PlainRecalls

Arrow International Inc

Compiled from official public sources by the editorial team.

478 recalls on record · Latest: Oct 2, 2024

Arrow International Inc Recall Insight

Arrow International Inc appears on 478 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.470% of the federal archive, a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Oct 2, 2024, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 50 entries, severity tagging shows 0 critical, 50 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 47 of 50 entries, unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (50). The date window on this page runs from Apr 18, 2018 to Jun 6, 2018.

Manufacturer-level browsing is useful when monitoring a single firm for patterns, whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current, deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement, always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

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 C…

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 …

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 P…

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 Pr…

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-…

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-…

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 Int…

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 Pre…

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…

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 Max…

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 Precauti…

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…

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; …

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; P…

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-…

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) Cat…

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+ …

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 T…

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Data Sources

  • Source: FDA + CPSC + NHTSA - federal recall filings naming this firm. Verify with FDA, CPSC, or NHTSA directly.
  • Source: PlainRecalls Manufacturer Index - firm-level aggregation across all three federal recall feeds

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.