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SureCath Set
Coloplast A/S · Model 28028 · UDI-DI 05708932021111
EZD
Prescription
10
510(k) clearances
4,229
Adverse events (6 deaths)
13
Recalls
85
Facilities
Description
SureCath Set. Urinary catheter with attached bag for intermittent catheterization. Hydrophillic coated catheter. Nelaton. Male. FR 14/4.7 mm. Vol 1200 ml.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-04-20 | C.R. Bard Inc | Some catheters had a manufacturing defect where the clear resealing label separating from the product foil pouch, resulting in a possible opening into the product packaging that co |
| 2023-04-20 | C.R. Bard Inc | Some catheters had a manufacturing defect where the clear resealing label separating from the product foil pouch, resulting in a possible opening into the product packaging that co |
| 2023-04-20 | C.R. Bard Inc | Some catheters had a manufacturing defect where the clear resealing label separating from the product foil pouch, resulting in a possible opening into the product packaging that co |
| 2023-04-20 | C.R. Bard Inc | Some catheters had a manufacturing defect where the clear resealing label separating from the product foil pouch, resulting in a possible opening into the product packaging that co |
| 2020-06-17 | Wellspect HealthCare (Division of DENTSPLY IH AB) | Wellspect Healthcare is voluntarily recalling certain LoFric Origo" urethral catheters due to a potential defect which may be present in the catheter s distal tip. |
| 2020-06-17 | Wellspect HealthCare (Division of DENTSPLY IH AB) | Wellspect Healthcare is voluntarily recalling certain LoFric Origo" urethral catheters due to a potential defect which may be present in the catheters distal tip. |
| 2020-06-17 | Wellspect HealthCare (Division of DENTSPLY IH AB) | Wellspect Healthcare is voluntarily recalling certain LoFric Origo" urethral catheters due to a potential defect which may be present in the catheters distal tip. |
| 2017-09-14 | C.R. Bard, Inc. | Several instances of a catheter caught in the sterile barrier seal and in some instances cut catheters were observed. |
| 2017-09-14 | C.R. Bard, Inc. | Several instances of a catheter caught in the sterile barrier seal and in some instances cut catheters were observed. |
| 2017-09-14 | C.R. Bard, Inc. | Several instances of a catheter caught in the sterile barrier seal and in some instances cut catheters were observed. |
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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.