Skip to content
Recall Observatory FDA recall evidence

Device product

HVI CARDIAC ROBOT PACK. Medical convenience kit.

Z-2252-2025

June 11, 2025

Class II

Product summary

Firm
AVID Medical, Inc.
Event
Event 97149
Status
Ongoing
Classification
Class II
Quantity
20 units
Official record key
device-enforcement:Z-2252-2025

Official wording

Reason: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.

Code information: Model No. RYCB72-04; UDI: 10809160434666; Kit Lot No. 1625487.

Distribution pattern: Domestic: CA, IL, MD, OH, PA, TX, WA.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.