Manufacturer
115 recalls in our database name AVID Medical, Inc. as the manufacturing or recalling firm.
The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.
Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.
AVID Medical is recalling the Halyard HEART CATH SELF REGIONAL kit (Model SELF131-05) because the Medline syringe rotating adaptor may unwind during use, causing a loose or full disconnection between the syringe and manifold.
AVID Medical is recalling the Halyard CATH LAB kit (Model SACL75AM) because the syringe rotating adapter may unwind during use, causing a loose or full disconnection between the syringe and manifold.
AVID Medical is recalling Halyard CARDIAC CATH TRAY SHANDS JAX kits due to a defect in the Medline syringe rotating adaptor that may unwind during use, causing a loose or full disconnection between the syringe and manifold.
The Halyard PERC TRAY kit (models SLPC34-01 and SLPC34-02) is being recalled due to risk that a Medline syringe rotating adaptor may unwind during use, causing a loose or full disconnection between the syringe and manifold.
AVID Medical recalls Halyard Cardiac Cath Pack kits (Models EAMC1000-05, WAFB208-02) due to risk that a Medline syringe rotating adapter may unwind during use, causing loose or full disconnection between the syringe and manifold.
Halyard SAMMC ANGIOGRAPHY kits (Model SAMM066-15) are recalled because the Medline syringe rotating adapter may unwind during use, causing a loose or disconnected connection between the syringe and manifold. 2,392 kits were distributed across US states including FL, IL, MO, MS, NC, NE, and TX.
Halyard VA Detroit Cath Lab Pack kits (Model VMCD029) are being recalled due to a potential risk that the Medline syringe rotating adaptor may unwind during use, causing a loose or full disconnection between the syringe and manifold.
AVID Medical is recalling the Halyard CATH LAB kit (Model SACL75-01) due to risk that a Medline syringe rotating adaptor may unwind during use, causing loose or complete disconnection between the syringe and manifold.
AVID Medical is recalling Halyard CARDIAC CATH PACK SAN23CARDQ kits (Model DRCC36) due to a Medline syringe rotating adapter that may unwind during use, potentially causing loose or full disconnection between the syringe and manifold.
AVID Medical is recalling the Halyard NEURO IR PERIPHERAL (PS 64405) kit because the Medline syringe rotating adapter may unwind during use, causing a loose or full disconnection between the syringe and manifold.
AVID Medical is recalling Halyard Transport Bag Kits (Kit Code LIFE0080-01) due to a Tyvek bag seal defect that may compromise the sterility of the kit. No illnesses or injuries have been reported.
The Halyard organ recovery kit was recalled because the devices are unsuitable for organ transplant.
AVID Medical recalls 132 units of the Halyard ORGAN RECOVERY OR PACK (Kit Code: LLOG1000-15) due to device unsuitability for organ transplant. The recalled units were distributed nationwide in Florida, Georgia, and Puerto Rico.
AVID Medical is recalling the Halyard MINI PLUS KIT SOUTH (Kit Code JACK097-08) because the devices are not suitable for organ transplant procedures. The recall affects 380 units distributed in Florida, Georgia, and Puerto Rico.
AVID Medical is recalling the Halyard surgical pack due to potential incomplete sealing of the header bag, which may compromise sterility. The recall affects 90 units distributed to healthcare facilities in Georgia, Illinois, Nebraska, and Maryland.
AVID Medical is recalling 240 units of Halyard EP LAB Pack (Catalog ESJH009-03) due to potential incomplete seals on header bags. The affected lot was distributed to facilities in Georgia, Illinois, Nebraska, and Maryland.
AVID Medical recalls Halyard General Laparoscopy Pack due to potential incomplete seals on the header bag that could compromise product sterility.
AVID Medical is recalling 56 units of the Halyard HEAD AND NECK TRAY due to a potential for incomplete seal on the header bag, which could compromise product sterility. The recall affects units distributed in Georgia, Illinois, Nebraska, and Maryland.
AVID Medical is recalling Halyard MIDTOWN GENERAL ARTERIOGRAM devices due to potential incomplete seals on header bags that could compromise product sterility. Approximately 300 units (Lot 1635477) were distributed to healthcare facilities in Georgia, Illinois, Nebraska, and Maryland.
AVID Medical is recalling 228 Halyard CPT BASIC IR PACK convenience kits (Model 1646381) due to potential for open header bag seals that could compromise sterility. The kits were distributed in Florida.
AVID Medical is recalling Halyard ENT PACK convenience kits (Model JACK421-04) due to potential open header bag seals that could compromise product sterility. The recall affects 57 units distributed in Florida.
AVID Medical is recalling laparoscopic prostatectomy convenience kits distributed to seven states because the CLEARIFY VISUALIZATION SYSTEM component was inadvertently resterilized, causing discoloration that may affect surgical visualization.
AVID Medical is recalling 46 robotic partial nephrectomy surgery kits due to inadvertent re-sterilization of the visualization system component, which caused discoloration.
AVID Medical is recalling 574 General Laparoscopy Trays due to inadvertent resterilization causing discoloration of the CLEARIFY VISUALIZATION SYSTEM. The discoloration could compromise surgical visibility.
AVID Medical is recalling 292 LAVH Pack surgical kits due to inadvertent resterilization that caused discoloration of the CLEARIFY VISUALIZATION SYSTEM. Affected kits were distributed in seven U.S. states.