Recall StatusOpen, Classified
Date Initiated2022-10-14
Product Quantity95 units
Reason for Recall
Due to a defect in the outer pouch sterile seal
Firm Action
On 10/03/2022, the firm verbally notified affected customers and on 10/14/2022 sent an "URGENT: MEDICAL DEVICE CORRECTION" Letter to customer informing them that Medtronic identified a breach to the sterile barrier of the outer pouch of specific lots of VCLAS 9735560 .4MM Core Fiber 10MM Tip products.
Customer are instructed to:
immediately identify and segregate affected products within your inventory. Medtronic will contact you to facilitate product replacement when unaffected product is available.
Medtronic has determined that the inner pouches maintain sterility, accordingly, you may use segregated products ensuring the following sterile technique workflow is followed:
1. Open the affected outer pouch outside of the sterile field and remove the smaller internal pouches.
2. Per the Instruction for Use: Prior to use, examine the product packaging (in this instance the inner pouch) for damage, deterioration, and expired shelf life. If found, do not use the product.
3. Open the internal pouches using sterile technique and carefully transfer the sterile contents into the sterile field.
For questions, contact Medtronic Technical Service at 1-888-826-5603 or email at
[email protected]
Root Cause
Nonconforming Material/Component
Distribution Pattern
U.S. Nationwide distribution including in the states AZ, CA, CO, DC, FL, IL, KY, MA, MD, ME, MI, MN, MO, NH, NJ, NY, OH, PA, RI, TX, VA, WA, and WV.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.