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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.
June 26, 2019Medical DevicesFDA
Arrow International Inc recalls Arrowg+ard Blue Advance" PICC pre loaded with Arrow¿ VPS" Precision Stylet Product Code: CDC 45041 VPS2
Hazard: Lidstock states the incorrect expiration date for the product
June 26, 2019Medical DevicesFDA
Arrow International Inc recalls Arrowg+ard Blue Advance PICC pre loaded with Arrow¿ VPS" Precision Stylet Product Code: CDC 44063 VPS2
Hazard: Lidstock states the incorrect expiration date for the product
June 26, 2019Medical DevicesFDA
Arrow International Inc recalls Arrowg+ard Blue Advance PICC pre loaded with Arrow¿ VPS" Precision Stylet Product Code: CDC 44052 VPS2
Hazard: Lidstock states the incorrect expiration date for the product
June 26, 2019Medical DevicesFDA
Arrow International Inc recalls Arrow¿ PICC with Chlorag+ard Technology Product Code: CDC 44052 HPK1A
Hazard: Lidstock states the incorrect expiration date for the product
June 26, 2019Medical DevicesFDA
Arrow International Inc recalls Arrow¿ JACC with Chlorag+ard¿ Technology Jugular Axillosubclavian Central Catheter Product Code
Hazard: Lidstock states the incorrect expiration date for the product
June 26, 2019Medical DevicesFDA
Arrow International Inc recalls Arrow¿ JACC with Chlorag+ard¿ Technology Jugular Axillo subclavian Central Catheter Product Code: CDC
Hazard: Lidstock states the incorrect expiration date for the product
June 26, 2019Medical DevicesFDA
Arrow International Inc recalls Arrow JACC with Chlorag+ard Technology Jugular Axillo subclavian Central Catheter Product Code:
Hazard: Lidstock states the incorrect expiration date for the product
June 26, 2019Medical DevicesFDA
Arrow International Inc recalls Arrowg+ard Blue Advance JACC Product Code: CDC 42063 JX1A
Hazard: Lidstock states the incorrect expiration date for the product
June 26, 2019Medical DevicesFDA
Arrow International Inc recalls Arrowg+ard Blue Advance JACC Product Code:CDC 42052 JX1A
Hazard: Lidstock states the incorrect expiration date for the product
June 26, 2019Medical DevicesFDA
Arrow International Inc recalls Arrowg+ard Blue Advance JACC Product Code: CDC 42041 JX1A
Hazard: Lidstock states the incorrect expiration date for the product
June 26, 2019Medical DevicesFDA
Arrow International Inc recalls Arrowg+ard Blue Advance JACC Product Code: CDC 41552 JX1A
Hazard: Lidstock states the incorrect expiration date for the product
June 26, 2019Medical DevicesFDA
Arrow International Inc recalls Arrowg+ard Blue Advance JACC Product Code: CDC 41541 JX1A
Hazard: Lidstock states the incorrect expiration date for the product
June 26, 2019Medical DevicesFDA
Arrow International Inc recalls Arrow PICC with Chlorag+ard Technology Product Code: CDA 45552 VPS2
Hazard: Lidstock states the incorrect expiration date for the product
June 26, 2019Medical DevicesFDA
Arrow International Inc recalls Arrow PICC with Chlorag+ard Technology Product Code: CDA 45541 HPK1A
Hazard: Lidstock states the incorrect expiration date for the product
June 26, 2019Medical DevicesFDA
Arrow International Inc recalls Arrow PICC with Chlorag+ard Technology Product Code: CDA 45052 HPK1A
Hazard: Lidstock states the incorrect expiration date for the product
June 26, 2019Medical DevicesFDA
Arrow International Inc recalls Arrow PICC with Chlorag+ard Technology Product Code: CDA 45041 HPK1A
Hazard: Lidstock states the incorrect expiration date for the product
June 26, 2019Medical DevicesFDA
Arrow International Inc recalls Arrow PICC with Chlorag+ard Technology Product Code: CDA 44052 HPK1A
Hazard: Lidstock states the incorrect expiration date for the product
June 26, 2019Medical DevicesFDA
Arrow International Inc recalls Arrow PICC Kit Product Code: ASK 45552 RWJ4
Hazard: Lidstock states the incorrect expiration date for the product
June 26, 2019Medical DevicesFDA
Arrow International Inc recalls Arrow PICC Kit pre loaded with Arrow¿ VPS Precision Stylet Product Code: ASK 45552 CRM
Hazard: Lidstock states the incorrect expiration date for the product
June 26, 2019Medical DevicesFDA
Arrow International Inc recalls Arrow PICC Kit Product Code: ASK 45541 RWJ4
Hazard: Lidstock states the incorrect expiration date for the product
June 26, 2019Medical DevicesFDA
Arrow International Inc recalls Arrow¿ PICC Kit Product Code: ASK 45541 LVH1
Hazard: Lidstock states the incorrect expiration date for the product
June 26, 2019Medical DevicesFDA
Arrow International Inc recalls Arrow PICC powered by Arrow VPS Stylet Product Code: ASK45041JHVA
Hazard: Lidstock states the incorrect expiration date for the product
May 22, 2019Medical DevicesFDA
Arrow International Inc recalls Arrow PICC powered by Arrow VPS Precision Stylet Product Code:CDC-44052-VPS2 Product Usage: The Arrow Pressure Inje
Hazard: Kits labeled as containing a 40 cm PICC may contain a 50 cm PICC, and kits labeled as containing a 50 cm PICC may contain a 40 cm PICC
May 22, 2019Medical DevicesFDA
Arrow International Inc recalls Arrow PICC powered by Arrow VPS Precision Stylet Product Code:CDC-45052-VPS2 Product Usage: The Arrow Pressure Inje
Hazard: Kits labeled as containing a 40 cm PICC may contain a 50 cm PICC, and kits labeled as containing a 50 cm PICC may contain a 40 cm PICC
April 17, 2019Medical DevicesFDA
Arrow International Inc recalls Arrow¿ Two-Lumen Central Venous Catheterization Set with Blue FlexTip¿ Catheter Product Code: CD-10802 GTN: 0080190
Hazard: The product lidstock contains a labelling error. The lidstock states the incorrect priming volume. The priming volumes printed on the extension lines are correct
April 17, 2019Medical DevicesFDA
Arrow International Inc recalls Arrow¿ Two-Lumen Central Venous Catheterization Kit with Blue FlexTip¿ Catheter Product Code: AH-11802 (OUS) GTN: 00
Hazard: The product lidstock contains a labelling error. The lidstock states the incorrect priming volume. The priming volumes printed on the extension lines are correct
March 6, 2019Medical DevicesFDA
Arrow International Inc recalls AF w/AS 550 x 1-14ML/HR 5ML-60LO CPNB, Product code MVBX60XL CPNB, Arrow AutoFuser Disposable Pain Control Pump
Hazard: Possible cracks on the body of the fill port connector, which may result in a leak. If the leak is identified while the user is filling the pump, there may be a delay while an alternative pump is located. If the leak goes undetected it may result in a reduced level of drug delivery to the patient and consequently a lower level of pain relief than that prescribed or expected. This may result in the need for other, additional analgesic drug administration.
March 6, 2019Medical DevicesFDA
Arrow International Inc recalls AF w/AS 550 x 1-14ML/HR 2ML-30LO CPNB, Product code MVBT30XL CPNB, Arrow AutoFuser Disposable Pain Control Pump
Hazard: Possible cracks on the body of the fill port connector, which may result in a leak. If the leak is identified while the user is filling the pump, there may be a delay while an alternative pump is located. If the leak goes undetected it may result in a reduced level of drug delivery to the patient and consequently a lower level of pain relief than that prescribed or expected. This may result in the need for other, additional analgesic drug administration.
March 6, 2019Medical DevicesFDA
Arrow International Inc recalls AF w/AS 550 x 1-14ML/HR 2ML-15LO CPNB, Product code MVBT15XL-CPNB, Arrow AutoFuser Disposable Pain Control Pump
Hazard: Possible cracks on the body of the fill port connector, which may result in a leak. If the leak is identified while the user is filling the pump, there may be a delay while an alternative pump is located. If the leak goes undetected it may result in a reduced level of drug delivery to the patient and consequently a lower level of pain relief than that prescribed or expected. This may result in the need for other, additional analgesic drug administration.
March 6, 2019Medical DevicesFDA
Arrow International Inc recalls AF w/AS 550 x 1-14 ml/hr, 5ml30 LOCPNB, Product code MVBX30XLCPNB, Arrow AutoFuser Disposable Pain Control Pump
Hazard: Possible cracks on the body of the fill port connector, which may result in a leak. If the leak is identified while the user is filling the pump, there may be a delay while an alternative pump is located. If the leak goes undetected it may result in a reduced level of drug delivery to the patient and consequently a lower level of pain relief than that prescribed or expected. This may result in the need for other, additional analgesic drug administration.