Every recall we track for AVID Medical, Inc. — 175 in all — plus the complaints and injury reports the public filed about them.
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 Medical recalls Halyard TOTAL JOINT Model MSBM036-03 due to latex in statlock component. Affected units may cause allergic reactions. Contact for remedy.
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 Medical recalls Halyard TOTAL JOINT Model MSBM036-03 due to latex in statlock component. Affected units may cause allergic reactions. Contact for remedy.
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 Medical recalls Halyard TOTAL JOINT Model MSBM036-03 due to latex in statlock component. Affected units may cause allergic reactions. Contact for remedy.
Halyard recalls DAVINCI TRUCUSTOM BUNDLE containing TRAY FOLEY 16FR with statlock due to latex labeling deficiency. Affected units may cause allergic reactions.
AVID Medical recalls Halyard TOTAL JOINT Model MSBM036-03 due to latex in statlock component. Affected units may cause allergic reactions. Contact for replacement.
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 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 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 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 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 Medical recalls Halyard Eye Bag Pack (Kit Code UIEB48-01) due to unsterilized pouches that could pose infection risks. Affected units include specific lot numbers and expiration dates.
AVID Medical recalls Halyard Drape Pack Kit (Code LMDP36-01) due to unsterilized pouches. Affected units may pose infection risks if used.
AVID Medical recalls Halyard Pain Pack Kit Code AMPK48-01 due to unsterilized pouches. Affected units may pose infection risks if used without proper sterilization.
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 Medical recalls Halyard PERC TRAY kits (models SLPC34-01, SLPC34-02) due to potential syringe disconnection during use. Affected units have specific lot numbers.
AVID Medical recalls Halyard SAMMC Angiography kit model SAMM066-15 due to potential risk of syringe rotating adaptor unwinding, causing loose or full disconnection between syringe and manifold.
AVID Medical recalls Halyard HEART CATH SELF REGIONAL kit (model SELF131-05) due to potential syringe disconnection during use. Affected units have specific lot numbers.
AVID Medical recalls Halyard NEURO IR Peripheral (PS 64405) kits with model UINR44-01 due to potential risk of syringe rotating adaptor unwinding, causing loose connections or disconnections during use.
AVID Medical recalls Halyard Cath Lab kit (model SACL75AM) due to potential syringe disconnection during use. Affected units have specific lot numbers.
AVID Medical recalls Halyard CARDIAC CATH PACK kits with model EAMC1000-05 or WAFB208-02 due to potential syringe disconnection during use. Affected units may have loose connections causing medical issues.
AVID Medical recalls Halyard Cath Lab kit model SACL75-01 due to potential syringe disconnection during use. Affected units have specific UDI lot numbers.
AVID Medical recalls Halyard VA Detroit Cath Lab Pack kit (model VMCD029) due to potential syringe disconnection during use. Affected units may cause medical complications if not addressed.
AVID Medical recalls Halyard CARDI:AC CATH PACK SAN23CARDQ kit (model DRCC36) due to potential loose connections from syringe rotating adaptor unwinding during use.
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 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 Medical recalls Halyard General Laparoscopy Pack (VAST018-10) due to potential incomplete seal on header bag. This could lead to leaks during surgery. Affected units have specific catalog and lot numbers.
AVID Medical recalls Halyard head and neck trays with catalog number EURO016-09 due to potential incomplete seal on header bag. This could affect safety during medical procedures.
AVID Medical recalls Halyard Major Pack (Catalog JEMJ10-01) due to potential incomplete seal on header bag. Affected units may have a risk of improper sealing.
AVID Medical recalls Halyard EP LAB PK (Catalog ESJH009-03) due to potential incomplete seal on header bag. This could affect product integrity but no specific injury risk is mentioned.
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 Medical recalls Halyard MINI PLUS Kit South (Kit Code JACK097-08) due to being unsuitable for organ transplant procedures. Affected units have specific identifiers.
AVID Medical recalls Halyard Organ Recovery Pack (Kit Code LLOG1000-15) due to being unsuitable for organ transplant. Affected units have specific lot numbers and UDI.
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 Medical recalls Halyard CPT BASIC IR PACK model 1646381 due to potential open header bag seals compromising sterility. Affected units sold until January 2028.
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 Medical recalls DA VINCI PACK URO/PROSTATE medical kits due to discoloration from resterilization. Affected kits have model VAHT009-19 and lot number 1579555.
AVID Medical recalls CT DAVINCI medical convenience kits with discoloration due to resterilization. Affected kits may have visual issues; contact for details.
AVID Medical recalls GS Endoscopy Packs (models NAMC421-10 to NAMC421-12) due to discoloration from resterilization. Affected kits may have visual issues during procedures.
AVID Medical recalls DAVINCI Urology medical convenience kits with model numbers WRNM038-09 to WRNM038-11 due to discoloration from resterilization.
AVID Medical recalls Cardiac Robot Pack kits with model RYCB72-03 that may discolor due to resterilization. Affected kits were sold in 2023.
AVID Medical recalls specific General Robotic Packs due to discoloration from resterilization. Affected kits may have visual issues but pose no safety risk. Contact for details.
AVID Medical recalls HVI CARDIAC ROBOT PACK medical kits due to discoloration from resterilization. Affected kits may have visual issues but no injury risk.
AVID Medical recalls partial nephrectomy packs due to discoloration from resterilization. Affected kits have specific model numbers and lot codes. Consumers should contact for details.
AVID Medical recalls specific thoracoscopy basin kits due to discoloration from resterilization. Affected kits have model numbers NIHB0022-09 to NIHB0022-12 and specific lot numbers.
AVID Medical recalls specific LAPAROSCOPY PACK kits due to discoloration from resterilization. Affected kits have model numbers VAML025-05 and WRNM007-15. No action is required as the issue is cosmetic.
AVID Medical recalls GEN LAPAROS: Kits with discoloration from resterilization. Affected kits have specific model numbers and lot codes. No action needed for safety.
AVID Medical recalls specific laparoscopy trays due to discoloration from resterilization. Affected models include EURO010-08 and USAR042-17. No action needed as discoloration is cosmetic.
AVID Medical recalls robotic prostatectomy packs with discoloration from resterilization. Affected kits may have visual issues during surgery.
AVID Medical recalls GYN Laparoscopy Packs (model NAFB055-08, NAMC436-11, VMCC030-06) due to discoloration from resterilization. No immediate safety risk but may affect medical use.
AVID Medical recalls ROBOTIC URO/GYN PACK kits with discoloration from resterilization. Affected kits have specific model numbers and lot codes. Consumers should check their kits for discoloration and contact AVID Medical for details.
AVID Medical recalls LAPAROSCOPIC TRAY kits with model BJAC006-27 that may discolor due to resterilization. Affected kits include specific lot numbers. No action needed per recall.
AVID Medical recalls LAPAROSCOPIC GYN. Medical convenience kits with discoloration due to resterilization. Affected kits may have cosmetic issues but no safety risk.
AVID Medical recalls robotic partial nephrectomy kits with discoloration from resterilization. Affected kits have specific model and lot numbers. Consumers should contact for details.
AVID Medical recalls DAVINCI TRUCUSTOM BUNDLE kits with discoloration due to resterilization. Affected models include MAMC228-13 to MAMC228-15. No action needed as discoloration is cosmetic.
AVID Medical recalls medical convenience kits for laparoscopic prostatectomy due to discoloration from resterilization. Affected kits may have visual issues during surgery.
AVID Medical recalls LAVH Pack medical kits with discoloration due to resterilization. Affected kits have specific model numbers and lot numbers. Consumers should check their kit details to determine if recalled.
AVID Medical recalls Pack General Robotic medical kits due to discoloration from resterilization. Affected kits have specific model numbers and lot codes. No action needed for safety.
