Arrow International Inc: 158 recalls on record

Recalls filed with 1 agency: FDA (158).

First recall on record: June 27, 2012. Most recent: October 2, 2024.

Risk classification: Class I: 14 · Class II: 143 · Class III: 1

Most recent recalls

DateAgencyProduct
December 25, 2013FDAContinuous Peripheral Nerve Block Catheter Kit and Set Continuous Peripheral Nerve Blo…Z-0546-2014
December 18, 2013FDAArrow Transradial Artery Access products Arrow Transradial Artery Access products are …Z-0468-2014
August 21, 2013FDAArrow International, Inc. Two-Lumen CVC Kit with Blue Flex Tip Catheter. The multiple lum…Z-1965-2013
April 17, 2013FDAArrow International FiberOptix Intra-Aortic Balloon Catheter Kit (IAB) 8 Fr 30 cc; Prod…Z-1064-2013
April 17, 2013FDAArrow International FiberOptix Intra-Aortic Balloon Catheter Kit (IAB) 8 Fr 40 cc; Produ…Z-1065-2013
April 10, 2013FDAArrow/Teleflex Medical Berman Angiographic Balloon Catheter and Reverse Berman Angiograph…Z-1057-2013
July 4, 2012FDAArrow Two-Lumen Central Venous Catheterization Set with Blue FlexTip(R) ARROWgard Blue(R)…Z-1830-2012
June 27, 2012FDAArrow International, Inc. 7FR 3-Lumen Arrowg+ard Blue Plus(R) Pressure Injectable Central…Z-1823-2012

Questions about this company

How many recalls does Arrow International Inc have?
Recalert has 158 U.S. recalls on record for Arrow International Inc, published between June 27, 2012 and October 2, 2024.
Which agencies have handled Arrow International Inc recalls?
Arrow International Inc appears as the recalling firm in recalls from: FDA (158).

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