FDA Class II · Medical device · October 14, 2026
ABD HYSTERECTOMY recall — AVID Medical, Inc.
Product may be potentially contaminated with a lubricant used during the manufacturing process.
Official ID Z-0106-2027 · Official record ↗
AVID Medical recalls
54 recent recalls on record for AVID Medical in connected official government data as of October 22, 2026 at 12:00 PM UTC.
Models with recalls
1) NEURO (1)ABD HYSTERECTOMY (1)ADULT HEART TRAY SHANDS JACKS (1)Brand Name (1)CRANIOTOMY PACK (1)DAVINCI LAP/GYN (1)DAVINCI TRUCUSTOM BUNDLE (1)ENDOVASCULAR PACK (1)GYN LAPAROSCOPY PACK (1)GYN LAPAROSCOPY/LAPAROTOMY (1)HEART PREP TRAY (1)Halyard (4)Halyard CARDIAC CATH PACK SAN23CARDQ kit (1)Halyard CARDIAC CATH PACK kit (1)Halyard CARDIAC CATH TRAY SHANDS JAX kit (1)Halyard CATH LAB kit (2)Halyard EYE PACK (1)Halyard HEART CATH (1)Halyard IV START KIT NON-STERILE (3)Halyard IV START KIT NON-STERILE REF (2)Halyard LAVH PACK (1)Halyard NEURO IR PERIPHERAL (PS 64405) kit (1)Halyard PERC TRAY kit (1)Halyard SAMMC ANGIOGRAPHY kit (1)Halyard STANDARD LINE INSERTION PACK (1)Halyard TOTAL JOINT Model/Catalog Number (6)Halyard VA DETROIT CATH LAB PACK kit (1)Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Ma (3)Halyard medical convenience kits labeled as (2)Haylard 18G SINGLE SHOT EPI TRAY (1)Haylard BASIC BIOPSY TRAY (1)Haylard CONTINUOUS NERVE BLOCK TRAY (1)Haylard UNIV IMAGING BIOPSY TRUCUSTOM (1)LAPAROSCOPIC PROSTATECTOMY (1)MAJOR PACK (1)PACK OPEN HEART CFH (1)PLASTICS TRAY (1)ROBOTIC PROSTATECTOMY PACK (1)UROLOGY MAJOR (1)
All AVID Medical recalls
FDA Class II · Medical device · October 14, 2026
GYN LAPAROSCOPY PACK recall — AVID Medical, Inc.
Product may be potentially contaminated with a lubricant used during the manufacturing process.
Official ID Z-0105-2027 · Official record ↗
FDA Class II · Medical device · October 14, 2026
MAJOR PACK recall — AVID Medical, Inc.
Product may be potentially contaminated with a lubricant used during the manufacturing process.
Official ID Z-0104-2027 · Official record ↗
FDA Class II · Medical device · October 14, 2026
UROLOGY MAJOR recall — AVID Medical, Inc.
Product may be potentially contaminated with a lubricant used during the manufacturing process.
Official ID Z-0103-2027 · Official record ↗
FDA Class II · Medical device · October 14, 2026
HEART PREP TRAY recall — AVID Medical, Inc.
Product may be potentially contaminated with a lubricant used during the manufacturing process.
Official ID Z-0102-2027 · Official record ↗
FDA Class II · Medical device · October 14, 2026
DAVINCI LAP/GYN recall — AVID Medical, Inc.
Product may be potentially contaminated with a lubricant used during the manufacturing process.
Official ID Z-0101-2027 · Official record ↗
FDA Class II · Medical device · October 14, 2026
PLASTICS TRAY recall — AVID Medical, Inc.
Product may be potentially contaminated with a lubricant used during the manufacturing process.
Official ID Z-0100-2027 · Official record ↗
FDA Class II · Medical device · October 14, 2026
LAPAROSCOPIC PROSTATECTOMY recall — AVID Medical, Inc.
Product may be potentially contaminated with a lubricant used during the manufacturing process.
Official ID Z-0099-2027 · Official record ↗
FDA Class II · Medical device · October 14, 2026
ROBOTIC PROSTATECTOMY PACK recall — AVID Medical, Inc.
Product may be potentially contaminated with a lubricant used during the manufacturing process.
Official ID Z-0098-2027 · Official record ↗
FDA Class II · Medical device · October 14, 2026
PACK OPEN HEART CFH recall — AVID Medical, Inc.
Product may be potentially contaminated with a lubricant used during the manufacturing process.
Official ID Z-0097-2027 · Official record ↗
FDA Class II · Medical device · October 14, 2026
CRANIOTOMY PACK recall — AVID Medical, Inc.
Product may be potentially contaminated with a lubricant used during the manufacturing process.
Official ID Z-0096-2027 · Official record ↗
FDA Class II · Medical device · October 14, 2026
ENDOVASCULAR PACK recall — AVID Medical, Inc.
Product may be potentially contaminated with a lubricant used during the manufacturing process.
Official ID Z-0095-2027 · Official record ↗
FDA Class II · Medical device · October 14, 2026
ADULT HEART TRAY SHANDS JACKS recall — AVID Medical, Inc.
Product may be potentially contaminated with a lubricant used during the manufacturing process.
Official ID Z-0094-2027 · Official record ↗
FDA Class II · Medical device · October 14, 2026
GYN LAPAROSCOPY/LAPAROTOMY recall — AVID Medical, Inc.
Product may be potentially contaminated with a lubricant used during the manufacturing process.
Official ID Z-0093-2027 · Official record ↗
FDA Class II · Medical device · October 14, 2026
DAVINCI TRUCUSTOM BUNDLE recall — AVID Medical, Inc.
Product may be potentially contaminated with a lubricant used during the manufacturing process.
Official ID Z-0092-2027 · Official record ↗
FDA Class II · Medical device · September 30, 2026
Halyard IV START KIT NON-STERILE recall — AVID Medical, Inc.
Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may exhibit an open or incomplete seal on the packaging of the applicator.
Official ID Z-3261-2026 · Official record ↗
FDA Class II · Medical device · September 30, 2026
Halyard IV START KIT NON-STERILE recall — AVID Medical, Inc.
Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may exhibit an open or incomplete seal on the packaging of the applicator.
Official ID Z-3260-2026 · Official record ↗
FDA Class I · Medical device · September 30, 2026
Halyard IV START KIT NON-STERILE recall — AVID Medical, Inc.
Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may be contaminated with Aspergillus penicillioides.
Official ID Z-3194-2026 · Official record ↗
FDA Class I · Medical device · September 23, 2026
Haylard UNIV IMAGING BIOPSY TRUCUSTOM recall — AVID Medical, Inc.
Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.
Official ID Z-3154-2026 · Official record ↗
FDA Class I · Medical device · September 23, 2026
Haylard BASIC BIOPSY TRAY recall — AVID Medical, Inc.
Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.
Official ID Z-3153-2026 · Official record ↗
FDA Class I · Medical device · September 23, 2026
Haylard CONTINUOUS NERVE BLOCK TRAY recall — AVID Medical, Inc.
Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.
Official ID Z-3152-2026 · Official record ↗
FDA Class I · Medical device · September 23, 2026
Haylard 18G SINGLE SHOT EPI TRAY recall — AVID Medical, Inc.
Potential for product quality and sterility issues regarding kits containing Sodium Chloride ampules subject to recall by Spectra Medical.
Official ID Z-3151-2026 · Official record ↗
FDA Class I · Medical device · September 23, 2026
Halyard IV START KIT NON-STERILE REF recall — AVID Medical, Inc.
Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which are contaminated with Aspergillus penicillioides
Official ID Z-3108-2026 · Official record ↗
FDA Class II · Medical device · September 16, 2026
Halyard IV Start Kit Non-Sterile REF recall — AVID Medical, Inc.
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 …
Official ID Z-3109-2026 · Official record ↗
FDA Class II · Medical device · September 9, 2026
Halyard medical convenience kits labeled as recall — AVID Medical, Inc.
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 55998…
Official ID Z-3046-2026 · Official record ↗
FDA Class II · Medical device · September 9, 2026
1) NEURO recall — AVID Medical, Inc.
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 55998…
Official ID Z-3045-2026 · Official record ↗
FDA Class II · Medical device · September 9, 2026
Halyard medical convenience kits labeled as recall — AVID Medical, Inc.
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 55998…
Official ID Z-3044-2026 · Official record ↗
FDA Class II · Medical device · September 2, 2026
Halyard TOTAL JOINT Model/Catalog Number recall — AVID Medical, Inc.
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
Official ID Z-3011-2026 · Official record ↗
FDA Class II · Medical device · September 2, 2026
Halyard TOTAL JOINT Model/Catalog Number recall — AVID Medical, Inc.
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
Official ID Z-3010-2026 · Official record ↗
FDA Class II · Medical device · September 2, 2026
Halyard TOTAL JOINT Model/Catalog Number recall — AVID Medical, Inc.
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
Official ID Z-3009-2026 · Official record ↗
FDA Class II · Medical device · September 2, 2026
Halyard TOTAL JOINT Model/Catalog Number recall — AVID Medical, Inc.
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
Official ID Z-3008-2026 · Official record ↗
FDA Class II · Medical device · September 2, 2026
Halyard TOTAL JOINT Model/Catalog Number recall — AVID Medical, Inc.
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
Official ID Z-3007-2026 · Official record ↗
FDA Class II · Medical device · September 2, 2026
Halyard TOTAL JOINT Model/Catalog Number recall — AVID Medical, Inc.
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
Official ID Z-3006-2026 · Official record ↗
FDA Class II · Medical device · September 2, 2026
Brand Name recall — AVID Medical, Inc.
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
Official ID Z-3005-2026 · Official record ↗
FDA Class II · Medical device · August 26, 2026
Halyard LAVH PACK recall — AVID Medical, Inc.
The kit component was subjected to EO sterilization, contrary to the manufacturer recommendation, which may have led to the component leaking in a kit.
Official ID Z-2964-2026 · Official record ↗
FDA Class I · Medical device · August 12, 2026
Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Ma recall — AVID Medical, Inc.
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 Manifol…
Official ID Z-2798-2026 · Official record ↗
FDA Class I · Medical device · August 12, 2026
Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Ma recall — AVID Medical, Inc.
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 Manifol…
Official ID Z-2797-2026 · Official record ↗
FDA Class I · Medical device · August 12, 2026
Halyard convenience kits containing recalled Medline Namic Angiographic Star Off Handle Ma recall — AVID Medical, Inc.
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 Manifol…
Official ID Z-2796-2026 · Official record ↗
FDA Class II · Medical device · July 29, 2026
Halyard STANDARD LINE INSERTION PACK recall — AVID Medical, Inc.
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.
Official ID Z-2772-2026 · Official record ↗
FDA Class II · Medical device · July 29, 2026
Halyard EYE PACK recall — AVID Medical, Inc.
Incorrect concentration of Betadine solution contained within certain AVID convenience kits.
Official ID Z-2763-2026 · Official record ↗
FDA Class II · Medical device · June 17, 2026
Halyard recall — AVID Medical, Inc.
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
Official ID Z-2410-2026 · Official record ↗
FDA Class II · Medical device · June 17, 2026
Halyard recall — AVID Medical, Inc.
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
Official ID Z-2409-2026 · Official record ↗
FDA Class II · Medical device · June 17, 2026
Halyard recall — AVID Medical, Inc.
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
Official ID Z-2408-2026 · Official record ↗
FDA Class II · Medical device · June 17, 2026
Halyard recall — AVID Medical, Inc.
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
Official ID Z-2407-2026 · Official record ↗
FDA Class I · Medical device · May 13, 2026
Halyard VA DETROIT CATH LAB PACK kit recall — AVID Medical, Inc.
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.
Official ID Z-1979-2026 · Official record ↗
FDA Class I · Medical device · May 13, 2026
Halyard SAMMC ANGIOGRAPHY kit recall — AVID Medical, Inc.
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.
Official ID Z-1978-2026 · Official record ↗
FDA Class I · Medical device · May 13, 2026
Halyard PERC TRAY kit recall — AVID Medical, Inc.
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.
Official ID Z-1977-2026 · Official record ↗
FDA Class I · Medical device · May 13, 2026
Halyard NEURO IR PERIPHERAL (PS 64405) kit recall — AVID Medical, Inc.
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.
Official ID Z-1976-2026 · Official record ↗
FDA Class I · Medical device · May 13, 2026
Halyard HEART CATH recall — AVID Medical, Inc.
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.
Official ID Z-1975-2026 · Official record ↗
FDA Class I · Medical device · May 13, 2026
Halyard CATH LAB kit recall — AVID Medical, Inc.
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.
Official ID Z-1974-2026 · Official record ↗
FDA Class I · Medical device · May 13, 2026
Halyard CATH LAB kit recall — AVID Medical, Inc.
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.
Official ID Z-1973-2026 · Official record ↗
FDA Class I · Medical device · May 13, 2026
Halyard CARDIAC CATH TRAY SHANDS JAX kit recall — AVID Medical, Inc.
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.
Official ID Z-1972-2026 · Official record ↗
FDA Class I · Medical device · May 13, 2026
Halyard CARDIAC CATH PACK SAN23CARDQ kit recall — AVID Medical, Inc.
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.
Official ID Z-1971-2026 · Official record ↗
FDA Class I · Medical device · May 13, 2026
Halyard CARDIAC CATH PACK kit recall — AVID Medical, Inc.
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.
Official ID Z-1970-2026 · Official record ↗
Verify with the official sources:
- CPSC — consumer products ↗ (aggregated here)
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- FDA — food, drugs, medical devices ↗ (aggregated here)
- USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
- Recalls.gov — the U.S. government’s all-agency portal ↗
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Compiled from official public-domain government data. Last checked October 22, 2026 at 12:00 PM UTC.