ARROW INTERNATIONAL, LLC: 39 recalls on record

Recalls filed with 1 agency: FDA (39).

First recall on record: May 20, 2026. Most recent: June 24, 2026.

Risk classification: Class I: 39

Most recent recalls

DateAgencyProduct
June 24, 2026FDADescription/REF: PI AGBA PICC KIT: 3L 6 FR X 40 CM W/VPS/ASK-44063-NS AGBA PICC/DELTA: …Z-2370-2026
June 24, 2026FDADescription/REF: ACCESS TRAY/ASK-04001-MC3Z-2392-2026
June 24, 2026FDADescription/REF: AHDC KIT: 3-L 12 FR X 16 CM/AK-12123-PCDC; AHDC KIT: 3-L 12 FR X 20 CM…Z-2374-2026
June 24, 2026FDADescription/REF: HEMODIALYSIS KIT: 2-LUMEN 12 FR X 20 CM/AK-15122-F, AHDC KIT: 3L 12 FR X…Z-2388-2026
June 24, 2026FDADescription/REF: CVC/PSI KIT: 2 LUMEN 8 FR X 6 IN/ASK-42802-PLH; CVC KIT: 3-LUMEN 12 FR X…Z-2376-2026
June 24, 2026FDADescription/REF: HEMODIALYSIS KIT: 2L 14 FR X 20 CM AGB CDC-25142-X1AZ-2372-2026
June 24, 2026FDADescription/REF: BIOPSY SYSTEM COMPREHENSIVE KIT/ASK-09458-AH, ASK-09458-COC, ASK-09458-…Z-2365-2026
June 24, 2026FDADescription/REF: ACCESS TRAY/GU-04020; PSI KIT: 8.5 FR/AK-09803-CDC; PSI KIT: 9 FR/AK-099…Z-2385-2026
June 24, 2026FDADescription/REF: PI PICC: 3: 6FR x 55CM w CHG/ DLX-35563-HPKC; AGBA PICC: 2L 5.5 FR X 45 …Z-2378-2026
June 24, 2026FDADescription/REF: PICC ACCESS TRAY/ASK-04001-CG1Z-2395-2026
May 20, 2026FDAArrow-Clark VectorFlow Antegrade Chronic Hemodialysis Catheter: REF: ACS-15192-VFI, ACS-1…Z-2157-2026
May 20, 2026FDANextStep Antegrade Chronic Hemodialysis Catheter, REF: AC-15192-SFX, AC-15232-SFX, CS-151…Z-2159-2026
May 20, 2026FDAArrow Edge Hemodialysis Catheterization Product, REF: CS-15242-I, CS-15282-I, CS-15322-IZ-2156-2026
May 20, 2026FDACannon II Plus Hemodialysis Catheter, REF: CS-15242-VSP, CS-15282-VSP, CS-15322-VSP, CS-1…Z-2158-2026

Questions about this company

How many recalls does ARROW INTERNATIONAL, LLC have?
Recalert has 39 U.S. recalls on record for ARROW INTERNATIONAL, LLC, published between May 20, 2026 and June 24, 2026.
Which agencies have handled ARROW INTERNATIONAL, LLC recalls?
ARROW INTERNATIONAL, LLC appears as the recalling firm in recalls from: FDA (39).

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