Cook Vascular Inc. Flexipet Denuding pipette 130 micron. The product is boxed with 5 vials of 10. The device is used for the intracytoplasmic single sperm injection of oocytes. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Flexipet Denuding pipette 130 micron. The product is boxed with 5 vials of 10. The device is used for the intracytoplasmic single sperm injection of oocytes.
Brand
Cook Vascular Inc.
Lot Codes / Batch Numbers
Lot number N74091
Products Sold
Lot number N74091
Cook Vascular Inc. is recalling Flexipet Denuding pipette 130 micron. The product is boxed with 5 vials of 10. The device is used f due to mislabeled - 300 micron flexipets labeled as 130 micron and vice versa. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
mislabeled - 300 micron flexipets labeled as 130 micron and vice versa
Recommended Action
Per FDA guidance
The recalling firm issued an Urgent product Recall letter on 3/3/08. The letter informed the customers of the problem and that the pouch is correctly labeled. Customers were instructed to return product and notify any sub accounts. Please contact Cook Vascular at 1-724-845-8621 for assistance.
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 noticeDistribution
As reported by FDA
CA, FL, GA, IN, NV, NJ, NM, WA, WI
Page updated: Jan 10, 2026