The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if product is utilized.
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Recall Number
Z-0921-2026
Classification
Class II
Status
Ongoing
Category
device
Initiated
2025-11-13
Reported
2025-12-24
Distribution
US Nationwide distribution in the states CA, CO, IL, KS, and MI.
Code Info
DYND04000, UDI-DI: 10193489191349(each), 20193489191346(case), Lot Number: 2023102590
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.