Yahoo Finance

Teleflex catheterization kit recall linked to 10 injuries, 1 death

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Cardiovascular Business

Cath lab procedure kits recalled due to ongoing safety concern

The manifolds inside these kits have been linked to a significant risk of contamination. The FDA is urging users to place a warning label on each kit.
Medscape

Arrow QuickFlash Radial Artery Catheterization Kits Recalled

Teleflex and its subsidiary Arrow International have recalled the Arrow QuickFlash radial artery and radial artery/arterial line catheterization kits over a potentially defective component. The ...
Yahoo Finance

Catheter Kit Billing Fraud: "The Medicare Fraud of the Month for February"

ALBANY, N.Y. , Feb. 9, 2026 /PRNewswire/ -- The New York StateWide Senior Action Council (StateWide), a 54-year-old non-profit organization dedicated to serving the needs and well-being of our State's ...
TCTMD

Class I Recall for 330,000 Radial Artery Catheterization Kits: FDA

Device manufacturer Teleflex, and its subsidiary Arrow International, are recalling certain radial artery catheterization kits following reports of malfunction in both the guidewire handle and chamber ...
Healio

FDA designates recall of central venous access, catheter kits as class I

Please provide your email address to receive an email when new articles are posted on . The FDA announced that Teleflex and Arrow International LLC are recalling both the Arrow MAC Two-Lumen Central ...
Becker's Hospital Review

Catheterization kits recalled after 10 injuries, 1 death: FDA

Teleflex and its subsidiary Arrow International recalled 334,995 catheter kits after receiving reports of increased resistance in the guidewire handle and chamber during use, the FDA said April 3. The ...
Healio

Two intra-aortic balloon catheter kits recalled; three deaths reported

Please provide your email address to receive an email when new articles are posted on . The recall of two varieties of intra-aortic balloon catheter kits has been ...
BioWorld

FDA deems Teleflex/Arrow recall of catheter kits a class I event

The FDA posted a recall announcement for two catheter kits made by Arrow International LLC, a subsidiary of Wayne, Pa.-based Teleflex Inc., due to problems with the connectors used in the kits. While ...
MD&M East

Teleflex Arrow FiberOptix and UltraFlex (IAB) Catheter Kits Recall Identified as FDA Class I

Teleflex and its subsidiary Arrow International recently received FDA Class I designation for its recall of the Arrow FiberOptix and UltraFlex Intra-Aortic Balloon (IAB) catheter kits after reporting ...
Medscape

SHEA 2009: Inappropriate Catheterization Is Common

March 24, 2009 (San Diego, California) — Inappropriate urinary catheterization in hospitalized patients is common but should not be used as a remedy for incontinence because it is significantly ...