Manufacturer
478 recalls in our database name ARROW INTERNATIONAL Inc. as the manufacturing or recalling firm.
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.
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.
Arrow International Inc is recalling 140 units of Central Venous Catheterization Kits because the product lidstock contains the incorrect expiration date.
Arrow International Inc. is recalling 870 units of the Arrow Epidural Catheterization Kit because the product lidstock contains the incorrect expiration date.
Arrow International Inc. is recalling 205 units of the FlexTip Plus Epidural Catheterization Kit because the product lidstock contains the incorrect expiration date.
Arrow International Inc. is recalling 1,360 units of the Arrow Epidural Catheterization Kit CK-02220 because the product lidstock contains the incorrect expiration date.
Arrow International Inc. is recalling 160 units of the Arrow Epidural Catheterization Kit (YC-02220) because the product lidstock contains the incorrect expiration date.
Arrow International Inc. is recalling 1,320 units of the Arrow Epidural Catheterization Kit because the product lidstock contains the incorrect expiration date.
Arrow International Inc. is recalling 410 units of Arrow PSI Kits due to incorrect expiration dates on the product lidstock.
Arrow International Inc. is recalling 90 units of Arrow SPINAL ANESTHESIA SET ASA-25090-S because the product lidstock contains the incorrect expiration date.
Arrow International Inc is recalling PICC Sets (PR-35052-HPHNM) because the product lidstock contains the incorrect expiration date.
Arrow International Inc is recalling 1,760 units of the Arrow Epidural Catheterization Kit because the product lidstock contains the incorrect expiration date.
Arrow International Inc. is recalling 1,150 units of FlexTip Plus Combined Spinal Epidural Catheterization Kits because the product lidstock contains the incorrect expiration date.
Arrow International Inc. is recalling 180 units of the Arrow EPIDURAL NEEDLE KIT SL-05500 because the product lidstock contains the incorrect expiration date.
Arrow International is recalling specific lots of PICC kits because the lidstock displays the wrong expiration date.
Arrow International Inc is recalling 1,839 units of Arrow Epidural Needle Component AN-05505 because the product lidstock contains the incorrect expiration date.
Arrow International Inc is recalling Arrow FlexTip Plus Epidural Catheterization Kits because the product lidstock contains the incorrect expiration date.
Arrow International Inc is recalling 155 units of the StimuCath Continuous Nerve Block Kit because the product lidstock contains an incorrect expiration date.
Arrow International Inc is recalling 250 units of the Arrow FlexTip Plus Epidural Catheterization Kit because the product lidstock contains the incorrect expiration date.
Arrow International is recalling 343,105 Epidural Catheterization Kits because the included loss of resistance syringes may fail, potentially causing dural puncture.
Arrow International is recalling FlexTip Plus Epidural Catheterization Kits because the included syringes may fail, potentially causing dural puncture.
Arrow International is recalling 343,105 epidural catheterization kits because the included loss of resistance syringes may fail, potentially causing dural puncture.
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.
Arrow International Inc is recalling 343,105 Epidural Catheterization Kits because the included loss of resistance syringes may fail, potentially causing dural puncture.
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.
Arrow International is recalling FlexTip Plus Epidural Catheterization Kits because the included syringes may fail, potentially causing dural puncture.
Arrow International is recalling 343,105 Epidural Catheterization Kits because the included loss of resistance syringes may fail, potentially causing dural puncture.