Drugs & medicalClass I

AVID Medical, Inc. recalls Halyard CARDIAC CATH TRAY SHANDS JAX kit. Model Number: SHND401-04, SHND401-05.

Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

Read the official notice →
Date
2026-05-13
Country
United States
Brand
AVID Medical
Product
Halyard CARDIAC CATH TRAY SHANDS JAX kit. Model Number: SHND401-04, SHND401-05.
Classification
Class I
Units
US distribution to FL, IL, MO, MS, NC, NE, TX.
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 Details may be shortened or out of date; the official notice is the authoritative source.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 AVID Medical recalls

  1. 2026-07-29
  2. US
    Drugs & medicalClass II

    AVID Medical, Inc. recalls Halyard STANDARD LINE INSERTION PACK. Model/Catalog Number: PVHM234-01. Convenience kit.

    Defects in the silicone seal, which may result in "doming" of the silicone seal due to improper sealing, potentially leading to fluid occlusion or leakage.

    FDA · DeviceAVID Medical, Inc.U.S. Nationwide distribution in the state of California.Official notice →
  3. US
    Drugs & medicalClass II

    AVID Medical, Inc. recalls Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit.

    Incorrect concentration of Betadine solution contained within certain AVID convenience kits.

    FDA · DeviceAVID Medical, Inc.US Nationwide distribution in the state of California.Official notice →
  4. 2026-06-17
  5. US
    Drugs & medicalClass II

    AVID Medical, Inc. recalls Halyard, Towel Six Pack. Kit Code: AMTS70-01.

    Inadvertent distribution of sealed pouches that had not undergone validated sterilization.

    FDA · DeviceAVID Medical, Inc.US Nationwide distribution in the state of Iowa.Official notice →
  6. 2026-02-18
  7. US
    Drugs & medicalClass II

    AVID Medical, Inc. recalls Halyard TRANSPORT BAG KIT. Kit Code: LIFE0080-01.

    Tyvek bag seal issue which may compromise sterility of the kit.

    FDA · DeviceAVID Medical, Inc.US Nationwide distribution in the states of New Jersey.Official notice →
  8. 2026-01-14
  9. US
    Drugs & medicalClass I

    AVID Medical, Inc. recalls Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOF1000-17.

    Devices are not suitable for organ transplant.

    FDA · DeviceAVID Medical, Inc.US Nationwide distribution in the states of FL, GA and Puerto Rico.Official notice →
  10. 2025-12-24
  11. US
    Drugs & medicalClass II

    AVID Medical, Inc. recalls Halyard, MIDTOWN GENERAL ARTERIOGRAM. Catalog Number: EUHM009-01.

    Potential for incomplete seal on header bag.

    FDA · DeviceAVID Medical, Inc.US distribution to GA, IL, NE, MD.Official notice →
All 21 AVID Medical recalls →

Other drugs & medical recalls in the United States

  1. 2026-05-13
  2. US
    Drugs & medicalClass II

    Intuitive Surgical, Inc. recalls Brand Name: Da Vinci X and Da Vinci Xi Product Name: da Vinci X, Xi Surgical System Model/Catalog Number: IS4000; IS4200 Software…

    Due to manipulator containing screws with in the arm sub-assembly that my be susceptible to breaking.

    FDA · DeviceIntuitive Surgical, Inc.Worldwide - U.S. Nationwide distribution including in the states of AK, AL,…Official notice →
  3. US
    Drugs & medicalClass I

    Medical Action Industries, Inc. 306 recalls Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case

    Convenience kit contains a syringe in which the rotating adapter may unwind during use, resulting in a loose connection and/or full disconnection between the syringe and manifold"

    FDA · DeviceMedical Action Industries, Inc. 306US distribution to state of: AZ OUS: NoneOfficial notice →
  4. US
    Drugs & medicalClass I

    American Contract Systems Inc recalls Convenience kits containing Medline Namic Angiographic Control Syringes with Rotating Adaptor CORONARY ANGIO PACK Model numbers…

    Impacted kits contain syringes recalled by Medline Industries. Syringe rotating adaptor may unwind during use, which may result in a loose connection or full disconnection between the syringe and manifold. Potential…

    FDA · DeviceAmerican Contract Systems IncUS distribution to MN. No OUS distribution.Official notice →
  5. US
    Drugs & medicalClass I

    Ventec Life Systems, Inc. recalls VOCSN V+Pro package, REF: PRT-01198-000; VOCSN V+Pro unit, REF: PRT-01185-000

    Respiratory system intended to provide continuous/intermittent ventilator support, may not have been evaluated under all intended high-pressure conditions during production testing, so an oxygen leak condition could…

    FDA · DeviceVentec Life Systems, Inc.US: OH, GA, CA, MOOfficial notice →
  6. US
    Drugs & medicalClass I

    Cook Incorporated recalls Centimeter Sizing Catheter RPN N5.0-35-100-P-10S-PIG-CSC-20 GPN G11916 Catheters for use in angiographic procedures are available in a…

    Marker bands may be at an increased risk of cracking/breakage. Potential adverse events that may result include increased procedural time, harms associated with device fragmentation/separation, and vessel injury. In a…

    FDA · DeviceCook IncorporatedUS distribution nationwide. OUS distribution to Brunei, Brazil, Canda, China,…Official notice →
  7. US
    Drugs & medicalClass I

    Intuitive Surgical, Inc. recalls Intuitive 8 mm SureForm 30 Gray Reloads Reference Numbers: 48230M-05 and 48230M-06

    Reloads for curved-tipped stapler may potentially produce an incomplete staple line.

    FDA · DeviceIntuitive Surgical, Inc.US: Alabama Alaska Arizona Arkansas California Colorado Connecticut Delaware…Official notice →
See all drugs & medical recalls →