Home › C. R. Bard, Inc. › Personal Catheter™ Intermittent Catheter
Personal Catheter™ Intermittent Catheter
C. R. Bard, Inc. · Model 63918 · UDI-DI 00801741069390
MJC
Prescription
1
510(k) clearances
16,326
Adverse events (1 deaths)
22
Recalls
9
Facilities
Description
Personal Catheter™ Intermittent Catheter Antibacterial Coated Silicone, Male
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-07-17 | C.R. Bard Inc | Foley catheter trays have incorrect inserts, user may think:1)Silicone, when it's natural rubber latex, or 2)Natural rubber latex with infection control coating, when it's silicone |
| 2025-07-17 | C.R. Bard Inc | Foley catheter trays have incorrect inserts, user may think:1)Silicone, when it's natural rubber latex, or 2)Natural rubber latex with infection control coating, when it's silicone |
| 2025-07-17 | C.R. Bard Inc | Foley catheter trays have incorrect inserts, user may think:1)Silicone, when it's natural rubber latex, or 2)Natural rubber latex with infection control coating, when it's silicone |
| 2024-05-09 | C.R. Bard Inc | Some of the devices may function incorrectly resulting in no temperature display or erratic temperatures being displayed on the temperature monitoring devices. |
| 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. |
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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.