Devices › Ventilator, emergency, powered (resuscitator)
Device brand name · Ventilator emergency powered resuscitator
Pneupac: medical device reports filed with FDA
412 reports name it, 2017–2022. Manufacturer given most often on reports: Smiths Medical International. Product code BTL.
- 412
- device reports naming the brand
- 0% of all MAUDE reports · about 44 a year
- 0
- reports, 12 months to August 2026
- 0 in the 12 months before
- 97.1%
- classified as malfunction
- 95% across the product code
- 0%
- classified as death, as reported
- 0 reports · not verified by FDA
FDA's MAUDE database holds 412 reports that name the brand "Pneupac" (ventilator emergency powered resuscitator), received between February 2017 and December 2022; the manufacturer given most often on reports is Smiths Medical International. Spellings of one product vary from report to report.
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 (97.1%) and injury (2.9%); across all ventilator, emergency, powered (resuscitator) reports (product code BTL) death is recorded in 0.7% and malfunction in 95%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are device alarm system (19.7%), pressure problem (7.8%) and failure to cycle (6.8%). The patient problems coded most often are no patient involvement, apnea and low oxygen saturation. 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
Reports by the month FDA received them. FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases.
By year received
Event type and report source
Event type, as classified on the report
Who filed the report
Grey bar: all 4,753 reports carrying product code BTL. 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 |
|---|---|---|---|
| Device alarm system | 81 | 19.7% | 6.4% |
| Pressure problem | 32 | 7.8% | 16.3% |
| Failure to cycle | 28 | 6.8% | 5.3% |
| No audible alarm | 24 | 5.8% | 1.9% |
| Breakthe device broke | 19 | 4.6% | 18.9% |
| Gas/air leak | 17 | 4.1% | 3.6% |
| Mechanical problema mechanical problem | 17 | 4.1% | 3.1% |
| Power problem | 17 | 4.1% | 1% |
| Improper flow or infusion | 13 | 3.2% | 0.8% |
| Defective component | 12 | 2.9% | 2.8% |
| Leak/splashthe device leaked | 11 | 2.7% | 1.2% |
| Defective devicethe device was defective | 9 | 2.2% | 1.9% |
| Tidal volume fluctuations | 9 | 2.2% | 3.3% |
| Battery problema problem with the battery | 8 | 1.9% | 1.5% |
| Incorrect, inadequate or imprecise result or readings | 8 | 1.9% | 1.3% |
| Component missing | 7 | 1.7% | 1.9% |
| Device fell | 7 | 1.7% | 0.6% |
| Failure to power up | 7 | 1.7% | 0.8% |
| Infusion or flow problema problem with flow or infusion | 7 | 1.7% | 1% |
| Loose or intermittent connection | 7 | 1.7% | 2.4% |
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 |
|---|---|---|
| No patient involvement | 66 | 16% |
| Apnea | 5 | 1.2% |
| Low oxygen saturation | 4 | 1% |
| Hypoventilation | 2 | 0.5% |
| Respiratory insufficiency | 2 | 0.5% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Pneupac | Product code BTL | All MAUDE reports |
|---|---|---|---|
| Reports | 412 | 4,753 | 26,136,888 |
| Share of that pool | — | 8.7% | 0% |
| Classified as death, per 1,000 reports | 0 | 7 | 9 |
| Classified as injury | 2.9% | 3.5% | 36.2% |
| Classified as malfunction | 97.1% | 95% | 62.3% |
| Filed by the manufacturer | 99% | 97.3% | 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 BTL
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Neopuff Infant Resuscitator | 1,607 | 0 | 0% |
| Pneupac paraPAC plus | 700 | 37 | 0% |
| Pneupac Parapac Ventilator | 260 | 0 | 0.4% |
| Pneupac Ventilators Parapac Plus | 200 | 0 | 1% |
| Giraffe IRS | 165 | 54 | 0% |
| Puritan Bennett | 503 | 10 | 2.2% |
| Ventilator | 174 | 3 | 7.5% |
| Bear | 600 | 0 | 2.3% |
| Level One | 231 | 31 | 1.7% |
| Medfusion 3500 Pump | 636 | 15 | 0% |
| Octrode Lead Kit, 90cm Length | 3,742 | 329 | 0.2% |
| Portex Endotracheal Tubes | 223 | 36 | 0.4% |
| Portex General Anesthesia Circuits | 363 | 10 | 0% |
| Uni-Vent Model 731 | 3,305 | 0 | 0.3% |
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 Pneupac reports
How many FDA reports name Pneupac?
412 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 (97.1%) and injury (2.9%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
device alarm system (19.7%), pressure problem (7.8%), failure to cycle (6.8%), no audible alarm (5.8%) and break (4.6%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (99%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that Pneupac 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.