FDA Recall Terminated

BD Phoenix PMIC-108 Panels, Catalog number 448418, labeled in part ***Becton, Dickinson and Company 7 Loveton Circle Sparks, USA. The BD Phoenix" Automated Microbiology system is intended for the rapid identification (ID) and antimicrobial susceptibility testing (AST) of clinically significant bacteria.

Recall: Z-0570-2013 · Initiated November 6, 2012

Recall

Recall Number
Z-0570-2013
Event Number
63737
Firm
Becton Dickinson & Co. BD Diagnostic Systems
FEI Number
1119779
Product Code
LON
Status
Terminated
Root Cause
Nonconforming Material/Component
Initiated
November 6, 2012
Posted
December 19, 2012
Terminated
January 9, 2013
Address
7 Loveton Circle, Sparks, MD, 21152-0999

Description

BD Phoenix PMIC-108 Panels, Catalog number 448418, labeled in part ***Becton, Dickinson and Company 7 Loveton Circle Sparks, USA. The BD Phoenix" Automated Microbiology system is intended for the rapid identification (ID) and antimicrobial susceptibility testing (AST) of clinically significant bacteria.

Reason

An antibiotic susceptibility test kit may produce false intermediate or false resistant results with clinically significant bacteria.

Action

The firm, BD, sent an "URGENT PRODUCT RECALL" letter dated November 2012 via the telephone and fax to its customers. The letter described the product, problem and actions to be taken. The customers were instructed to immediately discontinue use and discard any remaining packages for replacement and to complete and return the Acknowledgement Receipt Form, whether or not you have any inventory remaining, via fax to: BD Regulatory Compliance at 410-316-4258. BD will issue replacements for the discarded materials. If further assistance is needed regarding replacements please contact BD Customer Service Department at 1-800-675-0908. For all other inquiries, please contact BD Technical Services Department at 1-800-638-8663.

Distribution

Nationwide distribution: USA including states of: AR, CA, KY, OK, RI, WI, and WY.

Quantity

12,250 tests