Zinnanti Surgical Design LLC Bayonet Electrosurgical Pencil. P/N 9560575. The product is shipped in cases containing 100 blades/pencils. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Bayonet Electrosurgical Pencil. P/N 9560575. The product is shipped in cases containing 100 blades/pencils.
Brand
Zinnanti Surgical Design LLC
Lot Codes / Batch Numbers
Product Number 9560575-900. Lot numbers 3003-1, 111805, 182275, 182280, 182290, 182300, 182310, 182320, 182330, and 182340.
Products Sold
Product Number 9560575-900. Lot numbers 3003-1, 111805, 182275, 182280, 182290, 182300, 182310, 182320, 182330, and 182340.
Zinnanti Surgical Design LLC is recalling Bayonet Electrosurgical Pencil. P/N 9560575. The product is shipped in cases containing 100 blades/p due to Bubble Leak Test Failure of sterility barrier, therefore sterility of the device may be compromised. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Bubble Leak Test Failure of sterility barrier, therefore sterility of the device may be compromised
Recommended Action
Per FDA guidance
The recalling firm issued an Urgent Medical Device Recall Letter dated 7/24/07 to its single wholesaler requesting recall and sub-recall to all their consignees.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026