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
October 2, 2024FDAArrow Arterial Kits and Trays as follows: (1) Arrow Arterial Access Tray with 0.025" S…Z-3299-2024
June 12, 2024FDAArrow Ultra 8 IAB Intra-Aortic Balloon Catheter Kit, a) REF IAB-05830-U; b) REF IAB-058…Z-1880-2024
June 12, 2024FDAArrow UltraFlex Intra-Aortic Balloon Catheter Kit, a) REF IAB-06830-U; b) REF IAB-06840…Z-1879-2024
June 12, 2024FDAArrow FiberOptix Intra-Aortic Balloon Catheter Kit: a) REF IAB-05830-LWS; b) REF IAB-0…Z-1878-2024
March 27, 2024FDAARROW QuickFlash Radial Artery Catherization (wire, guide, catheter), Part Numbers: a)…Z-1267-2024
October 11, 2023FDAArrow ErgoPack Pressure Injectable Arrowg+ard Blue Advance Three-Lumen PICC pre-loaded wi…Z-0004-2024
September 27, 2023FDAArrow ErgoPack Pressure Injectable One-Lumen PICC, REF CDC-05541-HPK1A; catheter, intrava…Z-2590-2023
December 21, 2022FDAArrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-05001 (IP…Z-0455-2023
December 21, 2022FDAArrow AC3 Optimus Intra-Aortic Balloon Pump, AC3 Optimus IABP NA/EMEA, REF IAP-0700 (IPN…Z-0438-2023
December 21, 2022FDAArrow AutoCAT2 Intra-Aortic Balloon Pump, AEROAUTOCAT2 WAVE REFURBISHED, REF IAP-0535X (…Z-0432-2023
December 21, 2022FDAArrow AutoCAT2 Intra-Aortic Balloon Pump, AEROAUTOCAT 2 WAVE, REF IAP-0535 (IPN000329), …Z-0431-2023
October 26, 2022FDAARROW Pressure Injectable Arrowg+ard Blue Advance Two-Lumen Midline Kit, 5.5 Fr, 15 cm, .…Z-0102-2023
July 8, 2020FDAArrow AC3 Optimus Intra-Aortic Balloon Pump AC3 Optimus IABP NA/AJLA, Product Code IAP-07…Z-2417-2020
July 8, 2020FDAArrow AutoCAT2 Intra-Aortic Balloon Pump AUTOCAT2 WAVE, Product Code IAP-0500Z-2410-2020
July 8, 2020FDAArrow AutoCAT2 Intra-Aortic Balloon Pump AUTOCAT2 WAVE JAPANESE, Product Code IAP-0500JZ-2413-2020
July 8, 2020FDAArrow AutoCAT2 Intra-Aortic Balloon Pump AUTOCAT 2, Product Code IAP-0400Z-2408-2020
February 26, 2020FDAArrow Central Venous Catheterization Kit ASK-04200-UPMZ-1243-2020
February 26, 2020FDAArrow StimuCath(R) Continuous Nerve Block Kit ASK-05060-CHO1Z-1241-2020
February 26, 2020FDAArrow FlexTip Plus(R) Epidural Catheterization Kit ASK-05400-CA1Z-1236-2020
February 26, 2020FDAPICC Set- PR-35052-HPHNMZ-1254-2020
February 26, 2020FDAArrow FlexTip Plus(R) Combined Spinal Epidural Catheterization Kit ASK-05560-WHZ-1239-2020
February 19, 2020FDAEPIDURAL CATHETERIZATION KIT, Product Code IT-05400-DCZ-1200-2020
February 19, 2020FDAFlexTip Plus Epidural Catheterization Kit, Product Code ASK-05500-TMZ-1176-2020
February 19, 2020FDAEPIDURAL CATHETERIZATION KIT, Product Code JC-05400-LBZ-1204-2020
February 19, 2020FDAFlexTip Plus Epidural Catheterization Kit, Product Code ASK-02220-SRHZ-1174-2020

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.
What was the most recent Arrow International Inc recall?
FDA recall Z-3299-2024, published October 2, 2024: Arrow Arterial Kits and Trays as follows: (1) Arrow Arterial Access Tray with 0.025" Spring-Wire Guide (Catheter Not Included), REF ASK-04001-BW1; (2) Arrow Arterial Access Tray with 0.021" Sp…
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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