Critical Alert
AVID Medical Recalls Halyard CARDIAC CATH PACK SAN23CARDQ kit
This is a Class I recall — the most serious type. There is a reasonable probability of serious health consequences or death.
Source: FDA
CriticalRecall #Z-1971-2026Medical Device
AVID Medical Recalls Halyard CARDIAC CATH PACK SAN23CARDQ kit
AVID Medical, Inc. · Class I — Most Serious
Product Description
Halyard CARDIAC CATH PACK SAN23CARDQ kit. Model Number: DRCC36.
Reason for Recall
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.
FDA Classification
Class I — Most Serious
A situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Distribution
US distribution to FL, IL, MO, MS, NC, NE, TX.
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
411 Press Analysis
AVID Medical, Inc. is recalling a medical device classified as Class I by the FDA — the highest risk level. The recall was initiated on March 13, 2026 affecting 180 kits. 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. It was distributed nationwide. Consumers and healthcare professionals should exercise caution and discontinue use of the recalled product. Contact the recalling firm directly for return or disposal instructions.
Sources: FDA openFDA Enforcement Database
This recall appears in: Medical Device Defects.