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
146
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 146 (31%) 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.

101–125 of 478

  • SevereFDA (Devices)·Z-1203-2020·2020-02-19

    Arrow International Recalls FlexTip Plus Epidural Catheterization Kits

    Arrow International is recalling FlexTip Plus Epidural Catheterization Kits because the included syringes may fail, potentially causing dural puncture.

    Product
    FlexTip Plus Epidural Catheterization Kit, Product Code JC-05400-E
    Category
    Medical Device
    Distribution
    37 states
  • SevereFDA (Devices)·Z-1206-2020·2020-02-19

    Arrow International Recalls FlexTip Plus Epidural Catheterization Sets

    Arrow International is recalling FlexTip Plus Epidural Catheterization Sets because the included syringes may fail, potentially causing dural puncture.

    Product
    FlexTip Plus Epidural Catheterization Set, Product Code MP-17019-TIP
    Category
    Medical Device
    Distribution
    37 states
  • SevereFDA (Devices)·Z-1180-2020·2020-02-19

    Arrow International Recalls FlexTip Plus Epidural Catheterization Kits

    Arrow International is recalling FlexTip Plus Epidural Catheterization Kits because the included syringes may fail, potentially causing dural puncture.

    Product
    FlexTip Plus Epidural Catheterization Kit, Product Code ASK-05501-SH
    Category
    Medical Device
    Distribution
    37 states
  • SevereFDA (Devices)·Z-1183-2020·2020-02-19

    Arrow International Recalls FlexTip Plus Combined Spinal Epidural Catheterization Kits

    Arrow International is recalling FlexTip Plus Combined Spinal Epidural Catheterization Kits because the included syringes may fail, potentially causing dural puncture.

    Product
    FlexTip Plus Combined Spinal Epidural Catheterization Kit, Product Code ASK-05560-TG1
    Category
    Medical Device
    Distribution
    37 states
  • SevereFDA (Devices)·Z-1212-2020·2020-02-19

    Arrow International Recalls FlexTip Plus Epidural Catheterization Kits

    Arrow International is recalling FlexTip Plus Epidural Catheterization Kits because the included syringes may fail, potentially causing dural puncture.

    Product
    FlexTip Plus Epidural Catheterization Kit, Product Code TI-05501-ME
    Category
    Medical Device
    Distribution
    37 states
  • SevereFDA (Devices)·Z-1179-2020·2020-02-19

    Arrow International Recalls FlexTip Plus Epidural Catheterization Kits

    Arrow International is recalling FlexTip Plus Epidural Catheterization Kits because the included syringes may fail, potentially causing dural puncture.

    Product
    FlexTip Plus Epidural Catheterization Kit, Product Code ASK-05400-CA1
    Category
    Medical Device
    Distribution
    37 states
  • SevereFDA (Devices)·Z-1172-2020·2020-02-19

    Arrow International Recalls FlexTip Plus Epidural Catheterization Kits

    Arrow International is recalling FlexTip Plus Epidural Catheterization Kits due to potential syringe failures that could cause dural puncture.

    Product
    FlexTip Plus Epidural Catheterization Kit, Product Code AK-05501
    Category
    Medical Device
    Distribution
    37 states
  • SevereFDA (Devices)·Z-1213-2020·2020-02-19

    Arrow International Recalls Epidural Catheterization Kits Due to Syringe Failure Risk

    Arrow International is recalling 343,105 Epidural Catheterization Kits with FlexTip Plus Catheters because the included loss of resistance syringes may fail, potentially causing dural puncture.

    Product
    Epidural Catheterization Kit with FlexTip Plus Catheter, Product Code TI-05520-EPI
    Category
    Medical Device
    Distribution
    37 states
  • SevereFDA (Devices)·Z-1176-2020·2020-02-19

    Arrow International Recalls FlexTip Plus Epidural Catheterization Kits

    Arrow International is recalling FlexTip Plus Epidural Catheterization Kits because the included syringes may fail, potentially causing dural puncture.

    Product
    FlexTip Plus Epidural Catheterization Kit, Product Code ASK-05500-TM
    Category
    Medical Device
    Distribution
    37 states
  • SevereFDA (Devices)·Z-1209-2020·2020-02-19

    Arrow International Recalls FlexTip Plus Epidural Catheterization Sets

    Arrow International is recalling FlexTip Plus Epidural Catheterization Sets because the included syringes may fail, potentially causing dural puncture.

    Product
    FlexTip Plus Epidural Catheterization Set, Product Code MTO-05500-TK
    Category
    Medical Device
    Distribution
    37 states
  • SevereFDA (Devices)·Z-1174-2020·2020-02-19

    Arrow International Recalls FlexTip Plus Epidural Catheterization Kits

    Arrow International is recalling FlexTip Plus Epidural Catheterization Kits because the included syringes may fail, potentially causing dural puncture.

    Product
    FlexTip Plus Epidural Catheterization Kit, Product Code ASK-02220-SRH
    Category
    Medical Device
    Distribution
    37 states
  • SevereFDA (Devices)·Z-1196-2020·2020-02-19

    Arrow International Recalls Pediatric Epidural Catheterization Sets Due to Syringe Failure Risk

    Arrow International is recalling FlexTip Plus Epidural Catheterization Sets for pediatric lumbar placement because the included loss of resistance syringes may fail, potentially causing dural puncture.

    Product
    FlexTip Plus Epidural Catheterization Set for Pediatric Lumbar Placement, Product Code EC-05520-P
    Category
    Medical Device
    Distribution
    37 states
  • SevereFDA (Devices)·Z-1205-2020·2020-02-19

    Arrow International Recalls 10 cc Luer-Slip Loss of Resistance Syringes

    Arrow International Inc is recalling 10 cc Luer-Slip Loss of Resistance Syringes due to potential failures that could result in dural puncture.

    Product
    10 cc Luer-Slip Loss of Resistance Syringe, Product Code LR-05501
    Category
    Medical Device
    Distribution
    37 states
  • SevereFDA (Devices)·Z-1181-2020·2020-02-19

    Arrow International Recalls Epidural Catheterization Kits Due to Syringe Failure Risk

    Arrow International is recalling specific lots of Epidural Catheterization Kits because the included syringes may fail, potentially causing dural puncture.

    Product
    Epidural Catheterization Kit with FlexTip Plus, Open Tip, Single- Port Catheter, Product Code ASK-05502-NY
    Category
    Medical Device
    Distribution
    37 states
  • SevereFDA (Devices)·Z-1170-2020·2020-02-19

    Arrow International Recalls FlexTip Plus Combined Spinal Epidural Catheterization Sets

    Arrow International Inc is recalling FlexTip Plus Combined Spinal Epidural Catheterization Sets because the included loss of resistance syringes may fail, potentially causing dural puncture.

    Product
    FlexTip Plus Combined Spinal Epidural Catheterization Set, Product Code AA-05400-B
    Category
    Medical Device
    Distribution
    37 states
  • SevereFDA (Devices)·Z-1185-2020·2020-02-19

    Arrow International Recalls FlexTip Plus Epidural Catheterization Kits

    Arrow International is recalling FlexTip Plus Epidural Catheterization Kits because the included syringes may fail, potentially causing dural puncture.

    Product
    FlexTip Plus Epidural Catheterization Kit, Product Code ASK-17019-MSC
    Category
    Medical Device
    Distribution
    37 states