Home › C. R. Bard, Inc. › Bard® Foley Tray With Bardex® Lubricath® Foley Catheter
Bard® Foley Tray With Bardex® Lubricath® Foley Catheter
C. R. Bard, Inc. · Model 947618 · UDI-DI 00801741024795
EZC
Prescription
7
510(k) clearances
10,370
Adverse events (1 deaths)
10
Recalls
26
Facilities
Description
Bard® Foley Tray With Bardex® Lubricath® Foley Catheter
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-06-03 | C.R. Bard Inc | Cather packaging may contain the incorrect French size. |
| 2021-08-05 | C.R. Bard Inc | There is potential for packaging defects that may impact the sterile barrier. |
| 2021-08-05 | C.R. Bard Inc | There is potential for packaging defects that may impact the sterile barrier. |
| 2021-08-05 | C.R. Bard Inc | There is potential for packaging defects that may impact the sterile barrier. |
| 2021-08-05 | C.R. Bard Inc | There is potential for packaging defects that may impact the sterile barrier. |
| 2021-08-05 | C.R. Bard Inc | There is potential for packaging defects that may impact the sterile barrier. |
| 2021-08-05 | C.R. Bard Inc | There is potential for packaging defects that may impact the sterile barrier. |
| 2021-08-05 | C.R. Bard Inc | There is potential for packaging defects that may impact the sterile barrier. |
| 2017-12-13 | C.R. Bard, Inc. | Foley Catheter with Incorrect Retainer Cap Print |
| 2012-06-29 | C.R. Bard, Inc., Urological Division | Incomplete seal on sterile packages of product. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.