Bactiseal Endoscopic Ventricular Catheter: EVC- Catheter is designed for use in the treatment of hydrocephalus when shunting cerebrospinal fluid (CSF) from the ventricles of the brain. Part Number: 823087
FDA Recall Z-0725-2021 · Posted None
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Recalling FirmIntegra LifeSciences Corp.
Recall StatusTerminated
Product CodeJXG
Date Initiated2020-12-14
Date Terminated2021-07-19
Product Quantity17 units
Reason for Recall
Mislabeled product-Bactiseal Ventricular Catheter with Bactiseal Shunt System(823073) mislabeled as Bactiseal Endoscopic Ventricular Catheter (823087) and vs. versa
Firm Action
Integra Lifesciences notified consignees (Hospitals and Sales Representatives ) by Urgent Medical Device Recall letter between December 14 and 16, 2020 via courier service, facsimile or email about the initial notification between December 14 and 16, 2020. Letter state reason for recall, health risk and action to take:
Customers
a. If you do have the affected product in Table 1, remove the product from service.
b. Complete the attached acknowledgement form. If you do have affected product, check the box I do
have affected product. Record the total quantity of the affected product you have.
c. If you do not have affected product, check the box, I do not have affected product.
d. Return the completed acknowledgement form to [email protected]
or FAX to 1-609-750-4220
e. Keep a copy of the form for your records.
f. When your form is received, and it is noted that you have the affected product, Customer Service will contact you and provide a Return Material Authorization (RMA) number and directions to return the product. A replacement order will also be placed for the quantity noted on the form.
Questions regarding these instructions, please contact Customer Service:
USA: 800-654-2873
Monday- Friday 8:00AM EST 6:00PM EST
[email protected]
Root Cause
Labeling Change Control
Distribution Pattern
US Nationwide distribution.
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.
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