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HomeUROCARE PRODUCTS, INC. › Urocare® Universal Fabric Leg Bag Straps with Velcro® Closue (Set of 2)

Urocare® Universal Fabric Leg Bag Straps with Velcro® Closue (Set of 2)

UROCARE PRODUCTS, INC. · Model 6390 · UDI-DI 00792293063908

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10
510(k) clearances
2,118
Adverse events
21
Recalls
125
Facilities

Description

STRAP, LEG BAG, LATEX-FREE, VELCRO, UNIVERSAL, REUSABLE For use with most vinyl disposable or latex reusable leg bags. They are an economical alternative to the standard latex rubber straps packaged with most urine collection bags. An elastic/cotton & body construction allows the self-gripping fastener to attach itself along the length of the strap making it fully adjustable to individual requirements providing a safe, secure hold with a comfortable fit. A special blend of elastic and cotton makes them durable and allows them to be hand or machine washed. Set Contains: 2 Universal Leg straps and Illustrated Use and Care Instructions. * STRAPS NOT SOLD SEPARATELY ** BAGS MUST HAVE STRAP LOOPS/EYELETS FOR STRAPS TO PASS THROUGH

Recalls

DateFirmReason
2026-06-25C.R. Bard IncDue to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.
2026-06-25C.R. Bard IncDue to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.
2023-12-04Cardinal Health 200, LLCConvenience kits were manufactured and distributed with components which were subsequently recalled by Nurse Assist.
2019-01-14Teleflex MedicalThe device labels are not UDI compliant. The missing UDI compliance information on the labelling is not likely to affect the function/performance of the device itself. Other label
2019-01-14Teleflex MedicalThe device labels are not UDI compliant. The missing UDI compliance information on the labelling would not affect the function/performance of the device itself. Other label informa
2017-06-02C.R. Bard, Inc.Customer complaint of a cut in the side of the leg bag, indicating a potential breach of the product's sterile barrier.
2016-07-11C.R. Bard, Inc.The product contained a latex catheter instead of a silicone catheter.
2016-06-29C.R. Bard, Inc.Labeling problem
2015-07-10Customed, IncRecall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
2015-07-10Customed, IncRecall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.

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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.