Drugs & medicalClass I

ARROW INTERNATIONAL, LLC recalls Description/REF: PI JACC KIT: 2L 5.5 FR X 15 CM CG+/ASK-41552-LTAC; PI JACC KIT: 3L 6 FR X 20 CM CG+/ASK-42063-LTAC; AGBA PI JACC KIT:…

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if…

Read the official notice →
Date
2026-06-24
Country
United States
Brand
Arrow
Product
Description/REF: PI JACC KIT: 2L 5.5 FR X 15 CM CG+/ASK-41552-LTAC; PI JACC KIT: 3L 6 FR X 20 CM CG+/ASK-42063-LTAC; AGBA PI JACC KIT: 1-L…
Classification
Class I
Units
US Nationwide distribution including in the states of VA, NY, UT, SC, LA, MN,…
Category
Drugs & medical
Source
FDA · Device

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

More Arrow recalls

  1. 2026-05-20
  2. US
    Drugs & medicalClass I

    ARROW INTERNATIONAL, LLC recalls Arrow-Clark VectorFlow Antegrade Chronic Hemodialysis Catheter: REF: ACS-15192-VFI, ACS-15232-VFI, ACS-15272-VFI, CS-15192-VFI,…

    16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer may not split as intended, and may result in withdrawal resistance,…

    FDA · DeviceARROW INTERNATIONAL, LLCWorldwide distribution: US nationwide and countries of: AE, AL, AR, AT, AU,…Official notice →
  3. 2026-04-29
  4. US
    Drugs & medicalClass II

    ARROW INTERNATIONAL, LLC recalls MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters REF ASK-11142-LC2 UDI code:…

    Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured

    FDA · DeviceARROW INTERNATIONAL, LLCU.S. Nationwide distribution in the states of AZ, CA, GA, MA, ME, MI, OR, PA,…Official notice →
  5. US
    Drugs & medicalClass II

    ARROW INTERNATIONAL, LLC recalls Arrow Echogenic Introducer Needle REF ASK-04001-BWK2 UDI code: (01)10801902220315(17)261231(11)251210(10)33F25J0347 This device is…

    Due to receiving a notice from a supplier that the liquid adhesive were incorrectly manufactured

    FDA · DeviceARROW INTERNATIONAL, LLCU.S. Nationwide distribution in the states of AZ, CA, GA, MA, ME, MI, OR, PA,…Official notice →
  6. 2024-10-02
  7. US
    Drugs & medicalClass II

    ARROW INTERNATIONAL Inc. recalls Arrow Arterial Kits and Trays as follows: (1) Arrow Arterial Access Tray with 0.025" Spring-Wire Guide (Catheter Not Included), REF…

    Reports have been received regarding open seals on the packaging.

    FDA · DeviceARROW INTERNATIONAL Inc.US Nationwide distribution in the states of CA, FL, GA, IL, MA, ME, MI, NC,…Official notice →
  8. 2024-06-12
  9. US
    Drugs & medicalClass I

    ARROW INTERNATIONAL Inc. recalls Arrow FiberOptix Intra-Aortic Balloon Catheter Kit: a) REF IAB-05830-LWS; b) REF IAB-05840-LWS; c) REF IAB-05850-LWS

    Teleflex received reports indicating an infrequent condition that, when not identified and corrected promptly, could result in serious health consequences. The issue may manifest as: -failure of the intra-aortic…

    FDA · DeviceARROW INTERNATIONAL Inc.Worldwide distribution. US nationwide including Puerto Rico, AU, BA, BE, BG,…Official notice →
  10. 2024-03-27
  11. US
    Drugs & medicalClass I

    ARROW INTERNATIONAL Inc. recalls ARROW QuickFlash Radial Artery Catherization (wire, guide, catheter), Part Numbers: a) REF AK-04220; b) REF ASK-04220-FMH1; c) REF…

    Teleflex is initiating this voluntary recall for the above-mentioned products due to reports received indicating a potentially defective component. The complaints received relate to resistance of the guidewire…

    FDA · DeviceARROW INTERNATIONAL Inc.Worldwide distribution: US (nationwide) and OUS (foreign) to countries of: AE,…Official notice →
All 15 Arrow recalls →

Other drugs & medical recalls in the United States

  1. 2026-06-24
  2. US
    Drugs & medicalClass II

    Steris Corporation recalls HarmonyAIR A-Series Surgical Lighting System

    There is a potential for paint delamination (chipping/peeling) on the lighting system's light heads.

    FDA · DeviceSteris CorporationWorldwide distribution - US Nationwide and the countries of Australia, Canada,…Official notice →
  3. US
    Drugs & medicalClass II

    Medline Industries, LP recalls Medline convenience kits: CMH CENTRAL LINE DRESSING CHANGE KIT EBSI1705A CVC/PICC/MIDLINE DRESSING CHANGE KIT EBSI1057A DIALYSIS DRESSING…

    Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

    FDA · DeviceMedline Industries, LPUS Nationwide distribution. OUS distribution pending.Official notice →
  4. US
    Drugs & medicalClass II

    PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls Philips MultiDiagnost Eleva with the following Model Numbers: Model # 708032 for MultiDiagnost Eleva; Model # 708034 for…

    Philips Allura Xper and MultiDiagnost-Eleva systems Hand switch button not fully releasing potentially leading to loss of imaging functionality or unintended radiation exposure and additional contrast injection

    FDA · DevicePHILIPS MEDICAL SYSTEMS NEDERLAND B.V.US and ROW.Official notice →
  5. US
    Drugs & medicalClass I

    Abiomed, Inc. recalls Automated Impella Controller (AIC), for use with left heart support blood pump. Labeled as the following with corresponding Product Codes:…

    Potential software error in the Automated Impella Controller ("AIC" ) when used in conjunction with left ventricular Impella devices.

    FDA · DeviceAbiomed, Inc.Worldwide distribution - US Nationwide and the countries of Australia,…Official notice →
  6. US
    Drugs & medicalClass I

    Datex-Ohmeda Inc recalls Giraffe Stand-alone Infant Resuscitation System; Powered emergency ventilator (resuscitator) Product identifiers: 2082663-001,…

    Blender knob shaft can loosen, which can affect the delivered oxygen concentration. The system can deliver an oxygen concentration that does not match the intended concentration set by the user, potentially resulting…

    FDA · DeviceDatex-Ohmeda IncPendingOfficial notice →
  7. US
    Drugs & medicalClass II

    Dabur India Limited recalls Med Pride, HYDROCORTISONE CREAM 1%, Net Wt. 1 oz (28.3g) tubes, Manufactured for: Shield Line LLC, 59 Hook Road, Bayonne, NJ 07002 USA,…

    CGMP Deviations; deficiencies observed during FDA inspection

    FDA · DrugDabur India LimitedUS Nationwide.Official notice →
See all drugs & medical recalls →