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Urocare® Fabric Foley® Catheter/Tubing Strap Large 22"

UROCARE PRODUCTS, INC. · Model 6312 · UDI-DI 00792293063120

KNXNNX
10
510(k) clearances
2,156
Adverse events
21
Recalls
125
Facilities

Description

STRAP, FABRIC, FOLEY, CATHETER, LATEX-FREE, VELCRO FASTENERS, REUSABLE There is an easier way to keep things in their place... Find out how easy it can be to attach your Foley® catheter or tubing with this elastic fabric strap. It's unique design distributes pressure evenly along the length of the strap offering a vast improvement in comfort while reducing the risk of bruising, pressure sores, pulled hair, circulation restriction and/or burns. The self-gripping fastener can engage anywhere along the length of the strap body making the strap fully adjustable to individual requirements. The durable material is hand or machine washable and the strap is available in multiple sizes Contains: 1 Fabric Catheter Strap, Use and Care Instructions

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 would not affect the function/performance of the device itself. Other label informa
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
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.