PlainRecalls

Arrow International Inc.

Compiled from official public sources by the publisher.

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

notices

What this shows Arrow International Inc. holds about 0.458% of archive notices alongside 478 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Feb 19, 2020

EPIDURAL CATHETERIZATION KIT, Product Code DE-05400D-BO
FDA Devices Moderate Feb 19, 2020

FlexTip Plus Epidural Catheterization Set, Product Code MP-17019-TIP
FDA Devices Moderate Feb 19, 2020

EPIDURAL CATHETERIZATION KIT, Product Code UR-05501-EXP
FDA Devices Moderate Feb 19, 2020

10 cc Luer-Slip Loss of Resistance Syringe, Product Code LR-05501
FDA Devices Moderate Feb 19, 2020

EPIDURAL CATHETERIZATION KIT, Product Code ALZANO-05400-B
FDA Devices Moderate Feb 19, 2020

FlexTip Plus Epidural Catheterization Kit, Product Code ASK-02220-SRH
FDA Devices Moderate Feb 19, 2020

FlexTip Plus Epidural Catheterization Kit, Product Code ASK-05500-TM
FDA Devices Moderate Feb 19, 2020

EPIDURAL CATHETERIZATION KIT, Product Code BE-05400B-ETTEL
FDA Devices Moderate Feb 19, 2020

EPIDURAL CATHETERIZATION KIT, Product Code UR-05501
FDA Devices Moderate Feb 19, 2020

FlexTip Plus Epidural Catheterization Kit, Product Code CA-02220
FDA Devices Moderate Feb 19, 2020

EPIDURAL CATHETERIZATION KIT, Product Code FR-05501-12
FDA Devices Moderate Feb 19, 2020

EPIDURAL CATHETERIZATION KIT, Product Code AT-05501-LEO
FDA Devices Moderate Feb 19, 2020

FlexTip Plus Epidural Catheterization Kit, Product Code ASK-17019-MSC
FDA Devices Moderate Feb 19, 2020

EPIDURAL CATHETERIZATION KIT, Product Code BE-080180-CHH
FDA Devices Moderate Feb 19, 2020

EPIDURAL CATHETERIZATION KIT, Product Code UR-05501-FR1
FDA Devices Moderate Feb 19, 2020

EPIDURAL CATHETERIZATION KIT, Product Code BJC-05400-BEN
FDA Devices Moderate Feb 19, 2020

EPIDURAL CATHETERIZATION KIT, Product Code MTO-05500-SU
FDA Devices Moderate Feb 19, 2020

FlexTip Plus Epidural Catheterization Kit, Product Code AK-05500
FDA Devices Moderate Feb 19, 2020

EPIDURAL CATHETERIZATION KIT, Product Code FR-05501-10
FDA Devices Moderate Feb 19, 2020

FlexTip Plus Epidural Catheterization Set, Product Code MTO-05500-TK
FDA Devices Moderate Feb 19, 2020

FlexTip Plus Combined Spinal Epidural Catheterization Kit, Product Code ASK-05560-WH
FDA Devices Moderate Feb 19, 2020

EPIDURAL CATHETERIZATION KIT, Product Code AT-05501-LIN
FDA Devices Moderate Feb 19, 2020

Epidural Catheterization Kit with FlexTip Plus Catheter, Product Code TI-05520-EPI
FDA Devices Moderate Feb 19, 2020

FlexTip Plus Epidural Catheterization Kit, Product Code ASK-05501-SH
FDA Devices Moderate Feb 19, 2020

FlexTip Plus Combined Spinal Epidural Catheterization Kit, Product Code ASK-05560-TG1
FDA Devices Moderate Feb 19, 2020

EPIDURAL CATHETERIZATION KIT, Product Code BE-05400-DCSHO
FDA Devices Moderate Feb 19, 2020

FlexTip Plus Epidural Catheterization Kit, Product Code MP-17019-TKP
FDA Devices Moderate Feb 19, 2020

FlexTip Plus Combined Spinal Epidural Catheterization Set, Product Code AA-05400-B
FDA Devices Moderate Feb 19, 2020

EPIDURAL CATHETERIZATION KIT, Product Code BE-080180-BXL
FDA Devices Moderate Feb 19, 2020

EPIDURAL CATHETERIZATION KIT, Product Code CZ-05400-EPI
FDA Devices Moderate Feb 19, 2020

FlexTip Plus Combined Spinal Epidural Catheterization Kit, Product Code NYU-05500-1
FDA Devices Moderate Feb 19, 2020

FlexTip Plus Epidural Catheterization Set, Product Code JC-05400-B
FDA Devices Moderate Feb 19, 2020

EPIDURAL CATHETERIZATION KIT, Product Code BE-05400-DCHH
FDA Devices Moderate Feb 19, 2020

FlexTip Plus Combined Spinal Epidural Catheterization Kit, Product Code ASK-05500-BID
FDA Devices Moderate Feb 19, 2020

FlexTip Plus Epidural Catheterization Kit, Product Code JC-05400-E
FDA Devices Moderate Feb 19, 2020

EPIDURAL CATHETERIZATION KIT, Product Code FR-05501-04
FDA Devices Moderate Feb 19, 2020

FlexTip Plus Epidural Catheterization Kit, Product Code AK-05501
FDA Devices Moderate Feb 19, 2020

FlexTip Plus Epidural Catheterization Kit, Product Code ASK-05503-BID
FDA Devices Moderate Feb 19, 2020

EPIDURAL CATHETERIZATION KIT, Product Code MTO-09903-KU
FDA Devices Moderate Feb 19, 2020

FlexTip Plus Epidural Catheterization Kit, Product Code YC-02220
FDA Devices Moderate Feb 19, 2020

FlexTip Plus Epidural Catheterization Kit, Product Code TI-05501-ME
FDA Devices Moderate Jan 29, 2020

Arrow Arterial Catherization Kit-20 Ga. x 4.45 cm Radiopaque Polyurethane over 22 Ga. TW Introducer Needle with Integral .018" (0.46 mm) dia. Spring-Wire Guide Product Code: ASK-04020-PMC The Arrow¿ Arterial Catheterization device permits access to the peripheral arterial circulation or to other small vessels.
FDA Devices Moderate Jan 29, 2020

Arrow Endurance" Extended Dwell Peripheral Catheter System, REF: ASK-00820-FLH
FDA Devices Moderate Dec 25, 2019

Arrow Berman Angiographic Catheter 60cm Item Number: AI-07130-J
FDA Devices Moderate Dec 25, 2019

Arrow Berman Angiographic Catheter 50cc Item Number: AI-07130
FDA Devices Moderate Oct 30, 2019

Arrow AGB+ Multi-Lumen CVC Kit-catheter permits venous access to central circulation by way of subclavian, jugular, and femoral veins Product Code: CDC-42703-1A - Product Usage: The ARROWg+ard Blue PLUS catheter permits venous access to central circulation by way of subclavian, jugular, and femoral veins. The ARROWg+ard technology is intended to provide protection against catheter-related bloodstream infections (CRBSIs). It is not intended to be used as a treatment for existing infections nor i
FDA Devices Moderate Oct 16, 2019

Pediatric Two-Lumen Central Venous Catheterization Kit with Blue FlexTip ARROWg+ard Blue Catheter, REF AK-25502 Product Usage; Provide short-term (< 30 days) central venous access for treatment of diseases or conditions requiring central venous access
FDA Devices Moderate Oct 2, 2019

8.5 Fr. X 10 cm ARROW+gard Blue PSI Kit Cath-Gard for use with 7.5 - 8 Fr.Catheters Product Code: CDC-29803-1A - Product Usage: The MACTM Two-Lumen Central Venous Access Device with ARROWg+ard Blue¿ permits venous access and catheter introduction to the central circulation. It may be inserted into the jugular, subclavian, or femoral veins. The ARROWg+ard¿ technology is intended to help provide protection against catheter-related infections. Clinical data have not been collected that demonstrate
FDA Devices Moderate Oct 2, 2019

Arrow 8.5 Fr. X 16 cm Quad-Lumen Central Venous Catheterization Kit Product Code:AK-42854-P1A - Product Usage: The Arrow Central Venous Catheters are intended to permit venous access to the central circulation by way of the femoral, jugular or subclavian veins.
FDA Devices Moderate Jun 26, 2019

Arrow JACC with Chlorag+ard Technology Jugular Axillo subclavian Central Catheter Product Code: CDC 42552 JX1A

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).

Ge Healthcare LLC 475 Medline Industries, LP 486 Attix Pharmaceuticals 470 King Bio Inc. 465 Zimmer, Inc. 446

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

Ge Healthcare LLC 475 Medline Industries, LP 486 Zimmer, Inc. 446 Biomerieux Inc 422

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