Class II
Medical Device Recall: CARDIAC ROBOT PACK. Medical convenience kit.
AVID Medical, Inc. · June 11, 2025
Reason for Recall
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
Distribution
Domestic: CA, IL, MD, OH, PA, TX, WA.
States Affected
CA, IL, MD, OH, PA, TX, WA
Quantity Affected
20 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2241-2025
Status: ongoing
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