Device brand name · Proximate ils circular staplers
Proximate Proximate I L S Curved Intraluminal Staple: medical device reports filed with FDA
249 reports name it, 2002–2002. Manufacturer given most often on reports: Ethicon Endo-Surgery - Alb. Product code GAG.
- 249
- device reports naming the brand
- 0% of all MAUDE reports · about 10 a year
- 0
- reports, 12 months to August 2026
- 0 in the 12 months before
- 62.2%
- classified as malfunction
- 72.9% across the product code
- 1.2%
- classified as death, as reported
- 3 reports · not verified by FDA
249 medical device reports received by FDA name the brand "Proximate Proximate I L S Curved Intraluminal Staple" (proximate ils circular staplers); the manufacturer given most often on reports is Ethicon Endo-Surgery - Alb; received from February 2002 to October 2002. Brand names are as the reporter or manufacturer wrote them, so one product can appear under several spellings.
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 malfunction (62.2%), injury (33.3%) and death (1.2%); across all stapler, surgical reports (product code GAG) death is recorded in 1% and malfunction in 72.9%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are replace (61.4%), failure to form staple (38.6%) and failure to cut (23.7%). The patient problems coded most often are failure to anastomose, surgical procedure, additional and therapy/non-surgical treatment, additional. 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."
Reports by month, five years
No report naming Proximate Proximate I L S Curved Intraluminal Staple was received in the five years to August 2026; the latest was received in October 2002.
Event type and report source
Event type, as classified on the report
Who filed the report
Grey bar: all 26,848 reports carrying product code GAG. Event type is the filer's classification and is not verified by FDA.
Device problems coded
| Device problem (FDA code) | Reports | Share | Share across product code |
|---|---|---|---|
| Replace | 153 | 61.4% | 35.2% |
| Failure to form staple | 96 | 38.6% | 27.4% |
| Failure to cut | 59 | 23.7% | 3.6% |
| Misfire | 35 | 14.1% | 8.9% |
| Difficult to removethe device was hard to remove | 32 | 12.9% | 5.7% |
| Failure to fire | 28 | 11.2% | 8.9% |
| Leak/splashthe device leaked | 24 | 9.6% | 1.5% |
| Sticking | 11 | 4.4% | 10.9% |
| Other (for use when an appropriate device code cannot be identified) | 9 | 3.6% | 1.2% |
| Suture line separation | 9 | 3.6% | 0.6% |
| Component missing | 6 | 2.4% | 3% |
| Loose | 4 | 1.6% | 0.5% |
| Suture line disruption | 4 | 1.6% | 0.7% |
| Device issuea problem with the device | 3 | 1.2% | 15.9% |
| Difficult or delayed activation | 3 | 1.2% | 0% |
| Difficult or delayed positioning | 3 | 1.2% | 0% |
| Failure to deliverthe device did not deliver the dose or item | 3 | 1.2% | 0.8% |
| Detachment of device component | 2 | 0.8% | 1.8% |
FDA's device problem codes as entered on the report; one report can carry several. Generic codes such as "no apparent adverse event" are left out.
Patient problems coded
| Patient problem (FDA code) | Reports | Share |
|---|---|---|
| Failure to anastomose | 141 | 56.6% |
| Surgical procedure, additional | 63 | 25.3% |
| Therapy/non-surgical treatment, additional | 32 | 12.9% |
| Surgery, prolonged | 21 | 8.4% |
| Surgical procedure | 15 | 6% |
| Bleeding | 13 | 5.2% |
| Drainage | 8 | 3.2% |
| Colostomy | 7 | 2.8% |
| Surgical procedure, repeated | 6 | 2.4% |
| Fistula | 4 | 1.6% |
| Other (for use when an appropriate patient code cannot be identified) | 4 | 1.6% |
| Tissue damage | 4 | 1.6% |
| Deaththe patient died; cause not stated by this term | 3 | 1.2% |
| Fever | 3 | 1.2% |
| Post operative wound infection | 3 | 1.2% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Proximate Proximate I L S Curved Intraluminal Staple | Product code GAG | All MAUDE reports |
|---|---|---|---|
| Reports | 249 | 26,848 | 26,136,888 |
| Share of that pool | — | 0.9% | 0% |
| Classified as death, per 1,000 reports | 12 | 10 | 9 |
| Classified as injury | 33.3% | 25.1% | 36.2% |
| Classified as malfunction | 62.2% | 72.9% | 62.3% |
| Filed by the manufacturer | 100% | 91.8% | 94.9% |
Shares are of reports, not 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."
Other brands with product code GAG
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Endopath Endoscopic Multifeed Stapler | 1,706 | 0 | 0% |
| Proximate Linear Cutter | 1,776 | 1 | 1.3% |
| Eea | 4,922 | 542 | 0.8% |
| Gia | 4,899 | 404 | 0.9% |
| Proximate I L S Intraluminal Stapler | 709 | 0 | 2% |
| Proximate Reloadable Linear Stapler | 1,025 | 0 | 1.4% |
| Endo Gia Universal 12mm Single Use Inst | 1,077 | 0 | 1.8% |
| Auto Suture Roticulator 55-4 8 | 451 | 0 | 0.2% |
| Proximate Access 55 Articulating Linear Stapler | 398 | 0 | 0.5% |
| Ta | 1,541 | 142 | 1% |
| Auto Suture Premium Plus Ceea 31mm | 357 | 0 | 0.3% |
| Auto Suture Roticulator 55 Poly - 200 | 353 | 0 | 0% |
| Auto Suture Roticulator 55-3 5 | 314 | 0 | 0.6% |
| Endopath Endoscopic Linear Cutter | 322 | 0 | 0% |
| Echelon | 1,352 | 584 | 3.2% |
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." FDA also states that "common products may have a higher number of adverse events due to the higher total number of people using the product."
Questions about Proximate Proximate I L S Curved Intraluminal Staple reports
How many FDA reports name Proximate Proximate I L S Curved Intraluminal Staple?
249 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 0 in the latest 12 months.
What kinds of events are reported?
malfunction (62.2%), injury (33.3%) and death (1.2%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
replace (61.4%), failure to form staple (38.6%), failure to cut (23.7%), misfire (14.1%) and difficult to remove (12.9%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (100%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that Proximate Proximate I L S Curved Intraluminal Staple was at fault?
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." FDA adds that "a causal relationship cannot be established between product and reactions listed in a report."
How do I report a problem with a medical device?
Through FDA MedWatch (Form FDA 3500 for health professionals and consumers), or to the manufacturer. See the guide on how to report.
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. A report counts here when any device it lists carries this brand name after punctuation and capitalisation are normalised. 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.