Device brand name · Disposable surgical stapler
Premium Plus Ceea 31 Instr W/Tilt-Top: medical device reports filed with FDA
441 reports name it, 2001–2017. Manufacturer given most often on reports: Ponce - Uss. Product code GAG.
- 441
- device reports naming the brand
- 0% of all MAUDE reports · about 18 a year
- 0
- reports, 12 months to August 2026
- 0 in the 12 months before
- 0.7%
- classified as malfunction
- 72.9% across the product code
- 1.1%
- classified as death, as reported
- 5 reports · not verified by FDA
441 medical device reports received by FDA name the brand "Premium Plus Ceea 31 Instr W/Tilt-Top" (disposable surgical stapler); the manufacturer given most often on reports is Ponce - Uss; received from September 2001 to March 2017. 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 injury (98%), death (1.1%) and malfunction (0.7%); 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 failure to cut (33.3%), difficult to remove (26.8%) and replace (25.6%). The patient problems coded most often are failure to anastomose, therapy/non-surgical treatment, additional and surgical procedure, 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 Premium Plus Ceea 31 Instr W/Tilt-Top was received in the five years to August 2026; the latest was received in March 2017.
By year received
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 |
|---|---|---|---|
| Failure to cut | 147 | 33.3% | 3.6% |
| Difficult to removethe device was hard to remove | 118 | 26.8% | 5.7% |
| Replace | 113 | 25.6% | 35.2% |
| Failure to form staple | 89 | 20.2% | 27.4% |
| Sticking | 50 | 11.3% | 10.9% |
| Leak/splashthe device leaked | 18 | 4.1% | 1.5% |
| Other (for use when an appropriate device code cannot be identified) | 16 | 3.6% | 1.2% |
| Device, removal of (non-implant) | 13 | 2.9% | 0.9% |
| Mechanical problema mechanical problem | 13 | 2.9% | 1.3% |
| Device operates differently than expectedthe device behaved unexpectedly | 11 | 2.5% | 0.3% |
| Detachment of device component | 10 | 2.3% | 1.8% |
| Entrapment of device | 9 | 2% | 0.4% |
| Misfire | 8 | 1.8% | 8.9% |
| Component missing | 6 | 1.4% | 3% |
| Insufficient device problem information | 6 | 1.4% | 0.3% |
| Breakthe device broke | 5 | 1.1% | 1.9% |
| Device issuea problem with the device | 5 | 1.1% | 15.9% |
| Device, or device fragments remain in patient | 4 | 0.9% | 0.2% |
| Difficult to open or close | 4 | 0.9% | 0.8% |
| Failure to fire | 4 | 0.9% | 8.9% |
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 | 120 | 27.2% |
| Therapy/non-surgical treatment, additional | 86 | 19.5% |
| Surgical procedure, additional | 72 | 16.3% |
| Tissue damage | 54 | 12.2% |
| Surgery, prolonged | 48 | 10.9% |
| Hemorrhage/blood loss/bleeding | 21 | 4.8% |
| Dural tear | 18 | 4.1% |
| Bleeding | 16 | 3.6% |
| Surgical incision, enlargement of | 15 | 3.4% |
| Colostomy | 13 | 2.9% |
| Foreign body, removal of | 12 | 2.7% |
| Anastomosis | 11 | 2.5% |
| Injurya physical injury | 10 | 2.3% |
| Hospitalization required | 9 | 2% |
| Surgical procedure, repeated | 9 | 2% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Premium Plus Ceea 31 Instr W/Tilt-Top | Product code GAG | All MAUDE reports |
|---|---|---|---|
| Reports | 441 | 26,848 | 26,136,888 |
| Share of that pool | — | 1.6% | 0% |
| Classified as death, per 1,000 reports | 11 | 10 | 9 |
| Classified as injury | 98% | 25.1% | 36.2% |
| Classified as malfunction | 0.7% | 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 Premium Plus Ceea 31 Instr W/Tilt-Top reports
How many FDA reports name Premium Plus Ceea 31 Instr W/Tilt-Top?
441 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?
injury (98%), death (1.1%) and malfunction (0.7%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
failure to cut (33.3%), difficult to remove (26.8%), replace (25.6%), failure to form staple (20.2%) and sticking (11.3%). 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 Premium Plus Ceea 31 Instr W/Tilt-Top 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.