Arrow International Inc
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.
EPIDURAL CATHETERIZATION KIT, Product Code DE-05400D-BO
FlexTip Plus Epidural Catheterization Set, Product Code MP-17019-TIP
EPIDURAL CATHETERIZATION KIT, Product Code UR-05501-EXP
10 cc Luer-Slip Loss of Resistance Syringe, Product Code LR-05501
EPIDURAL CATHETERIZATION KIT, Product Code ALZANO-05400-B
FlexTip Plus Epidural Catheterization Kit, Product Code ASK-02220-SRH
FlexTip Plus Epidural Catheterization Kit, Product Code ASK-05500-TM
EPIDURAL CATHETERIZATION KIT, Product Code BE-05400B-ETTEL
EPIDURAL CATHETERIZATION KIT, Product Code UR-05501
FlexTip Plus Epidural Catheterization Kit, Product Code CA-02220
EPIDURAL CATHETERIZATION KIT, Product Code FR-05501-12
EPIDURAL CATHETERIZATION KIT, Product Code AT-05501-LEO
FlexTip Plus Epidural Catheterization Kit, Product Code ASK-17019-MSC
EPIDURAL CATHETERIZATION KIT, Product Code BE-080180-CHH
EPIDURAL CATHETERIZATION KIT, Product Code UR-05501-FR1
EPIDURAL CATHETERIZATION KIT, Product Code BJC-05400-BEN
EPIDURAL CATHETERIZATION KIT, Product Code MTO-05500-SU
FlexTip Plus Epidural Catheterization Kit, Product Code AK-05500
EPIDURAL CATHETERIZATION KIT, Product Code FR-05501-10
FlexTip Plus Epidural Catheterization Set, Product Code MTO-05500-TK
FlexTip Plus Combined Spinal Epidural Catheterization Kit, Product Code ASK-05560-WH
EPIDURAL CATHETERIZATION KIT, Product Code AT-05501-LIN
Epidural Catheterization Kit with FlexTip Plus Catheter, Product Code TI-05520-EPI
FlexTip Plus Epidural Catheterization Kit, Product Code ASK-05501-SH
FlexTip Plus Combined Spinal Epidural Catheterization Kit, Product Code ASK-05560-TG1
EPIDURAL CATHETERIZATION KIT, Product Code BE-05400-DCSHO
FlexTip Plus Epidural Catheterization Kit, Product Code MP-17019-TKP
FlexTip Plus Combined Spinal Epidural Catheterization Set, Product Code AA-05400-B
EPIDURAL CATHETERIZATION KIT, Product Code BE-080180-BXL
EPIDURAL CATHETERIZATION KIT, Product Code CZ-05400-EPI
FlexTip Plus Combined Spinal Epidural Catheterization Kit, Product Code NYU-05500-1
FlexTip Plus Epidural Catheterization Set, Product Code JC-05400-B
EPIDURAL CATHETERIZATION KIT, Product Code BE-05400-DCHH
FlexTip Plus Combined Spinal Epidural Catheterization Kit, Product Code ASK-05500-BID
FlexTip Plus Epidural Catheterization Kit, Product Code JC-05400-E
EPIDURAL CATHETERIZATION KIT, Product Code FR-05501-04
FlexTip Plus Epidural Catheterization Kit, Product Code AK-05501
FlexTip Plus Epidural Catheterization Kit, Product Code ASK-05503-BID
EPIDURAL CATHETERIZATION KIT, Product Code MTO-09903-KU
FlexTip Plus Epidural Catheterization Kit, Product Code YC-02220
FlexTip Plus Epidural Catheterization Kit, Product Code TI-05501-ME
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-…
Arrow Endurance" Extended Dwell Peripheral Catheter System, REF: ASK-00820-FLH
Arrow Berman Angiographic Catheter 60cm Item Number: AI-07130-J
Arrow Berman Angiographic Catheter 50cc Item Number: AI-07130
Arrow AGB+ Multi-Lumen CVC Kit-catheter permits venous access to central circulation by way of subclavian, jugular, and femoral veins Product Code: …
Pediatric Two-Lumen Central Venous Catheterization Kit with Blue FlexTip ARROWg+ard Blue Catheter, REF AK-25502 Product Usage; Provide short-ter…
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 …
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…
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.
Data Sources
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.