FDA Recall Terminated

Smiths Medical, BCI Advisor Vital Signs Monitor, Product Reorder No 92M774325A.

Recall: Z-1692-2015 · Initiated March 21, 2015

Recall

Recall Number
Z-1692-2015
Event Number
70793
Firm
Smiths Medical ASD, Inc.
FEI Number
2183502
Product Code
CCK
Status
Terminated
Root Cause
Nonconforming Material/Component
Initiated
March 21, 2015
Posted
May 29, 2015
Terminated
November 20, 2015
Address
1265 Grey Fox Rd, Saint Paul, MN, 55112-6929

Description

Smiths Medical, BCI Advisor Vital Signs Monitor, Product Reorder No 92M774325A.

Reason

The Auxiliary Serial Input/ Output Modes on the Advisor do not function as expected, resulting in data formatting issues or incorrect data being transmitted in or out of the serial port into a data collection system.

Action

Consignee was sent on 3/20/2015 a Smiths Medical "Urgent Medical Device Recall" letter dated 13 March 2015. The letter was addressed to Supplier Quality. The letter described the issue and the product affected by the recall. Requested consignees to quarantine the affected product and to complete and return the Confirmation Form by Fax to 1-800-237-8033 or by email to [email protected] within 10 days of receipt of this letter. Customers shall report any issues with these products to Smiths Medical's Global Complaint Department at 1-866-216-8806 or [email protected]. For questions they can contact Smiths Medical's Customer Service Department at 1-800-258-5361. UPDATE 4-20-2015 Smiths Medical sent an Urgent Medical Device Recall letter via email to the one consignee on April 10, 2015. The letter identified the additional monitors and requested that those devices be quarantined, return the attached confirmation form, and a customer service representative will contact the consignee to arrange for exchange of the affected Advisor monitors for credit or replacement.

Distribution

MN

Quantity

5 UPDATE 4-20-2015 to include 10 additional devices