AVID Medical recalls
21 official recalls and safety alerts involving AVID Medical since 2024-11, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.
This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with AVID Medical or the relevant agency.
- 2026-10-14
USAVID 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 →- 2026-09-30
- US
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.
- US
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.
- 2026-09-23
- US
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.
- US
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
- 2026-09-16
- US
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.
- 2026-09-09
- US
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 → - 2026-09-02
- US
AVID Medical, Inc. recalls Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
- 2026-08-26
- US
AVID Medical, Inc. recalls Halyard LAVH PACK, Model/Catalog Number: USAR053-11 containing Clearify Visualization System (5303907).
The kit component was subjected to EO sterilization, contrary to the manufacturer recommendation, which may have led to the component leaking in a kit.
- 2026-08-12
- US
AVID Medical, Inc. recalls Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Manifolds. SAMMC ANGIOGRAPHY SAMM066-15
Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufacturer due to presence of particulates within fluid path of the Manifolds. Particulate within the fluid path…
FDA · DeviceAVID Medical, Inc.US Nationwide distribution in the states of NC and TX.Official notice → - 2026-07-29
- US
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 → - US
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 → - 2026-06-17
- US
AVID Medical, Inc. recalls Halyard, Towel Six Pack. Kit Code: AMTS70-01.
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
- 2026-05-13
- US
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.
- 2026-02-18
- US
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 → - 2026-01-14
- US
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 → - 2025-12-24
- US
AVID Medical, Inc. recalls Halyard, MIDTOWN GENERAL ARTERIOGRAM. Catalog Number: EUHM009-01.
Potential for incomplete seal on header bag.
- 2025-09-17
- US
AVID Medical, Inc. recalls Halyard, ENT PACK. Model Number: JACK421-04. Convenience kit.
Potential for open header bag seals, compromising sterility.
- 2025-08-13
- US
AVID Medical, Inc. recalls GYN ROBOTIC PACK. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
- 2025-05-21
- US
AVID Medical, Inc. recalls Halyard CHRIST SUTURE KIT. General Procedure Tray Convenience Kit
An issue with a raw material used to coat some surgical needles that may result in diminished performance and/or removal of some silicone needle coating during use.
- 2024-11-20
- US
AVID Medical, Inc. recalls Halyard KIT, SHOULDER - Medical convenience kits Model Number: ESJH014-06
Sponge forceps and towel clamps associated with small loose metal flakes potentially could detach from the components. Metal flakes on components may enter a patients surgical site undetected causing local reactions or…