The Recall Desk

Manufacturer

ARROW INTERNATIONAL Inc.

478 recalls in our database name ARROW INTERNATIONAL Inc. as the manufacturing or recalling firm.

What the numbers show

Total
478
Critical
1
Severe
136
Most recent
2024-10-02

Of the 478 recalls from ARROW INTERNATIONAL Inc. we have scored against our rubric, 1 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 136 (28%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

476–478 of 478

  • ModerateFDA (Devices)·Z-1057-2013·2013-04-10

    Arrow Berman Angiographic Catheter Recall Due to Outdated Contrast Medium Labeling

    Arrow International is recalling Berman Angiographic Catheters because the instructions reference a discontinued contrast medium. The firm is updating the labeling.

    Product
    Arrow/Teleflex Medical Berman Angiographic Balloon Catheter and Reverse Berman Angiographic Balloon Catheter. The Arrow Berman(TM) Angiographic Catheter is indicated for use in right heart catheterization for cardiac angiography, and measurement of the right heart and pulmonar
    Category
    Medical Device
    Distribution
    50 states
  • ModerateFDA (Devices)·Z-1830-2012·2012-07-04

    Arrow Central Venous Catheter Recall for Labeling Inconsistency

    Arrow International is recalling 634,912 central venous catheter sets because the product label states 'contains no medication' while the insert indicates the product is medicated.

    Product
    Arrow Two-Lumen Central Venous Catheterization Set with Blue FlexTip(R) ARROWgard Blue(R) Catheter Product Usage: The multiple-lumen catheter permits venous access to central circulation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1823-2012·2012-06-27

    Arrow Recalls Central Venous Catheters Due to Potential Hub Voids

    Arrow International is recalling 1,085 units of 7FR 3-Lumen Arrowg+ard Blue Plus Central Venous Catheters due to potential voids in the catheter hub that could cause interlumen crossover.

    Product
    Arrow International, Inc. 7FR 3-Lumen Arrowg+ard Blue Plus(R) Pressure Injectable Central Venous Catheter - Catalog number CDC-42703-XP1A The multiple-lumen pressure injectable catheter permits venous access to central circulation and injection of contrast media. The ARROWg+ar
    Category
    Medical Device
    Distribution
    Distributed nationwide