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 50 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 Jun 26, 2019 to Feb 19, 2020.

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 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-…

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: …

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-ter…

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 …

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 ar…

FDA Devices Moderate Jun 26, 2019

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

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

Compare Arrow International Inc with Zimmer Biomet, Inc. →

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.