Halyard CARDIAC CATH PACK SAN23CARDQ kit. Model Number: DRCC36. recall (AVID Medical, Inc.)
Medical deviceClass IOngoing
Summary: AVID Medical, Inc. is recalling Halyard CARDIAC CATH PACK SAN23CARDQ kit. Model Number: DRCC36.. Reason: 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.
What is being recalled
Halyard CARDIAC CATH PACK SAN23CARDQ kit. Model Number: DRCC36.
Why
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.
How serious is it
Class I is the most serious level: FDA considers there is a reasonable probability that using or being exposed to this product will cause serious health problems or death.
Where it was sold
US distribution to FL, IL, MO, MS, NC, NE, TX. (states named: Florida, Illinois, Missouri, Mississippi, North Carolina, Nebraska, Texas)
How to tell if yours is affected
Model Number: DRCC36. UDI-DI (Kit Lot Numbers): 10809160469088 (1659651).
What to do
Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.
Recall facts
| Recall number | Z-1971-2026 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class I |
| Status | Ongoing |
| Recall started | March 13, 2026 |
| Reported | May 13, 2026 |
| Company | AVID Medical, Inc. |
| Company location | Toano, VA, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 180 kits |
More recalls from AVID Medical, Inc. · all medical device recalls · recalls from March 2026