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ARROW INTERNATIONAL Recalls
525 recalls on record · June 27, 2012 to June 24, 2026 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
February 26, 2020Medical DevicesFDA
Arrow International Inc recalls PICC Set- PR-35052-HPHNM
Hazard: Product lidstock contains the incorrect expiration date for the product
February 26, 2020Medical DevicesFDA
Arrow International Inc recalls (1) Arrow¿ STIM CPNB TUOHY NDL: 18G x 14CM (5-1/2") AB-18140-N (2) Arrow¿ STIM CPNB TUOHY NDL: 18G x 11CM (4-3/8") AB
Hazard: Product lidstock contains the incorrect expiration date for the product
February 26, 2020Medical DevicesFDA
Arrow International Inc recalls Arrow EPIDURAL NEEDLE KIT SL-05500
Hazard: Product lidstock contains the incorrect expiration date for the product
February 26, 2020Medical DevicesFDA
Arrow International Inc recalls Arrow EPIDURAL CATHETERIZATION COMPONENT EC-05000
Hazard: Product lidstock contains the incorrect expiration date for the product
February 26, 2020Medical DevicesFDA
Arrow International Inc recalls Arrow SPINAL ANESTHESIA SET ASA-25090-S
Hazard: Product lidstock contains the incorrect expiration date for the product
February 26, 2020Medical DevicesFDA
Arrow International Inc recalls Arrow EPIDURAL CATHETERIZATION KIT CK-02220
Hazard: Product lidstock contains the incorrect expiration date for the product
February 26, 2020Medical DevicesFDA
Arrow International Inc recalls Arrow EPIDURAL CATHETERIZATION KIT AM-05500
Hazard: Product lidstock contains the incorrect expiration date for the product
February 26, 2020Medical DevicesFDA
Arrow International Inc recalls Arrow EPIDURAL CATHETERIZATION KIT JH-05500
Hazard: Product lidstock contains the incorrect expiration date for the product
February 26, 2020Medical DevicesFDA
Arrow International Inc recalls Arrow EPIDURAL CATHETERIZATION KIT YC-02220
Hazard: Product lidstock contains the incorrect expiration date for the product
February 26, 2020Medical DevicesFDA
Arrow International Inc recalls Arrow¿ EPIDURAL CATHETERIZATION KIT AK-05000
Hazard: Product lidstock contains the incorrect expiration date for the product
February 26, 2020Medical DevicesFDA
Arrow International Inc recalls Arrow EPIDURAL NEEDLE COMPONENT AN-05505
Hazard: Product lidstock contains the incorrect expiration date for the product
February 26, 2020Medical DevicesFDA
Arrow International Inc recalls Arrow Central Venous Catheterization Kit ASK-04200-UPM
Hazard: Product lidstock contains the incorrect expiration date for the product
February 26, 2020Medical DevicesFDA
Arrow International Inc recalls Arrow PSI Kit for use with 7 - 7.5 Fr. Catheters ASK-09801-UPM
Hazard: Product lidstock contains the incorrect expiration date for the product
February 26, 2020Medical DevicesFDA
Arrow International Inc recalls Arrow StimuCath(R) Continuous Nerve Block Kit ASK-05060-CHO1
Hazard: Product lidstock contains the incorrect expiration date for the product
February 26, 2020Medical DevicesFDA
Arrow International Inc recalls Arrow Maximal Barrier Drape ASK-00002-1A
Hazard: Product lidstock contains the incorrect expiration date for the product
February 26, 2020Medical DevicesFDA
Arrow International Inc recalls Arrow FlexTip Plus(R) Combined Spinal Epidural Catheterization Kit ASK-05560-WH
Hazard: Product lidstock contains the incorrect expiration date for the product
February 26, 2020Medical DevicesFDA
Arrow International Inc recalls Arrow FlexTip Plus(R) Epidural Catheterization Kit ASK-05500-CAN
Hazard: Product lidstock contains the incorrect expiration date for the product
February 26, 2020Medical DevicesFDA
Arrow International Inc recalls Arrow FlexTip Plus(R) Epidural Catheterization Kit ASK-17019-MSC
Hazard: Product lidstock contains the incorrect expiration date for the product
February 26, 2020Medical DevicesFDA
Arrow International Inc recalls Arrow FlexTip Plus(R) Epidural Catheterization Kit ASK-05400-CA1
Hazard: Product lidstock contains the incorrect expiration date for the product
February 19, 2020Medical DevicesFDA
Arrow International Inc recalls EPIDURAL CATHETERIZATION KIT, Product Code BJC-05400-BEN
Hazard: There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.
February 19, 2020Medical DevicesFDA
Arrow International Inc recalls FlexTip Plus Epidural Catheterization Kit, Product Code YC-02220
Hazard: There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.
February 19, 2020Medical DevicesFDA
Arrow International Inc recalls EPIDURAL CATHETERIZATION KIT, Product Code UR-05501-FR1
Hazard: There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.
February 19, 2020Medical DevicesFDA
Arrow International Inc recalls EPIDURAL CATHETERIZATION KIT, Product Code UR-05501-EXP
Hazard: There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.
February 19, 2020Medical DevicesFDA
Arrow International Inc recalls EPIDURAL CATHETERIZATION KIT, Product Code UR-05501
Hazard: There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.
February 19, 2020Medical DevicesFDA
Arrow International Inc recalls Epidural Catheterization Kit with FlexTip Plus Catheter, Product Code TI-05520-EPI
Hazard: There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.
February 19, 2020Medical DevicesFDA
Arrow International Inc recalls FlexTip Plus Epidural Catheterization Kit, Product Code TI-05501-ME
Hazard: There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.
February 19, 2020Medical DevicesFDA
Arrow International Inc recalls FlexTip Plus Combined Spinal Epidural Catheterization Kit, Product Code NYU-05500-1
Hazard: There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.
February 19, 2020Medical DevicesFDA
Arrow International Inc recalls EPIDURAL CATHETERIZATION KIT, Product Code MTO-09903-KU
Hazard: There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.
February 19, 2020Medical DevicesFDA
Arrow International Inc recalls FlexTip Plus Epidural Catheterization Set, Product Code MTO-05500-TK
Hazard: There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.
February 19, 2020Medical DevicesFDA
Arrow International Inc recalls EPIDURAL CATHETERIZATION KIT, Product Code MTO-05500-SU
Hazard: There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.