AVID Medical Recalls
172 recalls on record · August 24, 2016 to August 12, 2026 · Medical Devices
Recalls by year
16
17
18
20
21
24
25
26
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
November 20, 2024Medical DevicesFDA
AVID Medical, Inc. recalls Halyard KIT, CARDIAC ROBOTIC - Medical convenience kits Model Number: ESJH017-03
Hazard: 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 possible foreign body reactions
November 20, 2024Medical DevicesFDA
AVID Medical, Inc. recalls Halyard KIT, SHOULDER - Medical convenience kits Model Number: ESJH014-06
Hazard: 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 possible foreign body reactions
November 20, 2024Medical DevicesFDA
AVID Medical, Inc. recalls Halyard KIT, TOTAL KNEE - Medical convenience kits Model Number: ESJH012-07
Hazard: 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 possible foreign body reactions
November 20, 2024Medical DevicesFDA
AVID Medical, Inc. recalls Halyard GENERAL SET UP PACK - Medical convenience kits Model Number: ESJH005-02
Hazard: 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 possible foreign body reactions
November 20, 2024Medical DevicesFDA
AVID Medical, Inc. recalls Halyard AORTA PACK - Medical convenience kits Model Number: ESJH004-02
Hazard: 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 possible foreign body reactions
November 20, 2024Medical DevicesFDA
AVID Medical, Inc. recalls Halyard OPEN HEART PACK MAIN - Medical convenience kits Model Number: ESJH003-02
Hazard: 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 possible foreign body reactions
November 20, 2024Medical DevicesFDA
AVID Medical, Inc. recalls Halyard ENT T AND A PACK - Medical convenience kits Model Number: EAMC106-02
Hazard: 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 possible foreign body reactions
November 20, 2024Medical DevicesFDA
AVID Medical, Inc. recalls Halyard D & C PACK-CKC - Medical convenience kits Model Number: BMGT003-02
Hazard: 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 possible foreign body reactions
November 20, 2024Medical DevicesFDA
AVID Medical, Inc. recalls Halyard IR BIOPSY PACK - Medical convenience kits Model Number: AVMD019-01
Hazard: 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 possible foreign body reactions
November 20, 2024Medical DevicesFDA
AVID Medical, Inc. recalls Halyard IR ABCESS DRAINAGE PACK - Medical convenience kits Model Number: AVMD018
Hazard: 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 possible foreign body reactions
June 16, 2021Medical DevicesFDA
Avid Medical, Inc. recalls DIALYSIS ACCESS Medical convenience kit, Avid Medical Part Number: VMED004-03.
Hazard: Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator. Under certain circumstances the applicator may grow Aspergillus penicillioides, which may result in a breach of the package integrity. A breach of package integrity may contaminate other components in AVID Medical kits.
June 16, 2021Medical DevicesFDA
Avid Medical, Inc. recalls FISTULA (ON/OFF) ALL IN ONE BAG. Medical convenience kit, Avid Medical Part Number: VAMK024-03
Hazard: Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator. Under certain circumstances the applicator may grow Aspergillus penicillioides, which may result in a breach of the package integrity. A breach of package integrity may contaminate other components in AVID Medical kits.
June 16, 2021Medical DevicesFDA
Avid Medical, Inc. recalls FISTULA ON-OFF KIT. Medical convenience kit, Avid Medical Part Number: MMTN020.
Hazard: Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator. Under certain circumstances the applicator may grow Aspergillus penicillioides, which may result in a breach of the package integrity. A breach of package integrity may contaminate other components in AVID Medical kits.
June 16, 2021Medical DevicesFDA
Avid Medical, Inc. recalls ADULT CHEST TUBE TRAY. Medical convenience kit, Avid Medical Part Number: LAKC001-04
Hazard: Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator. Under certain circumstances the applicator may grow Aspergillus penicillioides, which may result in a breach of the package integrity. A breach of package integrity may contaminate other components in AVID Medical kits.
March 25, 2020Medical DevicesFDA
Avid Medical, Inc. recalls Custom procedure trays containing medical components needed to facilitate patient procedures and to perform minor and ma
Hazard: The medical procedure trays contain one or more recalled surgical gowns. The gowns were manufactured at locations that did not maintain proper environmental conditions. There is no assurance that the surgical gowns are sterile. An inadequately sterilized surgical gown could compromise a sterile field and increase the risk of a surgical site infection. Due to the configuration of the trays, the recalled gowns may come into contact with other components within the tray posing a risk of cross contamination.
March 25, 2020Medical DevicesFDA
Avid Medical, Inc. recalls Custom procedure trays containing medical components needed to facilitate patient procedures and to perform minor and ma
Hazard: The medical procedure trays contain one or more recalled surgical gowns. The gowns were manufactured at locations that did not maintain proper environmental conditions. There is no assurance that the surgical gowns are sterile. An inadequately sterilized surgical gown could compromise a sterile field and increase the risk of a surgical site infection. Due to the configuration of the trays, the recalled gowns may come into contact with other components within the tray posing a risk of cross contamination.
March 25, 2020Medical DevicesFDA
Avid Medical, Inc. recalls Custom procedure trays containing medical components needed to facilitate patient procedures and to perform minor and ma
Hazard: The medical procedure trays contain one or more recalled surgical gowns. The gowns were manufactured at locations that did not maintain proper environmental conditions. There is no assurance that the surgical gowns are sterile. An inadequately sterilized surgical gown could compromise a sterile field and increase the risk of a surgical site infection. Due to the configuration of the trays, the recalled gowns may come into contact with other components within the tray posing a risk of cross contamination.
March 25, 2020Medical DevicesFDA
Avid Medical, Inc. recalls Custom procedure trays containing medical components needed to facilitate patient procedures and to perform minor and ma
Hazard: The medical procedure trays contain one or more recalled surgical gowns. The gowns were manufactured at locations that did not maintain proper environmental conditions. There is no assurance that the surgical gowns are sterile. An inadequately sterilized surgical gown could compromise a sterile field and increase the risk of a surgical site infection. Due to the configuration of the trays, the recalled gowns may come into contact with other components within the tray posing a risk of cross contamination.
March 25, 2020Medical DevicesFDA
Avid Medical, Inc. recalls Custom procedure trays containing medical components needed to facilitate patient procedures and to perform minor and ma
Hazard: The medical procedure trays contain one or more recalled surgical gowns. The gowns were manufactured at locations that did not maintain proper environmental conditions. There is no assurance that the surgical gowns are sterile. An inadequately sterilized surgical gown could compromise a sterile field and increase the risk of a surgical site infection. Due to the configuration of the trays, the recalled gowns may come into contact with other components within the tray posing a risk of cross contamination.
March 25, 2020Medical DevicesFDA
Avid Medical, Inc. recalls Custom procedure trays containing medical components needed to facilitate patient procedures and to perform minor and ma
Hazard: The medical procedure trays contain one or more recalled surgical gowns. The gowns were manufactured at locations that did not maintain proper environmental conditions. There is no assurance that the surgical gowns are sterile. An inadequately sterilized surgical gown could compromise a sterile field and increase the risk of a surgical site infection. Due to the configuration of the trays, the recalled gowns may come into contact with other components within the tray posing a risk of cross contamination.
March 25, 2020Medical DevicesFDA
Avid Medical, Inc. recalls Custom procedure trays containing medical components needed to facilitate patient procedures and to perform minor and ma
Hazard: The medical procedure trays contain one or more recalled surgical gowns. The gowns were manufactured at locations that did not maintain proper environmental conditions. There is no assurance that the surgical gowns are sterile. An inadequately sterilized surgical gown could compromise a sterile field and increase the risk of a surgical site infection. Due to the configuration of the trays, the recalled gowns may come into contact with other components within the tray posing a risk of cross contamination.
March 25, 2020Medical DevicesFDA
Avid Medical, Inc. recalls Custom procedure trays containing medical components needed to facilitate patient procedures and to perform minor and ma
Hazard: The medical procedure trays contain one or more recalled surgical gowns. The gowns were manufactured at locations that did not maintain proper environmental conditions. There is no assurance that the surgical gowns are sterile. An inadequately sterilized surgical gown could compromise a sterile field and increase the risk of a surgical site infection. Due to the configuration of the trays, the recalled gowns may come into contact with other components within the tray posing a risk of cross contamination.
March 25, 2020Medical DevicesFDA
Avid Medical, Inc. recalls Custom procedure trays containing medical components needed to facilitate patient procedures and to perform minor and ma
Hazard: The medical procedure trays contain one or more recalled surgical gowns. The gowns were manufactured at locations that did not maintain proper environmental conditions. There is no assurance that the surgical gowns are sterile. An inadequately sterilized surgical gown could compromise a sterile field and increase the risk of a surgical site infection. Due to the configuration of the trays, the recalled gowns may come into contact with other components within the tray posing a risk of cross contamination.
March 7, 2018Medical DevicesFDA
Avid Medical, Inc. recalls AVID TruCustom UPPER EXTREMITY convenience kits, Item Code: LGHM050-03 and LGHM050-04
Hazard: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.
March 7, 2018Medical DevicesFDA
Avid Medical, Inc. recalls AVID TruCustom SPINE convenience kits, Item Code: LITT016-04
Hazard: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.
March 7, 2018Medical DevicesFDA
Avid Medical, Inc. recalls AVID TruCustom SHOULDER ARTHROSCOPY convenience kits, Item Code: MADN010-02
Hazard: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.
March 7, 2018Medical DevicesFDA
Avid Medical, Inc. recalls AVID TruCustom PV MINOR PACK convenience kits, Item Code: MADN017-02 and MADN017-03
Hazard: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.
March 7, 2018Medical DevicesFDA
Avid Medical, Inc. recalls AVID TruCustom PLASTIC BASIN PACK convenience kits, Item Code: MADN008-03
Hazard: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.
March 7, 2018Medical DevicesFDA
Avid Medical, Inc. recalls AVID TruCustom PACEMAKER PACK (CARDIOLOGY) convenience kits, Item Code: VAMK016
Hazard: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.
March 7, 2018Medical DevicesFDA
Avid Medical, Inc. recalls AVID TruCustom PACEMAKER PACK convenience kits, Item Code: LGHM030-06
Hazard: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non Sterile Bulk needles that may contain loose polypropylene foreign material above the release specification.