--- title: "AVID Medical, Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search AVID Medical, Inc. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/avid-medical-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # AVID Medical, Inc. recall records **147** reported ongoing 147 records in this archive. Latest source date Aug 10, 2026. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Aug 10, 2026 FDA device enforcement ### [Haylard 18G SINGLE SHOT EPI TRAY; Model/Item Number (Kit): DPGE002-02;](https://isitonrecall.com/recall/fda-device-z-3151-2026-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. Class I Reported ongoing Distribution: Domestic: IL, NC, VA, WY; [Official source for Haylard 18G SINGLE SHOT EPI TRAY; Model/Item Number (Kit): DPGE002-02;](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3151-2026%22) Aug 10, 2026 FDA device enforcement ### [Haylard CONTINUOUS NERVE BLOCK TRAY; Model/Item Number (Kit): BMCN001-05;](https://isitonrecall.com/recall/fda-device-z-3152-2026-haylard-continuous-nerve-block-tray-model-item-number-kit-bmcn001-05/) Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical. Class I Reported ongoing Distribution: Domestic: IL, NC, VA, WY; [Official source for Haylard CONTINUOUS NERVE BLOCK TRAY; Model/Item Number (Kit): BMCN001-05;](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3152-2026%22) Aug 10, 2026 FDA device enforcement ### [Haylard BASIC BIOPSY TRAY; Model/Item Number (Kit): PM415;](https://isitonrecall.com/recall/fda-device-z-3153-2026-haylard-basic-biopsy-tray-model-item-number-kit-pm415/) Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical. Class I Reported ongoing Distribution: Domestic: IL, NC, VA, WY; [Official source for Haylard BASIC BIOPSY TRAY; Model/Item Number (Kit): PM415;](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3153-2026%22) Aug 10, 2026 FDA device enforcement ### [Haylard UNIV IMAGING BIOPSY TRUCUSTOM; Model/Item Number (Kit): VARV042-03;](https://isitonrecall.com/recall/fda-device-z-3154-2026-haylard-univ-imaging-biopsy-trucustom-model-item-number-kit-varv042-03/) Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical. Class I Reported ongoing Distribution: Domestic: IL, NC, VA, WY; [Official source for Haylard UNIV IMAGING BIOPSY TRUCUSTOM; Model/Item Number (Kit): VARV042-03;](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3154-2026%22) Jul 14, 2026 FDA device enforcement ### [Halyard IV START KIT NON-STERILE REF: KRIV26-02](https://isitonrecall.com/recall/fda-device-z-3108-2026-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 Class I Reported ongoing Distribution: US Nationwide distribution in the state of NE. [Official source for Halyard IV START KIT NON-STERILE REF: KRIV26-02](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3108-2026%22) Jul 14, 2026 FDA device enforcement ### [Halyard IV Start Kit Non-Sterile REF: KRIV26-02](https://isitonrecall.com/recall/fda-device-z-3109-2026-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. Class II Reported ongoing Distribution: US Nationwide distribution in the state of NE. [Official source for Halyard IV Start Kit Non-Sterile REF: KRIV26-02](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3109-2026%22) Jul 10, 2026 FDA device enforcement ### [Halyard LAVH PACK, Model/Catalog Number: USAR053-11 containing Clearify Visualization System (5303907).](https://isitonrecall.com/recall/fda-device-z-2964-2026-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. Class II Reported ongoing Distribution: US Nationwide distribution in the state of TX. [Official source for Halyard LAVH PACK, Model/Catalog Number: USAR053-11 containing Clearify Visualization System (530...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2964-2026%22) Jul 9, 2026 FDA device enforcement ### [Brand Name: Halyard Product Name: DAVINCI TRUCUSTOM BUNDLE containing TRAY FOLEY 16FR W/STATLOCK Model/Catalog Number: SAMM064-27](https://isitonrecall.com/recall/fda-device-z-3005-2026-brand-name-halyard-product-name-davinci-trucustom-bundle-containing-tray-foley-16fr-w-statlock-model/) Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex. Class II Reported ongoing Distribution: US Nationwide distribution in the states of MS, TX. [Official source for Brand Name: Halyard Product Name: DAVINCI TRUCUSTOM BUNDLE containing TRAY FOLEY 16FR W/STATLOCK ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3005-2026%22) Jul 9, 2026 FDA device enforcement ### [Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03](https://isitonrecall.com/recall/fda-device-z-3006-2026-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. Class II Reported ongoing Distribution: US Nationwide distribution in the states of MS, TX. [Official source for Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3006-2026%22) Jul 9, 2026 FDA device enforcement ### [Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03](https://isitonrecall.com/recall/fda-device-z-3007-2026-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. Class II Reported ongoing Distribution: US Nationwide distribution in the states of MS, TX. [Official source for Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3007-2026%22) Jul 9, 2026 FDA device enforcement ### [Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03](https://isitonrecall.com/recall/fda-device-z-3008-2026-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. Class II Reported ongoing Distribution: US Nationwide distribution in the states of MS, TX. [Official source for Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3008-2026%22) Jul 9, 2026 FDA device enforcement ### [Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03](https://isitonrecall.com/recall/fda-device-z-3009-2026-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. Class II Reported ongoing Distribution: US Nationwide distribution in the states of MS, TX. [Official source for Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3009-2026%22) Jul 9, 2026 FDA device enforcement ### [Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03](https://isitonrecall.com/recall/fda-device-z-3010-2026-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. Class II Reported ongoing Distribution: US Nationwide distribution in the states of MS, TX. [Official source for Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3010-2026%22) Jul 9, 2026 FDA device enforcement ### [Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03](https://isitonrecall.com/recall/fda-device-z-3011-2026-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. Class II Reported ongoing Distribution: US Nationwide distribution in the states of MS, TX. [Official source for Halyard TOTAL JOINT Model/Catalog Number: MSBM036-03](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3011-2026%22) May 19, 2026 FDA device enforcement ### [Halyard STANDARD LINE INSERTION PACK. Model/Catalog Number: PVHM234-01. Convenience kit.](https://isitonrecall.com/recall/fda-device-z-2772-2026-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. Class II Reported ongoing Distribution: U.S. Nationwide distribution in the state of California. [Official source for Halyard STANDARD LINE INSERTION PACK. Model/Catalog Number: PVHM234-01. Convenience kit.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2772-2026%22) May 19, 2026 FDA device enforcement ### [Halyard medical convenience kits labeled as: 1) ENT, Model/Item Number (kit) ACEN89-01; 2) ENT, Model/Item Number (kit) ACEN89-02; 3) BACK PACK, Model/Item Number (kit) ALBK51-0...](https://isitonrecall.com/recall/fda-device-z-3044-2026-halyard-medical-convenience-kits-labeled-as-1-ent-model-item-number-kit-acen89-01-2-ent-model-item-n/) 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 variability of endotoxin levels on the prod... Class II Reported ongoing Distribution: US Nationwide distribution in the states of AZ, CA, CO, WA, WY, TX, MI, FL, MD, UT, NC, MS, PA, MO, IA, NE, OH, IL, SD, MN, GA. [Official source for Halyard medical convenience kits labeled as: 1) ENT, Model/Item Number (kit) ACEN89-01; 2) ENT, M...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3044-2026%22) May 19, 2026 FDA device enforcement ### [1) NEURO, (kit) ACNE73-01; 2) NEURO, (kit) ACNE73-03; 3) CRANI, (kit) AKCR19-01; 4) ORTHO SPINE PACK, (kit) ARMC017; 5) BMHM NEURO PACK, (kit) BMHT016-05; 6) LUMBAR PACK, (kit) ...](https://isitonrecall.com/recall/fda-device-z-3045-2026-1-neuro-kit-acne73-01-2-neuro-kit-acne73-03-3-crani-kit-akcr19-01-4-ortho-spine-pack-kit-armc017-5-b/) 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 variability of endotoxin levels on the prod... Class II Reported ongoing Distribution: US Nationwide distribution in the states of AZ, CA, CO, WA, WY, TX, MI, FL, MD, UT, NC, MS, PA, MO, IA, NE, OH, IL, SD, MN, GA. [Official source for 1) NEURO, (kit) ACNE73-01; 2) NEURO, (kit) ACNE73-03; 3) CRANI, (kit) AKCR19-01; 4) ORTHO SPINE P...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3045-2026%22) May 19, 2026 FDA device enforcement ### [Halyard medical convenience kits labeled as: 1) A-P PACK - 205936, Model/Item Number (kit) ANAP22-01; 2) POSTERIOR PACK - 205960, Model/Item Number (kit) ANPP15-01; 3) ANEURYSM ...](https://isitonrecall.com/recall/fda-device-z-3046-2026-halyard-medical-convenience-kits-labeled-as-1-a-p-pack-205936-model-item-number-kit-anap22-01-2-post/) 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 variability of endotoxin levels on the prod... Class II Reported ongoing Distribution: US Nationwide distribution in the states of AZ, CA, CO, WA, WY, TX, MI, FL, MD, UT, NC, MS, PA, MO, IA, NE, OH, IL, SD, MN, GA. [Official source for Halyard medical convenience kits labeled as: 1) A-P PACK - 205936, Model/Item Number (kit) ANAP22...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3046-2026%22) May 7, 2026 FDA device enforcement ### [Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit.](https://isitonrecall.com/recall/fda-device-z-2763-2026-halyard-eye-pack-model-catalog-number-lvey27-convenience-kit/) Incorrect concentration of Betadine solution contained within certain AVID convenience kits. Class II Reported ongoing Distribution: US Nationwide distribution in the state of California. [Official source for Halyard EYE PACK. Model/Catalog Number: LVEY27 Convenience kit.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2763-2026%22) Apr 30, 2026 FDA device enforcement ### [Halyard, Pain Pack. Kit Code: AMPK48-01.](https://isitonrecall.com/recall/fda-device-z-2407-2026-halyard-pain-pack-kit-code-ampk48-01/) Inadvertent distribution of sealed pouches that had not undergone validated sterilization. Class II Reported ongoing Distribution: US Nationwide distribution in the state of Iowa. [Official source for Halyard, Pain Pack. Kit Code: AMPK48-01.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2407-2026%22) ## Reasons in these listed records - Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical. - Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which are contaminated with Aspergillus penicillioides - 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. - The kit component was subjected to EO sterilization, contrary to the manufacturer recommendation, which may have led to the component leaking in a kit. These examples come from this result page and are not a ranking of every recall reason. ## Checking AVID Medical, Inc. ### Is there a recall on avid medical, inc. right now? This archive contains 147 records, including 147 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search AVID Medical, Inc.](https://isitonrecall.com/check/?q=AVID%20Medical%2C%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)