Arrow International Inc.
478 recalls on record · Latest: Oct 2, 2024
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Agency notice ledger
Federal filing book Arrow International Inc. HEAVY-BOOK · SINGLE-AGENCY
#13 of 14,151 · 478 notices · 0.458% archive
- BOOK 478 notices
- RANK #13 of 14,151
- SHARE 0.458% archive
- AGENCY FDA Devices (478)
- CAT medical devices
- CATS 1 category
- LATEST Oct 2, 2024
- PHOTO Ge Healthcare LLC
Nearest notice-volume peer: Ge Healthcare LLC (3 notice gap)
Arrow International Inc. accounts for about 0.458% of the 104,423-notice archive on 478 distinct filings — a heavy share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →
How Arrow International Inc. compares to 14,151 recalling firms
Arrow International Inc. ranks 13th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.
Arrow International Inc. vs all firms by recall-notice count
Where this firm's archive sits among every tracked recalling manufacturer
478 13th of 14151 higher than 14,138 of 14,151 firms
Firms, banded by distinct federal recall-event inventory
Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13
Arrow International Inc. in the notice-volume neighbourhood
Distinct federal recall events among this firm and nearest nationwide peers
- Medline Indus…
Medline Industries, LP
486 notices
- Arrow Interna… (this)
Arrow International Inc.
478 notices
- Ge Healthcare…
Ge Healthcare LLC
475 notices
- Attix Pharmac…
Attix Pharmaceuticals
470 notices
- King Bio Inc.
King Bio Inc.
465 notices
- Zimmer, Inc.
Zimmer, Inc.
446 notices
What this shows Arrow International Inc. holds about 0.458% of archive notices alongside 478 distinct filings.
FDA Devices Moderate Jun 6, 2018
Maximal Barrier Drape; Product Codes: ASK-00002-1A
FDA Devices Moderate Jun 6, 2018
Single-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Catheter and Sharps Safety Features; Product Codes: ASK-04301-TJ
FDA Devices Moderate Jun 6, 2018
5Fr. Catheter Clamp with Fastener; Product Code: CC-00005
FDA Devices Moderate Jun 6, 2018
ARROW JACC with Chlorag+ard Technology; Product Code: JR-42063-HPHNM and JR-42563-HPHNM
FDA Devices Moderate Jun 6, 2018
ARROWg+ard Blue(R) MAC(TM) Two-Lumen Central Venous Access Kit for use with 7-7.5 Fr. Catheters; Product Code: ASK-21142-WHC2
FDA Devices Moderate Jun 6, 2018
Percutaneous Sheath Introducer Kit with ARROWgard Blue¿ Sheath and Integral Hemostasis Valve/Side Port for use with 7 - 7.5 Fr. Catheters; Product Codes: MSO-29802-AHS and MSO-29903-AHS
FDA Devices Moderate Jun 6, 2018
MAC(TM) Two-Lumen Central Venous Access Kit with ARROWg+ard Blue(R) Access Device, Integral Hemostasis Valve and Sharps Safety Features for use with 7.5 - 8 Fr. Catheters; Product Code: ASK-21242-NYP and ASK-21242-PR
FDA Devices Moderate Jun 6, 2018
Percutaneous Sheath Introducer Kit with ARROWg+ard Blue(R) Sheath, Integral Hemostasis Valve/Side Port, Sharps Safety Features, and Maximal Barrier Precautions for use with 7.5 - 8 Fr. Catheters; Product Codes: ASK-29803-SJH, ASK-29903-SJH, and ASK-29903-UW1
FDA Devices Moderate Jun 6, 2018
Sheath Adapter with Cath-Gard¿ Catheter Contamination Shield for use with 4 - 7 Fr. Catheters; Product codes: SA-09847
FDA Devices Moderate Jun 6, 2018
Arterial Catheterization Kit; Product Codes: ASK-04020-DH
FDA Devices Moderate Jun 6, 2018
ARROWg+ard Blue PLUS¿ Pressure Injectable Two-Lumen CVC Kit; Product Code: CDC-42802-P1A
FDA Devices Moderate Jun 6, 2018
Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter, Sharps Safety Features, and Maximal Barrier Precautions; Product Codes: ASK-45703-SCH; ASK-45703-UAB, ASK-45703-VAH
FDA Devices Moderate Jun 6, 2018
Two-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Catheter and Sharps Safety Features; Product Code: ASK-15402-HOP
FDA Devices Moderate Jun 6, 2018
Echogenic Introducer Needle; Product Code: AN-04318
FDA Devices Moderate Jun 6, 2018
ARROWg+ard Blue¿ PSI Kit with Integral Hemostasis Valve/ Side Port for use with 7 - 7.5 Fr. Catheters; Product codes: SF-29803-1
FDA Devices Moderate Jun 6, 2018
Clear Fenestrated Drape with Adhesive; Product Code: CD-00001
FDA Devices Moderate Jun 6, 2018
Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter and Sharps Safety Features; Product Codes: ASK-42703-MHW and ASK-42703-OLL1
FDA Devices Moderate Jun 6, 2018
ARROW PICC Set; Product codes: PR-35563-HPHNL and PR-35563-HPHNM
FDA Devices Moderate Jun 6, 2018
Arrow PICC with Chlorag+ard Technology; Product codes: PR-44041-BAS, PR-44052-BAS, PR-44063-BAS, PR-45041-BAS, PR-45052-BAS, PR-45063-BAS, PR-45541-BAS,PR-45541-HPHNL, PR-45541-HPHNM, PR-45552-BAS, PR-45552-HPHNL,PR-45552-HPHNM, PR-45563-BAS, PR-45563-HPHNL, PR-45563-HPHNM
FDA Devices Moderate Jun 6, 2018
Catheter Hemostasis Valve For use with .038" (.096 cm) dia. and smaller guide wires; Product Code: AI-07000
FDA Devices Moderate Jun 6, 2018
ARROWgard Blue PLUS¿ Multi-Lumen CVC Kit with Blue FlexTip¿ Catheter; Product Code: MSO-45703-AHS
FDA Devices Moderate Jun 6, 2018
9 Fr. Radiopaque Polyurethane Sheath/Dilator with Integral Hemostasis Valve/Side Port for use with 7 - 8 Fr. Catheters and Arrow Percutaneous Introducer System; Product codes: SS-09903-S
FDA Devices Moderate Jun 6, 2018
0.2 Micron Flat Epidural Filter; Product Code: EF-05500
FDA Devices Moderate Jun 6, 2018
Arrow-Johans" ECG Adapter for Right Atrial Electrocadiography (RAECG); Product Code: EG-04900
FDA Devices Moderate Jun 6, 2018
Pressure Injectable Multi-Lumen Central Venous Catheterization Kit; Product Code: ASK-15703-PHMC
FDA Devices Moderate Jun 6, 2018
Maximal Barrier Drape; Product Codes: ASK-00376-SU
FDA Devices Moderate Jun 6, 2018
Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter, Sharps Safety Features and Maximal Barrier Precautions; Product Code: ASK-42703-RV1
FDA Devices Moderate Jun 6, 2018
Double-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter and Sharps Safety Features; Product Codes: ASK-42802-VC and ASK-47702-VC
FDA Devices Moderate Jun 6, 2018
Echogenic Needle; Product codes: PN-00215-E and PN-00217-E
FDA Devices Moderate Jun 6, 2018
Spring Wire Guide Introducer Needle; Product Codes: AN-04320 and AN-04418
FDA Devices Moderate Jun 6, 2018
VPS TipTracker Stylet Accessory; Product codes: RHY-177-TTSAP
FDA Devices Moderate Jun 6, 2018
ARROWg+ard Blue(R) Central Venous Catheterization Kit; Product Code: ASK-24306-WHC1 and ASK-24306-WHC2
FDA Devices Moderate Jun 6, 2018
Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip¿, ARROWg+ard Blue PLUS¿ Catheter, Sharps Safety Features and Maximal Barrier Precautions; Product Codes: ASK-45703-LDP1, ASK-45703-PBHS, ASK-45703-PHMC
FDA Devices Moderate Jun 6, 2018
Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Catheter, Sharps Safety Features and Maximal Barrier Precautions; Product Code: ASK-15703-LDP1
FDA Devices Moderate Jun 6, 2018
Continuous Nerve Block Needle; Product Codes: AB-00090, AB-00150, AB-17040-N, AB-17080-N, AB-17110-N, AB-17140-N, AB-18080-N, AB-18110-N
FDA Devices Moderate Jun 6, 2018
Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter, Sharps Safety Features and Maximal Barrier Precautions; Product Code: ASK-42703-PHCH
FDA Devices Moderate Jun 6, 2018
ARROWg+ard Blue PLUS(R) Multi-Lumen Central Venous Catheterization Kit; Product Code: ASK-42703-SJH
FDA Devices Moderate Jun 6, 2018
SnapLock" Catheter/Syringe Adapter; Product Code: AS-05500
FDA Devices Moderate Jun 6, 2018
10 cc Luer-Slip Loss of Resistance Syringe; Product Code: LR-05501
FDA Devices Moderate Jun 6, 2018
Pressure Injectable Quad-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter and Sharps Safety Features; Product Codes: ASK-45854-PSFM and ASK-42854-PRR
FDA Devices Moderate Jun 6, 2018
Arterial Line Kit with Sharps Safety Features and Maximal Barrier Precautions; Product Code: ASK-04018-OH1
FDA Devices Moderate Jun 6, 2018
Pressure Injectable Two-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter and Sharps Safety Features; Product Code: ASK-45802-PHMW
FDA Devices Moderate Jun 6, 2018
Maximal Barrier Drape; Product Code: ASK-01000-UPMS
FDA Devices Moderate Jun 6, 2018
Pressure Injectable Multi-Lumen Central Venous Catheterization Kit; Product Code: ASK-15703-PVH and ASK-15703-PNYP
FDA Devices Moderate Jun 6, 2018
Spring-Wire Guide Introducer Catheter Assembly; Product Code: CN-04018
FDA Devices Moderate Jun 6, 2018
Radial Artery Catheterization Kit with Sharps Safety Features; Product Codes: ASK-04020-RIHM
FDA Devices Moderate Jun 6, 2018
Single-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) ARROWg+ard Blue(R) Catheter and Sharps Safety Features; Product Code: ASK-24306-VC
FDA Devices Moderate Apr 18, 2018
(1) Central Venous Catheterization Kit, Part Number (PN): ASK-04300-PHP; (2) Single-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Catheter, PN: ASK-04301-WBH; (3) Vessel Catheterization Kit, PN: ASK-04550-NYP
FDA Devices Moderate Apr 18, 2018
AGB+ Multi Lumen CVC Kit (1) Part Number (PN): CDC-42703-B1A, (2) PN: CDC-42802-1A, (3) CDC-45703-1A, (4) CDC-45703-A1A, (5) PN: CDC-45703-B1A; AGB+ Quad-Lumen CVC Kit (6) PN: CDC-42854-1A, (7) PN: CDC-45854-1A; AGB+ Two-Lumen CVC Kit (8) PN: CDC-45802-1A, (9) PN: CDC-45802-B1A, (10) PN: CDC-46702-1A, (11) CDC-47702-1A; (12) Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Catheter and Sharps Safety Features, PN: ASK-45703-AH
FDA Devices Moderate Apr 18, 2018
(1) Access Tray, Part Number (PN): ASK-04001-MS; Arrow Multi-Lumen CVC Kit (2) PN: CDC-12703-1A; (3) PN: CDC-15703-1A; (4) PN: CDC-15703-B1A; Arrow Two-Lumen CVC Kit (5) PN: CDC-12802-1A; (6) PN: CDC-15802-1A; (7) PN: CDC-17702-1A
Arrow International Inc. carries an outsized archive share
Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.
Similar recall count
Nearest multi-notice firms by distinct-event totals (478 here — heavy-book).
Similar medical devices volume
Nearest multi-notice firms in the same narrow category lane.
Frequently Asked Questions
How many federal recall notices name Arrow International Inc.? ▼
PlainRecalls indexes 478 distinct federal recall events naming Arrow International Inc., aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Arrow International Inc. sit among other recalling firms? ▼
Arrow International Inc. ranks #13 of 14,151 by distinct recall-event count among 14,151 firms in this archive (99th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Arrow International Inc.'s notices? ▼
FDA Devices accounts for 478 of this firm's 478 indexed notices.
What product category dominates Arrow International Inc.'s filing book? ▼
Filings for Arrow International Inc. span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Arrow International Inc.: 478 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.
Firm-level totals aggregate distinct federal recall events naming Arrow International Inc.; individual notices remain authoritative on each linked recall page.
Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026