AVID Medical recalls Halyard CARDI:AC CATH PACK SAN23CARDQ kit (model DRCC36) due to potential loose connections from 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 the syringe and manifold.
AVID Medical is recalling Halyard CARDIAC CATH PACK SAN23CARDQ kits (model DRCC36) because the syringe rotating adaptor might unwind during use, causing loose connections or disconnections. This could lead to medical complications if the kit is used improperly.
The syringe rotating adaptor in the kit may unwind during use, which can cause the syringe to become disconnected from the manifold. This could lead to medical complications if the connection is not secure during procedures.
Healthcare professionals using the Halyard CARDIAC CATH PACK SAN23CARDQ kit (model DRCC36) for medical procedures are most at risk. Patients using this kit may also be affected if the connection becomes loose.
Check for the model number DRCC36 on the kit. The kit was sold with lot numbers 10809160469088 (1659651) through Medline.
Verify the model number is DRCC36 on the kit.
The recall is for potential loose connections from the syringe rotating adaptor unwinding during use, which could lead to medical complications if not addressed.
Look for the model number DRCC36 on the kit. The kit was sold with lot numbers 10809160469088 (1659651) through Medline.
The recall does not specify a remedy, so check with AVID Medical for further instructions.
We’ve drafted a message you can send AVID Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1971-2026 — AVID Medical AVID Medical Hello, I own a AVID Medical that is covered by recall Z-1971-2026 from AVID Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
