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
March 6, 2019FDAAF w/AS 550 x 1-14ML/HR 5ML-60LO CPNB, Product code MVBX60XL CPNB, Arrow AutoFuser Dispos…Z-0956-2019
March 6, 2019FDAAF w/AS 550 x 1-14 ml/hr, 5ml30 LOCPNB, Product code MVBX30XLCPNB, Arrow AutoFuser Dispos…Z-0953-2019
July 18, 2018FDAVPS TipTracker Stylet Accessory, REF RHY-177-TTSAP Product Usage: To provide real tim…Z-2384-2018
July 18, 2018FDAPeripherally Inserted Midline Catheter Kit with Placement Wire, REF MK-02031-TW Produc…Z-2385-2018
June 6, 2018FDA4Fr. Catheter Clamp with Fastener; Product Code: CC-00004Z-2006-2018
June 6, 2018FDARadial Arterial Access Kit; Product Code: ASK-04001-BID2Z-1968-2018
June 6, 2018FDAPercutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port and Sharps Sa…Z-1977-2018
June 6, 2018FDAMaximal Barrier Drape; Product Code: ASK-04000-HMCZ-1967-2018
June 6, 2018FDA8Fr. Catheter Clamp with Fastener; Product Code: CC-00008Z-2009-2018
June 6, 2018FDAMulti-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS…Z-2003-2018
June 6, 2018FDAVPS Rhythm ECG Accessory Pack with Johans Adapter; Product codes: RHY-100-ECGJZ-2026-2018
June 6, 2018FDAPressure Injectable ARROWg+ard Blue PLUS(R) Multi-Lumen Central Venous Catheterization Ki…Z-1988-2018
June 6, 2018FDAEpidural Needle; Product Codes: AN-05501 and AN-05505Z-1961-2018
June 6, 2018FDAPeel Away Sheath over Dilator; Product Codes: PL-05041 and PL-05052Z-2021-2018
June 6, 2018FDAARROWg+ard Blue PLUS¿ Pressure Injectable Quad-Lumen CVC Kit; Product Codes: CDC-42854-P1…Z-1989-2018
June 6, 2018FDAArrow-Flex(R) Percutaneous Sheath Introducer Kit with ARROWg+ard Blue(R) Sheath and Integ…Z-1975-2018
June 6, 2018FDAPressure Injectable ARROWg+ard Blue PLUS(R) Two-Lumen Central Venous Catheterization Kit;…Z-1993-2018
April 18, 2018FDAAGB+ Multi Lumen CVC Kit (1) Part Number (PN): CDC-42703-B1A, (2) PN: CDC-42802-1A, (3) C…Z-1335-2018
April 18, 2018FDA(1) Central Venous Catheterization Kit, Part Number (PN): ASK-04300-PHP; (2) Single-Lumen…Z-1331-2018
April 11, 2018FDARadial Artery Catheterization Kit; Model: AK-04220Z-1286-2018
April 11, 2018FDARadial Artery Catheterization Kit; Model: AK-04020Z-1282-2018
March 28, 2018FDAARROWg+ard Blue PLUS Pressure Injectable Multi-Lumen CVC Kit. Intended to permit venou…Z-1166-2018
March 21, 2018FDAMulti-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Catheter and Sharps S…Z-0994-2018
March 21, 2018FDAARROWg+ard BLUE PLUS Pressure Injectable Two- Lumen CVC Kit Product Usage: The Arr…Z-1004-2018
February 28, 2018FDAARROWg+ard Blue Two Lumen Hemodialysis Catheterization Kit for High Volume Infusions; Pro…Z-0658-2018

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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