Class II
Medical Device Recall: SURGIFOAM" Absorbable Gelatin Powder Kit, Product Code 1979.
Ethicon, Inc. · April 23, 2024
Reason for Recall
Some applicator tips from these lots had open seals.
Distribution
US Nationwide distribution in the states of AR, CA, FL, GA, ID, IL, IN, KY, MA, MD, MN, MO, NC, NE, NJ, PA, TN, TX, WI.
States Affected
NATIONWIDE
Quantity Affected
5,184 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1881-2024
Status: ongoing
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