Device, removal, pacemaker electrode, percutaneous: medical device reports filed with FDA

1,566 reports carry this product code, 1993–2026; 5 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.

1,566
reports with this product code: 0% of all MAUDE reports; 118
reports, 12 months to August 2026: 63 in the 12 months before; 7.3%
classified as malfunction: 62.3% across all reports; 32.6%
classified as death, as reported: 0.9% across all reports

Product code MFA is FDA's classification for "Device, removal, pacemaker electrode, percutaneous" (unknown panel), a class 3 device. 1,566 medical device reports carry this product code, 0% of the MAUDE database, from August 1993 to August 2026.

118 reports arrived in the 12 months to August 2026, up 87% from 63 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 (59.4%), death (32.6%) and malfunction (7.3%). 5 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
Spectranetics Glidelight Laser Sheath	451	0	33.2%	4.4%
GlideLight Laser Sheath	308	118	29.2%	13.3%
Spectranetics 16f Glidelight Laser Sheath	161	0	32.7%	6.2%
Spectranetics Lead Locking Device	5	0	6.5%	6%
Spectranetics Tightrail Rotating Dilator Sheath	2	0	21.1%	19.9%

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
Spectranetics	1,078	68.8%
The Spectranetics	376	24%
Biotronik	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

Death32.6%511

Injury59.4%930

Malfunction7.3%115

Other0.4%7

Not given0.2%3

Who filed

Manufacturer report97.8%1,532

Voluntary report0.6%10

User facility report0%0

Distributor report0%0

Not given1.5%24

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

Device problems coded

Device problem (FDA code)	Reports	Share
Insufficient device problem information	318	20.3%
Device operates differently than expectedthe device behaved unexpectedly	58	3.7%
Breakthe device broke	57	3.6%
Difficult to removethe device was hard to remove	55	3.5%
Failure to advance	46	2.9%
Material separation	41	2.6%
Physical resistance	36	2.3%
Difficult to advance	34	2.2%
Fracturea broken bone	29	1.9%
Device inoperablethe device could not be used	19	1.2%
Entrapment of device	18	1.1%
Sticking	18	1.1%
Positioning problem	13	0.8%
Improper or incorrect procedure or method	9	0.6%
Deformation due to compressive stress	8	0.5%
Kinkedthe tube or line kinked	8	0.5%
Replace	8	0.5%
Split	7	0.4%
Material split, cut or torn	6	0.4%
Contamination	5	0.3%

Questions about device, removal, pacemaker electrode, percutaneous reports

What is product code MFA?

FDA's classification code for "Device, removal, pacemaker electrode, percutaneous", class 3, reviewed by the unknown panel. Every device report carries the product code of the device involved.

How many reports carry this code?

1,566 reports through August 2026, 118 of them in the latest 12 months.

Which brands appear most often?

Spectranetics Glidelight Laser Sheath (451), GlideLight Laser Sheath (308), Spectranetics 16f Glidelight Laser Sheath (161), Spectranetics Lead Locking Device (5) and Spectranetics Tightrail Rotating Dilator Sheath (2). 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.