Codman & Shurtleff, Inc. Codman External Drainage System 3 CSF (EDS 3) With Ventricular Catheter Catalog Numer: 82-1730 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Codman External Drainage System 3 CSF (EDS 3) With Ventricular Catheter Catalog Numer: 82-1730
Brand
Codman & Shurtleff, Inc.
Lot Codes / Batch Numbers
Lot Number: CGHBKY
Products Sold
Lot Number: CGHBKY
Codman & Shurtleff, Inc. is recalling Codman External Drainage System 3 CSF (EDS 3) With Ventricular Catheter Catalog Numer: 82-1730 due to Sterility of device is compromised due to package seal defects. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Sterility of device is compromised due to package seal defects
Recommended Action
Per FDA guidance
Codman initiated the recall on 8/04/06 by telephone with formal follow-up fax.
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