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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 19, 2020Medical DevicesFDA
Arrow International Inc recalls FlexTip Plus Epidural Catheterization Kit, Product Code MP-17019-TKP
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 MP-17019-TIP
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 10 cc Luer-Slip Loss of Resistance Syringe, Product Code LR-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, Product Code JC-05400-LB
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 JC-05400-E
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 JC-05400-DCS
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 JC-05400-B
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 IT-05400-DC
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 FR-05501-12
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 FR-05501-10
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 FR-05501-04
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 for Pediatric Lumbar Placement, Product Code EC-05520-P
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 DE-05400D-BO
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 CZ-05400-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 CA-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 BE-080180-CHH
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 BE-080180-BXL
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 BE-05400-DCSHO
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 BE-05400-DCHH
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 BE-05400B-ETTEL
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 AT-05501-LIN
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 AT-05501-LEO
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 ASK-17019-MSC
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 ASK-05560-WH
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 ASK-05560-TG1
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 ASK-05503-BID
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, Open Tip, Single- Port Catheter, Product Code ASK-05502-NY
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 ASK-05501-SH
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 ASK-05400-CA1
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 ASK-05500-BID
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.