Catheter for crossing total occlusions: medical device reports filed with FDA

1,386 reports carry this product code, 2013–2026; 6 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.

1,386
reports with this product code: 0% of all MAUDE reports; 192
reports, 12 months to August 2026: 151 in the 12 months before; 90.3%
classified as malfunction: 62.3% across all reports; 0.1%
classified as death, as reported: 0.9% across all reports

Product code PDU is FDA's classification for "Catheter for crossing total occlusions" (cardiovascular panel), a class 2 device. 1,386 medical device reports carry this product code, 0% of the MAUDE database, from November 2013 to August 2026.

192 reports arrived in the 12 months to August 2026, up 27% from 151 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 (90.3%), injury (9.5%) and death (0.1%). 6 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
Crosser	361	57	0%	97%
Crosser Cto Recanalization Catheter	256	0	0.3%	92%
Crosser Cto Recanalization Catheters	210	0	0%	93.7%
Crosser Recanalization Catheter	14	0	1.3%	81.8%
Outback Re-Entry Catheter	3	0	0%	84%
Bd	1	0	1%	56%

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
Bard Peripheral Vascular	1,033	74.5%
Cordis	80	5.8%
Volcano	49	3.5%
Cordis De Mexico	20	1.4%
Baylis Medical	12	0.9%
Cordis US	1	0.1%
Spectranetics	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

Death0.1%2

Injury9.5%131

Malfunction90.3%1,252

Other0%0

Not given0.1%1

Who filed

Manufacturer report97.9%1,357

Voluntary report1.3%18

User facility report0%0

Distributor report0%0

Not given0.8%11

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

Device problems coded

Device problem (FDA code)	Reports	Share
Material separation	651	47%
Detachment of device or device componentpart of the device came off	337	24.3%
Fracturea broken bone	137	9.9%
Device-device incompatibility	136	9.8%
Retraction problem	112	8.1%
Material deformation	91	6.6%
Breakthe device broke	89	6.4%
Failure to advance	66	4.8%
Material twisted/bent	64	4.6%
Material split, cut or torn	61	4.4%
Activation problem	45	3.2%
Difficult to removethe device was hard to remove	45	3.2%
Leak/splashthe device leaked	32	2.3%
Entrapment of device	25	1.8%
Torn material	25	1.8%
Material frayed	24	1.7%
Peeled/delaminated	24	1.7%
Device inoperablethe device could not be used	19	1.4%
Material puncture/hole	19	1.4%
Overheating of device	18	1.3%

Questions about catheter for crossing total occlusions reports

What is product code PDU?

FDA's classification code for "Catheter for crossing total occlusions", class 2, reviewed by the cardiovascular panel. Every device report carries the product code of the device involved.

How many reports carry this code?

1,386 reports through August 2026, 192 of them in the latest 12 months.

Which brands appear most often?

Crosser (361), Crosser Cto Recanalization Catheter (256), Crosser Cto Recanalization Catheters (210), Crosser Recanalization Catheter (14) and Outback Re-Entry Catheter (3). 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.