Gyrus ACMI Corporation Gyrus ACMI Tripolar Ultra Cutting Forceps: 5 mm X 32 cm-Reference Number: TRU5-32 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Gyrus ACMI Tripolar Ultra Cutting Forceps: 5 mm X 32 cm-Reference Number: TRU5-32
Brand
Gyrus ACMI Corporation
Lot Codes / Batch Numbers
Lot Nos. : 6236019, 6236020, 6236021, 6258015, 6297001, 6300013, 6306015, 6320041, 6326021, 6326097, 6335042, 6342008, 6349001, 6349002, 6355029, 7011002, 7011003, 7019012
Products Sold
Lot Nos. : 6236019, 6236020, 6236021, 6258015, 6297001, 6300013, 6306015, 6320041, 6326021, 6326097, 6335042, 6342008, 6349001, 6349002, 6355029, 7011002, 7011003, 7019012
Gyrus ACMI Corporation is recalling Gyrus ACMI Tripolar Ultra Cutting Forceps: 5 mm X 32 cm-Reference Number: TRU5-32 due to Product sterility may be compromised due to failure of the tray seal packaging. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Product sterility may be compromised due to failure of the tray seal packaging
Recommended Action
Per FDA guidance
Gyrus ACMi issued recall letters on 2/19/07. Each account is asked to remove recalled product and return product .
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