FDA Recall Terminated

BACTEC" FX Instrument-Top, catalog #441385. The BD BACTEC" FX instrument is designed for the rapid detection of bacteria and fungi in clinical specimens. Samples are drawn from patients and injected directly into BACTEC culture vials, which are placed into the instrument for incubation and testing.

Recall: Z-2627-2011 · Initiated August 10, 2010

Recall

Recall Number
Z-2627-2011
Event Number
58873
Firm
Becton Dickinson & Co. BD Diagnostic Systems
FEI Number
1119779
Product Code
MDB
Status
Terminated
Root Cause
Software design
Initiated
August 10, 2010
Posted
June 23, 2011
Terminated
July 5, 2011
Address
7 Loveton Circle, Sparks, MD, 21152-0999

Description

BACTEC" FX Instrument-Top, catalog #441385. The BD BACTEC" FX instrument is designed for the rapid detection of bacteria and fungi in clinical specimens. Samples are drawn from patients and injected directly into BACTEC culture vials, which are placed into the instrument for incubation and testing.

Reason

In vitro diagnostic instrumentation may exhibit random operational errors that could delay effective patient treatment.

Action

BD Diagnostics Systems sent an "URGENT PRODUCT RECALL" letter dated August 2010 to all affected customers. The letter describes the product, problem and action to be taken. The letter described the type of error messages the customers may experience. All affected units will be scheduled for on site software update as well as a disk drive replacement. A BD field service engineer will contact the customers to schedule the on site visit. Customers experiencing issues prior to the scheduled visit or have questions should contact the BD Diagnostics Service Department at 800-638-8663.

Distribution

Worldwide Distribution--USA (nationwide) including countries of Australia, Belgium, Canada, China, Colombia, New Zealand, Hong Kong, Japan, Korea, Philippines, Singapore, Taiwan, and Thailand.

Quantity

907units