Transmitters and receivers, physiological signal, radiofrequency: medical device reports filed with FDA

1,726 reports carry this product code, 1996–2026; 8 brands with a page.

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.

1,726
reports with this product code: 0% of all MAUDE reports; 82
reports, 12 months to August 2026: 34 in the 12 months before; 91.5%
classified as malfunction: 62.3% across all reports; 4.2%
classified as death, as reported: 0.9% across all reports

Product code DRG is FDA's classification for "Transmitters and receivers, physiological signal, radiofrequency" (cardiovascular panel), a class 2 device. 1,726 medical device reports carry this product code, 0% of the MAUDE database, from May 1996 to August 2026.

82 reports arrived in the 12 months to August 2026, up 141% from 34 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 (91.5%), death (4.2%) and injury (3%). 8 brand names with a page on this site carry this code; the brands table is 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."

Brands with this product code

Brand	Reports	Latest 12 months	Classified as death	Classified as malfunction
Merlin@home, RF telemetry basic	697	45	0.1%	98.4%
Org-9110a	288	59	0%	100%
Zm-531pa	7	38	1.1%	96.7%
Philips	4	0	6.3%	78.9%
Datascope	1	0	7.3%	40.2%
Delta	1	22	7.2%	63.9%
PressureWire	1	80	1.8%	70.4%
Versacare	1	0	0.1%	97.6%

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."

Manufacturers named

Manufacturer (as written on reports)	Reports	Share
Nihon Kohden	497	28.8%
St Jude Medical Crm-Sylmar	376	21.8%
St Jude Medical	130	7.5%
Philips Medical Systems	23	1.3%
Covidien Mfg Dc Boulder	19	1.1%
Ge Healthcare	16	0.9%
Draeger Medical Systems	14	0.8%
St Jude Medical Crm-Kista	9	0.5%
Ge Medical Systems	2	0.1%
Mmj De Cv Usd	2	0.1%
Philips Healthcare	2	0.1%
Spacelabs Healthcare	2	0.1%
Agilent Technologies	1	0.1%
Datascope	1	0.1%
St Jude Medical - Neuromodulation	1	0.1%

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 and report source

Event type

Death4.2%73

Injury3%52

Malfunction91.5%1,579

Other0.6%11

Not given0.6%11

Who filed

Manufacturer report86.8%1,498

Voluntary report3.6%62

User facility report0%0

Distributor report4.3%74

Not given5.3%92

Grey bar: all 26,136,888 MAUDE reports.

Device problems coded

Device problem (FDA code)	Reports	Share
Communication or transmission problemthe device could not communicate or transmit	370	21.4%
Thermal decomposition of device	337	19.5%
Failure to power up	176	10.2%
Device operates differently than expectedthe device behaved unexpectedly	134	7.8%
Power conditioning problem	84	4.9%
Charred	82	4.8%
Device alarm system	62	3.6%
Overheating of device	58	3.4%
Device inoperablethe device could not be used	56	3.2%
Output problem	43	2.5%
Intermittent communication failure	37	2.1%
Computer software problema software problem	30	1.7%
No display/image	29	1.7%
Melted	25	1.4%
Device displays incorrect message	21	1.2%
Temperature problem	20	1.2%
Loss of powerthe device lost power	19	1.1%
Wireless communication problema wireless connection problem	19	1.1%
Breakthe device broke	17	1%
Unable to obtain readings	17	1%

Questions about transmitters and receivers, physiological signal, radiofrequency reports

What is product code DRG?

FDA's classification code for "Transmitters and receivers, physiological signal, radiofrequency", class 2, reviewed by the cardiovascular panel. Every device report carries the product code of the device involved.

How many reports carry this code?

1,726 reports through August 2026, 82 of them in the latest 12 months.

Which brands appear most often?

Merlin@home, RF telemetry basic (697), Org-9110a (288), Zm-531pa (7), Philips (4) and Datascope (1). Widely used products collect more reports because more people use them.

Can the brands table be used to rank the devices?

No. 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 differ in how many are in use, how long they have been sold and how reports are collected.

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. 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.