AVID Medical, Inc. recalls
Every recall we track for AVID Medical, Inc. — 202 in all, from 2017–2026 — plus the complaints and injury reports the public filed about them. 15 are rated “stop using now”.
Recalls per year, by danger level
Recalls from AVID Medical, Inc. peaked in 2024 (73); 202 since 2017. 7% rated “stop using now”.
All FDA recall records for AVID Medical, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 4 | 19 | 1 | 24 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 1 | 8 | 0 | 0 | 9 |
| 2021 | 0 | 2 | 2 | 0 | 4 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 11 | 49 | 12 | 1 | 73 |
| 2025 | 2 | 0 | 34 | 1 | 37 |
| 2026 (to date) | 1 | 9 | 28 | 17 | 55 |
Most common reasons for AVID Medical, Inc. recalls
What to do if you have a recalled AVID Medical, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All AVID Medical, Inc. recalls
25 shown- UnratedMedical device
AVID Medical, Inc. recalls ROBOTIC PROSTATECTOMY PACK; Model/Item Number (Kit): NAMC423-11;
AVID Medical recalls 6 units of Robotic Prostatectomy Pack (Model NAMC423-11) due to potential lubricant contamination during manufacturing. Affected units were distributed nationwide in AZ, CA, FL, MD, NE, TX.
AVID MedicalAug 10, 2026 - Lower riskMedical device
AVID Medical, Inc. recalls Haylard BASIC BIOPSY TRAY; Model/Item Number (Kit): PM415;
AVID Medical recalls Haylard Basic Biopsy Trays with model PM415 due to potential sterility issues with sodium chloride ampules. Affected kits may not be safe for medical use.
AVID MedicalAug 10, 2026 - Lower riskMedical device
AVID Medical, Inc. recalls Halyard IV START KIT NON-STERILE; 48 kits per case. Containing BD ChloraPrep Clear - 1 mL Applicator. Kit Model Number:
AVID Medical recalls Halyard IV Start Kits with possible open seals on BD ChloraPrep applicators. Affected kits may have packaging that doesn't seal properly, risking contamination. Stop using immediately if you own these kits.
AVID MedicalJul 22, 2026 - Lower riskMedical device
AVID Medical, Inc. recalls Halyard IV START KIT NON-STERILE; 48 kits per case. Containing BD ChloraPrep Clear - 1 mL Applicator. Kit Model Number:
AVID Medical recalls 48-unit Halyard IV Start Kits (model KRIV26-02) due to possible Aspergillus penicillioides contamination. Affected kits may cause infections if used improperly.
AVID MedicalJul 22, 2026 - Stop using nowMedical device
AVID Medical, Inc. recalls Halyard IV START KIT NON-STERILE REF: KRIV26-02
AVID Medical recalls Halyard IV Start Kit (non-sterile) with contaminated Aspergillus penicillioides in applicators. Stop using to prevent infection risks.
AVID MedicalJul 14, 2026 - Lower riskMedical device
AVID Medical, Inc. recalls Halyard IV Start Kit Non-Sterile REF: KRIV26-02
AVID Medical recalls Halyard IV Start Kit Non-Sterile REF: KRIV26-02 due to potential contamination from paper lidding wrinkles breaching seals. Affected units sold from 7/31/2026 with specific lot numbers.
AVID MedicalJul 14, 2026 - Lower riskMedical device
AVID Medical, Inc. recalls Halyard LAVH PACK, Model/Catalog Number: USAR053-11 containing Clearify Visualization System (5303907).
AVID Medical recalls Halyard LAVH PACK Model USAR053-11 with Clearify Visualization System (5303907) due to potential leakage after EO sterilization. Affected units have specific UDI/DI and lot numbers.
AVID MedicalJul 10, 2026 - Lower riskMedical device
AVID Medical, Inc. recalls Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03
AVID Medical recalls Halyard TOTAL JOINT Model MSBM036-03 due to latex in statlock component. Affected units may cause allergic reactions. Contact for remedy.
AVID MedicalJul 9, 2026 - Lower riskMedical device
AVID Medical, Inc. recalls 1) NEURO, (kit) ACNE73-01; 2) NEURO, (kit) ACNE73-03; 3) CRANI, (kit) AKCR19-01; 4) ORTHO SPINE PACK, (kit) ARMC017; 5)
AVID Medical recalls Ritmed Neurological Sponges (models 55992C-55998C) due to potential for unexpected endotoxin levels. Consumers should check product labels for model numbers and lot numbers.
AVID MedicalMay 19, 2026 - Lower riskMedical device
AVID Medical, Inc. recalls Halyard STANDARD LINE INSERTION PACK. Model/Catalog Number: PVHM234-01. Convenience kit.
AVID Medical recalls Halyard STANDARD LINE INSERTION PACK model PVHM234-01 due to silicone seal defects that may cause fluid leakage or occlusion. Affected units include specific lot numbers with expiration dates.
AVID MedicalMay 19, 2026 - Lower riskMedical device
AVID Medical, Inc. recalls Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit.
AVID Medical recalls Halyard EYE PACK convenience kits with model LVEY27 due to incorrect Betadine solution concentration. Affected units have specific lot numbers and expiration dates.
AVID MedicalMay 7, 2026 - Lower riskMedical device
AVID Medical, Inc. recalls Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Manifolds. SAMMC ANGIOGRAPHY
AVID Medical recalls Halyard convenience kits with Medline Namic Angiographic Star Off Handle Manifolds due to particulates that could enter blood circulation and cause blockages.
AVID MedicalApr 30, 2026 - Lower riskMedical device
AVID Medical, Inc. recalls Halyard, Towel Six Pack. Kit Code: AMTS70-01.
AVID Medical recalls Halyard Towel Six Pack Kit Code AMTS70-01 due to unsterilized pouches. Affected units may pose infection risks if used without proper sterilization.
AVID MedicalApr 30, 2026 - Use cautionMedical device
AVID Medical, Inc. recalls Halyard CARDIAC CATH TRAY SHANDS JAX kit. Model Number: SHND401-04, SHND401-05.
AVID Medical recalls Halyard CARDIAC CATH TRAY SHANDS JAX kits (models SHND401-04 and SHND401-05) due to potential risk of medline syringe rotating adaptor unwinding, which may cause loose or full disconnection between syringe and manifold.
AVID MedicalMar 13, 2026 - Lower riskMedical device
AVID Medical, Inc. recalls Halyard TRANSPORT BAG KIT. Kit Code: LIFE0080-01.
AVID Medical recalls Halyard Transport Bag Kit (Kit Code LIFE0080-01) due to potential sterility compromise. Affected units may not maintain sterile conditions during medical procedures.
AVID MedicalJan 2, 2026 - Lower riskMedical device
AVID Medical, Inc. recalls Halyard, MIDTOWN GENERAL ARTERIOGRAM. Catalog Number: EUHM009-01.
AVID Medical recalls Halyard Arteriogram (EUHM009-01) due to potential incomplete seal on header bag. Affected units may have safety risks during medical procedures.
AVID MedicalNov 14, 2025 - Stop using nowMedical device
AVID Medical, Inc. recalls Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOF1000-17.
AVID Medical recalls Halyard Organ Recovery Pack (Kit Code LLOF1000-17) due to being unsuitable for organ transplant procedures. Affected units have specific UDI and lot numbers.
AVID MedicalNov 11, 2025 - Lower riskMedical device
AVID Medical, Inc. recalls Halyard, ENT PACK. Model Number: JACK421-04. Convenience kit.
AVID Medical recalls ENT packs with model JACK421-04 due to potential open header bag seals that could compromise sterility. Affected units were sold from 2021 to 2027.
AVID MedicalAug 4, 2025 - Lower riskMedical device
AVID Medical, Inc. recalls GYN ROBOTIC PACK. Medical convenience kit.
AVID Medical recalls GYN ROBOTIC PACK kits due to discoloration from resterilization. Affected kits have specific model and lot numbers. No action is required as the hazard is cosmetic.
AVID MedicalJun 11, 2025 - Lower riskMedical device
AVID Medical, Inc. recalls Halyard CHRIST SUTURE KIT. General Procedure Tray Convenience Kit
AVID Medical recalls Halyard CHRIST Suture Kit (Model ADVC800-03) due to potential silicone coating removal during use. Affected units may have diminished performance.
AVID MedicalMar 31, 2025 - Stop using nowMedical device
AVID Medical, Inc. recalls Halyard KIT, SHOULDER - Medical convenience kits Model Number: ESJH014-06
AVID Medical recalls shoulder surgical kits with potential metal flakes causing surgical site reactions. Affected model ESJH014-06 may need replacement to prevent foreign body reactions.
AVID MedicalSep 20, 2024 - Use cautionMedical device
Avid Medical, Inc. recalls FISTULA ON-OFF KIT. Medical convenience kit, Avid Medical Part Number: MMTN020.
Avid Medical recalls FISTULA ON-OFF Kit (Part MMTN020) due to potential Aspergillus contamination from package breaches. Affected kits may need replacement to prevent infection risks.
Avid MedicalApr 9, 2021 - Use cautionMedical device
Avid Medical, Inc. recalls Custom procedure trays containing medical components needed to facilitate patient procedures and to perform minor and
Avid Medical recalls custom surgical procedure trays containing non-sterile surgical gowns that could cause infections during surgery. Affected items include specific model numbers and lot numbers sold between 2020-2022.
Avid MedicalFeb 18, 2020 - Lower riskMedical device
Avid Medical, Inc. recalls AVID Medical QA Pack AV10654-10
Avid Medical recalls QA Pack AV10654-10 due to swab sticks expiring before the kit's expiration date. Affected kits have specific lot numbers and expiration dates.
Avid MedicalJul 3, 2017 - Use cautionMedical device
Avid Medical, Inc. recalls AVID TruCustom DAVINCI PACK convenience kits, Item Code: ADVU037-09
Avid Medical recalls specific DAVINCI PACK convenience kits that may contain loose polypropylene foreign material, posing a potential risk during medical use.
Avid MedicalJun 22, 2017
AVID Medical, Inc. recall questions
How many recalls has AVID Medical, Inc. had?
202 recalls from AVID Medical, Inc. are on record with U.S. safety agencies, from 2017–2026.
What is the most recent AVID Medical, Inc. recall?
AVID Medical, Inc. recalls ROBOTIC PROSTATECTOMY PACK; Model/Item Number (Kit): NAMC423-11;, dated Aug 10, 2026. Every AVID Medical, Inc. recall is listed on this page, newest first.
Why are AVID Medical, Inc. products recalled?
The most common reasons on record: Potential for incomplete seal on header bag. (5); Devices are not suitable for organ transplant. (3); Potential for open header bag seals, compromising sterility. (2).
What should I do if I have a recalled AVID Medical, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new AVID Medical, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.