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U.S. Department of Health and Human Services

Class 2 Device Recall BD Phoenix PMIC108 Panels

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 Class 2 Device Recall BD Phoenix PMIC108 Panelssee related information
Date Initiated by FirmNovember 06, 2012
Date PostedDecember 19, 2012
Recall Status1 Terminated 3 on January 09, 2013
Recall NumberZ-0570-2013
Recall Event ID 63737
510(K)NumberK070809 
Product Classification System, test, automated, antimicrobial susceptibility, short incubation - Product Code LON
ProductBD 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.
Code Information Lot number 2053373
Recalling Firm/
Manufacturer		 Becton Dickinson & Co.
BD Diagnostic Systems
7 Loveton Circle
Sparks MD 21152-0999
For Additional Information ContactMs. Gail Claiborne
410-316-4054
Manufacturer Reason
for Recall		An antibiotic susceptibility test kit may produce false intermediate or false resistant results with clinically significant bacteria.
FDA Determined
Cause 2		Nonconforming Material/Component
ActionThe 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.
Quantity in Commerce12,250 tests
DistributionNationwide distribution: USA including states of: AR, CA, KY, OK, RI, WI, and WY.
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database510(K)s with Product Code = LON
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