Drugs & medicalClass I

AVID Medical, Inc. recalls Haylard 18G SINGLE SHOT EPI TRAY; Model/Item Number (Kit): DPGE002-02;

Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.

Read the official notice →
Date
2026-09-23
Country
United States
Brand
AVID Medical
Product
Haylard 18G SINGLE SHOT EPI TRAY; Model/Item Number (Kit): DPGE002-02;
Classification
Class I
Units
Domestic: IL, NC, VA, WY;
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 Details may be shortened or out of date; the official notice is the authoritative source.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. 2026-10-14
  2. US
    Drugs & medicalClass II

    AVID Medical, Inc. recalls ROBOTIC PROSTATECTOMY PACK; Model/Item Number (Kit): NAMC423-11;

    Product may be potentially contaminated with a lubricant used during the manufacturing process.

    FDA · DeviceAVID Medical, Inc.US Nationwide distribution in the states of AZ, CA, FL, MD, NE, TX.Official notice →
  3. 2026-09-30
  4. US
    Drugs & medicalClass II

    AVID Medical, Inc. recalls Halyard IV START KIT NON-STERILE; 48 kits per case. Containing BD ChloraPrep Clear - 1 mL Applicator. Kit Model Number: KRIV26-02

    Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may exhibit an open or incomplete seal on the packaging of the applicator.

    FDA · DeviceAVID Medical, Inc.US Nationwide distribution.Official notice →
  5. US
    Drugs & medicalClass I

    AVID Medical, Inc. recalls Halyard IV START KIT NON-STERILE; 48 kits per case. Containing BD ChloraPrep Clear - 1 mL Applicator. Kit Model Number: KRIV26-02.

    Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may be contaminated with Aspergillus penicillioides.

    FDA · DeviceAVID Medical, Inc.US Nationwide distribution.Official notice →
  6. 2026-09-23
  7. US
    Drugs & medicalClass I

    AVID Medical, Inc. recalls Halyard IV START KIT NON-STERILE REF: KRIV26-02

    Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which are contaminated with Aspergillus penicillioides

    FDA · DeviceAVID Medical, Inc.US Nationwide distribution in the state of NE.Official notice →
  8. 2026-09-16
  9. US
    Drugs & medicalClass II

    AVID Medical, Inc. recalls Halyard IV Start Kit Non-Sterile REF: KRIV26-02

    Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which lacks sterility assurance due to to wrinkles in the paper lidding which may breach the seal area.

    FDA · DeviceAVID Medical, Inc.US Nationwide distribution in the state of NE.Official notice →
  10. 2026-09-09
  11. US
    Drugs & medicalClass II

    AVID Medical, Inc. recalls Halyard medical convenience kits labeled as: 1) A-P PACK - 205936, Model/Item Number (kit) ANAP22-01; 2) POSTERIOR PACK - 205960,…

    The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998C due to potential for unexpected…

    FDA · DeviceAVID Medical, Inc.US Nationwide distribution in the states of AZ, CA, CO, WA, WY, TX, MI, FL,…Official notice →
All 21 AVID Medical recalls →

Other drugs & medical recalls in the United States

  1. 2026-09-23
  2. US
    Drugs & medicalClass II

    NOXBOX LTD recalls NOxBOXi Nitric Oxide Delivery System.

    Potential for oxygen tubing leaks due to failure of the tubing or tubing connection, which may lead to oxygen desaturation.

    FDA · DeviceNOXBOX LTDUS Nationwide distribution in the state of Georgia.Official notice →
  3. US
    Drugs & medicalClass II

    Nuclein LLC recalls Brand Name: DASH Rapid PCR Instrument Product Name: DASH Rapid PCR Instrument Model/Catalog Number: SG-0002 Software Version: 6.0.2,…

    Due to a software issue

    FDA · DeviceNuclein LLCUS Nationwide distribution in the states of Alabama, Delaware, Florida,…Official notice →
  4. US
    Drugs & medicalClass II

    ICU Medical, Inc. recalls Oncology sets with drip chambers

    Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material within the drip chamber wall that does not…

    FDA · DeviceICU Medical, Inc.Worldwide - US Nationwide distribution including in the states and territories…Official notice →
  5. US
    Drugs & medicalClass I

    Abiomed, Inc. recalls Automated Impella Controller (AIC) with the below product descriptions and corresponding Product Codes. 1. Impella Controller, Packaged,…

    The potential for purge cassette recognition issues due to the failure of the purge flag component of the purge pressure sensor assembly.

    FDA · DeviceAbiomed, Inc.Domestic: Nationwide Distribution. International: United Arab Emirates,…Official notice →
  6. US
    Drugs & medicalClass II

    Bayer Medical Care, Inc. recalls MEDRAD¿ Stellant FLEX Syringe Kit used with Stellant FLEX CT Injection System; Catalog number: FLEXS-150-QFT;

    Some devices may not have been properly sterilized due to a manufacturing sterilization issue.

    FDA · DeviceBayer Medical Care, Inc.US Nationwide distribution.Official notice →
  7. US
    Drugs & medicalClass II

    Maquet Cardiopulmonary Gmbh recalls Percutaneous Insertion Kit (PIK), Guidewire 100 cm, Model Numbers: 701053068 (USA), 701047384 (OUS);

    The packaging may not consistently maintain sterile barrier integrity.

    FDA · DeviceMaquet Cardiopulmonary GmbhWorldwide distribution - US Nationwide and the countries of Australia,…Official notice →
See all drugs & medical recalls →