Recall Z-1881-2024— Ethicon, Inc.
Class II · Ongoing
Class II FDA medical device recall by Ethicon, Inc., initiated 2024-04-23. FDA's recall record names no specific 510(k) clearance for this event. Product: SURGIFOAM" Absorbable Gelatin Powder Kit, Product Code 1979.. Reason: Some applicator tips from these lots had open seals..
- Recalling firm
- Ethicon, Inc.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2024-04-23
- Firm location
- Somerville, NJ, United States
Product description
SURGIFOAM" Absorbable Gelatin Powder Kit, Product Code 1979.
Reason for recall
Some applicator tips from these lots had open seals.
Data sourced from openFDA. This site is unofficial and independent of the FDA.