AVID Medical, Inc. recalls
65 recalls filed under AVID Medical, Inc.. The most recent was published September 9, 2026.
-
Class II · last month
AVID Medical, Inc. 1) Neuro, Acne73-01 recall: The recall notice was initiated due to a Medicom Urgent Medical Device
The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges…
-
Class II · last month
AVID Medical, Inc. Halyard medical convenience kits labeled as: 1) ENT, Model/ recall: The recall notice was initiated due to a Medicom Urgent Medical Device
The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges…
-
Class II · last month
AVID Medical, Inc. Halyard medical convenience kits labeled as: 1) A-P PACK - 205936 recall: The recall notice was initiated due to a Medicom Urgent Medical Device
The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges…
-
Class II · last month
AVID Medical, Inc. Halyard Total Joint Model/ recall: Labeling Deficiency: The medical kit labeling fails to identify
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
-
Class II · last month
AVID Medical, Inc. Halyard Total Joint Model/ recall: Labeling Deficiency: The medical kit labeling fails to identify
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
-
Class II · last month
AVID Medical, Inc. Halyard Total Joint Model/ recall: Labeling Deficiency: The medical kit labeling fails to identify
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
-
Class II · last month
AVID Medical, Inc. Halyard Total Joint Model/ recall: Labeling Deficiency: The medical kit labeling fails to identify
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
-
Class II · last month
AVID Medical, Inc. Halyard Total Joint Model/ recall: Labeling Deficiency: The medical kit labeling fails to identify
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
-
Class II · last month
AVID Medical, Inc. Brand Name: Halyard Product Name: Davinci Trucustom Bundle recall: Labeling Deficiency: The medical kit labeling fails to identify
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
-
Class II · last month
AVID Medical, Inc. Halyard Total Joint Model/ recall: Labeling Deficiency: The medical kit labeling fails to identify
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.
-
Class II · 2 months ago
AVID Medical, Inc. Halyard Lavh Pack, Model/ recall: The kit component was subjected to EO sterilization
The kit component was subjected to EO sterilization, contrary to the manufacturer recommendation, which may have led to the component leaking in a…
-
Class I · 2 months ago
AVID Medical, Inc. Halyard convenience kits containing recalled Medline Namic recall: Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds
Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufacturer due to presence of particulates…
-
Class I · 2 months ago
AVID Medical, Inc. Halyard convenience kits containing recalled Medline Namic recall: Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds
Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufacturer due to presence of particulates…
-
Class I · 2 months ago
AVID Medical, Inc. Halyard convenience kits containing recalled Medline Namic recall: Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds
Affected kits contain Medline Namic Angiographic Star Off Handle Manifolds, which were recalled by the manufacturer due to presence of particulates…
-
Class II · 3 months ago
AVID Medical, Inc. Halyard EYE PACK. Model/ recall: Incorrect concentration of Betadine solution contained within certain AVID
Incorrect concentration of Betadine solution contained within certain AVID convenience kits.
-
Class II · 3 months ago
AVID Medical, Inc. Halyard Standard Line Insertion Pack. Model/ recall: Defects in the silicone seal, which may result in "doming" of the silicone
Defects in the silicone seal, which may result in "doming" of the silicone seal due to improper sealing, potentially leading to fluid occlusion or…
-
Class II · 4 months ago
AVID Medical, Inc. Halyard, Eye Bag Pack. Kit Code: UIEB48-01 recall: Inadvertent distribution of sealed pouches that had not undergone validated
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
-
Class II · 4 months ago
AVID Medical, Inc. Halyard, Drape Pack. Kit Code: LMDP36-01 recall: Inadvertent distribution of sealed pouches that had not undergone validated
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
-
Class II · 4 months ago
AVID Medical, Inc. Halyard, Pain Pack. Kit Code: AMPK48-01 recall: Inadvertent distribution of sealed pouches that had not undergone validated
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
-
Class II · 4 months ago
AVID Medical, Inc. Halyard, Towel Six Pack. Kit Code: AMTS70-01 recall: Inadvertent distribution of sealed pouches that had not undergone validated
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
-
Class I · 6 months ago
AVID Medical, Inc. Halyard Perc Tray kit. Model Numbers: Slpc34-01, Slpc34-02 recall: Potential risk for Medline syringe rotating adaptor unwinding during use
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between…
-
Class I · 6 months ago
AVID Medical, Inc. Halyard Sammc Angiography kit. Model Numbers: Samm066-15 recall: Potential risk for Medline syringe rotating adaptor unwinding during use
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between…
-
Class I · 6 months ago
AVID Medical, Inc. Halyard Heart Cath, Self Regional kit recall: Potential risk for Medline syringe rotating adaptor unwinding during use
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between…
-
Class I · 6 months ago
AVID Medical, Inc. Halyard Neuro IR Peripheral kit recall: Potential risk for Medline syringe rotating adaptor unwinding during use
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between…
About this page
AVID Medical, Inc. appears here because a federal agency named it as the recalling firm or the brand on the label. A recall is not a judgement about everything the company sells — it covers only the lot codes and models listed in each notice.