Devices › Collector, urine, (and accessories) for indwelling catheter
Device brand name · Drain bag
Bard Urinary Drainage Bag: medical device reports filed with FDA
243 reports name it, 2017–2026. Manufacturer given most often on reports: C R Bard Covington -1018233. Product code KNX.
- 243
- device reports naming the brand
- 0% of all MAUDE reports · about 26 a year
- 33
- reports, 12 months to August 2026
- 36 in the 12 months before
- 90.9%
- classified as malfunction
- 89.7% across the product code
- 0%
- classified as death, as reported
- 0 reports · not verified by FDA
243 medical device reports received by FDA name the brand "Bard Urinary Drainage Bag" (drain bag); the manufacturer given most often on reports is C R Bard Covington -1018233; received from April 2017 to August 2026. Brand names are as the reporter or manufacturer wrote them, so one product can appear under several spellings.
33 reports arrived in the 12 months to August 2026, close to the 36 of 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 (90.9%) and injury (9.1%); across all collector, urine, (and accessories) for indwelling catheter reports (product code KNX) death is recorded in 0% and malfunction in 89.7%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are restricted flow rate (27.2%), deformation due to compressive stress (23.9%) and fluid/blood leak (13.6%). The patient problems coded most often are urinary tract infection, appropriate clinical signs, symptoms and conditions term/code not available and no patient involvement. 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 2,156 reports carrying product code KNX. 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 |
|---|---|---|---|
| Restricted flow rate | 66 | 27.2% | 29.3% |
| Deformation due to compressive stress | 58 | 23.9% | 11% |
| Fluid/blood leak | 33 | 13.6% | 8.3% |
| Material twisted/bent | 28 | 11.5% | 3.7% |
| Component misassembled | 14 | 5.8% | 3.8% |
| No flow | 13 | 5.3% | 7.3% |
| Kinkedthe tube or line kinked | 8 | 3.3% | 2% |
| Material deformation | 8 | 3.3% | 1.2% |
| Device contamination with chemical or other material | 7 | 2.9% | 2.5% |
| Complete blockage | 4 | 1.6% | 0.8% |
| Component missing | 4 | 1.6% | 4% |
| Device operates differently than expectedthe device behaved unexpectedly | 4 | 1.6% | 2.8% |
| Inaccurate flow rate | 4 | 1.6% | 0.8% |
| Infusion or flow problema problem with flow or infusion | 4 | 1.6% | 1.3% |
| Material fragmentation | 4 | 1.6% | 1.1% |
| Material split, cut or torn | 4 | 1.6% | 0.6% |
| Nonstandard device | 4 | 1.6% | 0.6% |
| Obstruction of flow | 4 | 1.6% | 2.8% |
| Partial blockage | 4 | 1.6% | 2.5% |
| Material puncture/hole | 3 | 1.2% | 0.2% |
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 |
|---|---|---|
| Urinary tract infectionbladder or urinary infection | 10 | 4.1% |
| Appropriate clinical signs, symptoms and conditions term/code not available | 7 | 2.9% |
| No patient involvement | 7 | 2.9% |
| Skin inflammation/ irritation | 2 | 0.8% |
| Urinary retentionbeing unable to empty the bladder | 2 | 0.8% |
| Abrasion | 1 | 0.4% |
| Bacterial infectiona bacterial infection | 1 | 0.4% |
| Discomfortdiscomfort | 1 | 0.4% |
| Fungal infectiona fungal infection | 1 | 0.4% |
| Painpain, site not specified | 1 | 0.4% |
| Pressure sore/ulcer | 1 | 0.4% |
| Thrombus | 1 | 0.4% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Bard Urinary Drainage Bag | Product code KNX | All MAUDE reports |
|---|---|---|---|
| Reports | 243 | 2,156 | 26,136,888 |
| Share of that pool | — | 11.3% | 0% |
| Classified as death, per 1,000 reports | 0 | 0 | 9 |
| Classified as injury | 9.1% | 9.7% | 36.2% |
| Classified as malfunction | 90.9% | 89.7% | 62.3% |
| Filed by the manufacturer | 99.6% | 94.5% | 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 KNX
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Bard Urine Meter with Bag | 324 | 73 | 0% |
| Urine Collection | 239 | 0 | 0% |
| Bard Urinary Drainage Bag with Anti-Reflux Chamber | 189 | 20 | 0% |
| EnCor Biopsy Probe | 5,264 | 15 | 0% |
| Dover | 171 | 32 | 0.6% |
| Rusch | 285 | 0 | 1.8% |
| Kendall | 213 | 23 | 2.3% |
| All-In-One Container | 260 | 0 | 0% |
| Bardex Lubri-Sil I.C. All-Silicone Foley Catheter | 3,131 | 620 | 0% |
| Latex Foley Catheter | 1,368 | 7 | 0% |
| Surestep | 5,323 | 0 | 0.1% |
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 Bard Urinary Drainage Bag reports
How many FDA reports name Bard Urinary Drainage Bag?
243 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 33 in the latest 12 months.
What kinds of events are reported?
malfunction (90.9%) and injury (9.1%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
restricted flow rate (27.2%), deformation due to compressive stress (23.9%), fluid/blood leak (13.6%), material twisted/bent (11.5%) and component misassembled (5.8%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (99.6%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that Bard Urinary Drainage Bag 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.