Device manufacturer, as written on reports

Medtronic Puerto Rico Operations Juncos: medical device reports filed with FDA

2,947 reports name it as the manufacturer of the device involved, 2007–2026.

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.

2,947
reports naming it as manufacturer: 0% of all MAUDE reports; 28
reports, 12 months to August 2026: 8 in the 12 months before; 51.9%
classified as malfunction: 62.3% across all reports; 1.7%
classified as death, as reported: 0.9% across all reports

2,947 medical device reports received by FDA give Medtronic Puerto Rico Operations Juncos as the manufacturer of the device involved, 0% of the MAUDE database, from February 2007 to July 2026. Manufacturer names are as written on the report; subsidiaries and spelling variants may appear as separate names.

28 reports arrived in the 12 months to August 2026, up 250% from 8 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 malfunction (51.9%), injury (46.1%) and death (1.7%). 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
Restore Ultra	Stimulator, spinal-cord, totally implanted for pain relief	329	39	0.1%
Paradigm Real-Time Insulin Infusion Pump	Pump, infusion, insulin, to be used with invasive glucose sensor	212	0	0.3%
Soletra	Stimulator, electrical, implanted, for parkinsonian tremor	150	12	4.2%
Restore Prime Advanced	Stimulator, spinal-cord, totally implanted for pain relief	136	0	0.4%
Paradigm Real-Time Revel Insulin Infusion Pump	Pump, infusion, insulin, to be used with invasive glucose sensor	125	0	0.6%
Restore Advanced Rechargeable	Stimulator, spinal-cord, totally implanted for pain relief	106	0	0.6%
Interstim	Stimulator, electrical, implantable, for incontinence	89	1,522	0.2%
Restore Rechargable Neurostimulator	Stimulator, spinal-cord, totally implanted for pain relief	83	0	0.6%
Synergy	Coronary drug-eluting stent	83	84	3.5%
Restore Rechargeable Neurostimulator	Stimulator, spinal-cord, totally implanted for pain relief	76	0	1.1%
Activa Pc	Stimulator, electrical, implanted, for parkinsonian tremor	64	0	1.2%
Itrel 3	Stimulator, spinal-cord, totally implanted for pain relief	49	10	1.4%
Kinetra	Stimulator, electrical, implanted, for parkinsonian tremor	49	1	2.1%
Enterra	Intestinal stimulator	35	0	0.8%
Paradigm Insulin Infusion Pump	Pump, infusion, insulin	29	0	0.4%
Reservoir 1 8ml	Pump, infusion	20	0	0.1%
Consulta Crt-D	Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (crt-d)	19	0	5.9%
Reservoir 3ml	Pump, infusion	16	0	0.8%
Enrhythm	Pulse generator, permanent, implantable	15	0	9.9%
Restore Prime	Stimulator, spinal-cord, totally implanted for pain relief	12	2	1.1%
Intellis	Stimulator, spinal-cord, totally implanted for pain relief	11	4,743	0%
Pump Mmt-722nas Prdgm Ins V2 2 Sk En	Pump, infusion, insulin	7	0	2.6%
Reservoir 1 8 Ml	Pump, infusion	7	0	0.9%
Adapta	Pulse generator, permanent, implantable	4	279	7.4%
Maximo Vr	Implantable cardioverter defibrillator (non-crt)	4	0	8.1%
Protecta Xt Crt-D	Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (crt-d)	4	3	4.5%
Pump Mmt-715nas Prdgm Ins V2 1 Sk En	Pump, infusion, insulin	4	0	5.1%
Pump Mmt-722nab Prdgm Ins V2 2 Bl En	Pump, infusion, insulin	4	0	2.1%
530g Insulin Pump	Automated insulin dosing , threshold suspend	3	0	0.8%
Medtronic IPG	Pulse generator, permanent, implantable	3	114	15.1%

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
LGW	Stimulator, spinal-cord, totally implanted for pain relief	940	31.9%
LKK	Pump, infusion, implanted, programmable	580	19.7%
EZW	Stimulator, electrical, implantable, for incontinence	426	14.5%
MHY	Stimulator, electrical, implanted, for parkinsonian tremor	299	10.1%
OYC	Pump, infusion, insulin, to be used with invasive glucose sensor	220	7.5%
MDS	Sensor, glucose, invasive	138	4.7%
LZG	Pump, infusion, insulin	75	2.5%
NVZ	Pulse generator, permanent, implantable	63	2.1%
LWS	Implantable cardioverter defibrillator (non-crt)	49	1.7%
NIK	Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (crt-d)	48	1.6%

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

Death1.7%49

Injury46.1%1,360

Malfunction51.9%1,530

Other0.1%4

Not given0.1%4

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

Questions about Medtronic Puerto Rico Operations Juncos reports

How many FDA device reports name Medtronic Puerto Rico Operations Juncos as manufacturer?

2,947 reports through August 2026, 28 of them in the latest 12 months.

Which of its brands appear most often?

Restore Ultra (329), Paradigm Real-Time Insulin Infusion Pump (212), Soletra (150), Restore Prime Advanced (136) and Paradigm Real-Time Revel Insulin Infusion Pump (125).

Which device types does it report on?

stimulator, spinal-cord, totally implanted for pain relief (31.9%), pump, infusion, implanted, programmable (19.7%), stimulator, electrical, implantable, for incontinence (14.5%) and stimulator, electrical, implanted, for parkinsonian tremor (10.1%).

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.