers are required to report events they learn of, so a large manufacturer with many products in use files many reports. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."

Brands named most often

Brand	Device type	Reports	Latest 12 months	Classified as death
6f Angio-Seal Vascular Closure Device Vip	Device, hemostasis, vascular	452	0	4%
Sjm Masters Series Mechanical Heart Valve	Heart-valve, mechanical	157	0	12.4%
Angio-Seal Vip Vascular Closure Device	Device, hemostasis, vascular	150	0	3.4%
Sjm Regent Heart Valve W/Flex Cuff	Heart-valve, mechanical	140	0	13%
6f Angio-Seal Vascular Closure Device Sts Plus	Device, hemostasis, vascular	127	0	2.8%
Sjm Mechanical Heart Valve	Heart-valve, mechanical	105	0	7.9%
Standard Cuff	Heart-valve, mechanical	87	0	10.6%
6f Angio-Seal Vascular Closure Device Sts	Device, hemostasis, vascular	71	0	5.1%
6f Angio-Seal Vascular Closure Device	Device, hemostasis, vascular	44	0	6.9%
Angio-Seal Device	Device, hemostasis, vascular	20	0	3.2%
8f Angio-Seal Vascular Closure Device Sts Plus	Device, hemostasis, vascular	4	0	4.7%
6f Angio-Seal Evolution	Device, hemostasis, vascular	3	0	3.9%
Durata Sts Optim Active Fixation Df-4 Connector	Permanent defibrillator electrodes	1	1,784	3.9%
Quadra Allure MP CRT-P	Pulse generator, pacemaker, implantable, with cardiac resynchronization (crt-p)	1	205	2.2%
Sjm Trifecta Valve	Heart-valve, non-allograft tissue	1	0	8.1%
Trifecta Stented Tissue Valve	Heart-valve, non-allograft tissue	1	0	7.9%

Brands with a page on this site, ordered by report count for navigation only. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."

Device types

Product code	Device type	Reports	Share
LWQ	Heart-valve, mechanical	1,165	49.6%
MGB	Device, hemostasis, vascular	1,111	47.3%
KRH	Ring, annuloplasty	49	2.1%
DXC	Clamp, vascular	12	0.5%
LWR	Heart-valve, non-allograft tissue	5	0.2%
NVZ	Pulse generator, permanent, implantable	3	0.1%
NVN	Drug eluting permanent right ventricular (rv) or right atrial (ra) pacemaker electrodes	2	0.1%
DXY	Implantable pacemaker pulse-generator	1	0%
LWS	Implantable cardioverter defibrillator (non-crt)	1	0%
MAF	Stent, coronary	1	0%

Reports by month, five years

FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases.

Event type

Death7.3%172

Injury89%2,092

Malfunction2%48

Other1.2%29

Not given0.4%10

Grey bar: all 26,136,888 MAUDE reports. Event type is the filer's classification and is not verified by FDA.

Questions about St Jude Medical Puerto Rico reports

How many FDA device reports name St Jude Medical Puerto Rico as manufacturer?

2,351 reports through August 2026, 0 of them in the latest 12 months.

Which of its brands appear most often?

6f Angio-Seal Vascular Closure Device Vip (452), Sjm Masters Series Mechanical Heart Valve (157), Angio-Seal Vip Vascular Closure Device (150), Sjm Regent Heart Valve W/Flex Cuff (140) and 6f Angio-Seal Vascular Closure Device Sts Plus (127).

Which device types does it report on?

heart-valve, mechanical (49.6%), device, hemostasis, vascular (47.3%), ring, annuloplasty (2.1%) and clamp, vascular (0.5%).

Does a high count say something about the manufacturer?

Not by itself. Manufacturers must file a report for every event they become aware of, so report volume follows the number of devices in use. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."

Where this comes from. Counts are built from the openFDA Device Adverse Event (MAUDE) bulk export released 28 Sep 2026, which holds reports FDA received through 31 Aug 2026. Brand, generic and manufacturer names are as written on the reports; product code names come from FDA's device classification. Manufacturer names are pooled after company suffixes (Inc., LLC, GmbH and similar) are dropped; names that read as a person rather than an organisation are never published. No report narrative, lot number, patient detail or reporter identity is published. See the methodology and sources; FDA's record is authoritative, and corrections are handled within five working days.

Drug data (FAERS) through 30 Jun 2026; device data (MAUDE) through 31 Aug 2026. Not medical advice.