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FOOTPRINT MEDICAL, INC. · Model S1UDK6.5 · UDI-DI 00858778006478

EZD Prescription
1
510(k) clearances
4,229
Adverse events (6 deaths)
13
Recalls
85
Facilities

Description

6.5Fr Silicone Urinary Drainage Kit with Catheter

Recalls

DateFirmReason
2023-04-20C.R. Bard IncSome 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
2023-04-20C.R. Bard IncSome 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
2023-04-20C.R. Bard IncSome 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
2023-04-20C.R. Bard IncSome 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
2020-06-17Wellspect 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.
2020-06-17Wellspect 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.
2020-06-17Wellspect 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.
2017-09-14C.R. Bard, Inc.Several instances of a catheter caught in the sterile barrier seal and in some instances cut catheters were observed.
2017-09-14C.R. Bard, Inc.Several instances of a catheter caught in the sterile barrier seal and in some instances cut catheters were observed.
2017-09-14C.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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Data 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.