Z-0772-04

Codman Holter Salmon Rickham Reservoir with Ventricular Catheter Catalog Number: 82-1617

Name: Z-0772-04 Codman Holter Salmon Rickham Reservoir with Ventricular Catheter Catalog Number: 82-1617
Creator: Codman & Shurtleff, Inc.
Published: 2004-03-11
License: https://open.fda.gov/license/

Cerenovus, Inc. / initiated 2004-03-11 / Terminated

FDA source

Codman & Shurtleff, Inc. began a recall of Codman Holter Salmon Rickham Reservoir with Ventricular Catheter Catalog Number: 82-1617 on 2004-03-11. The reason FDA records is "Drainage tips absent from catheter tip". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0772-04
Status: Terminated
Initiated: 2004-03-11
Posted: 2004-07-20
Terminated: 2004-04-21
Recalling firm: Cerenovus, Inc.
Product: Codman Holter Salmon Rickham Reservoir with Ventricular Catheter Catalog Number: 82-1617
Product code: HCA Catheter, Ventricular
Reason for recall: Drainage tips absent from catheter tip
FDA root cause: Other
Action: Codman telephoned direct customers by telphone on 3/11/04. Accounts were requested to return product.
Quantity in commerce: 39 units
Distribution: CA, GA, MI, ,NC, SC, TN, TX Foreign: Italy and Germany
Product codes and lots: Lot Number: 1106525

Product code HCA

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)