Atlas FDA

BD Probetec" ET CT/GC Endocervical Specimen Collection and Dry Transport System-Pink Cap, Catalog number 440476, packed

FDA device recall Z-0969-2010 · posted 2010-03-03 · Terminated

Recall details

Recalling firm
Becton Dickinson & Co.
Reason for recall
Product was shipped beyond its expiration date.
Action taken
The recalling firm notified end users by letter flagged as "Urgent Product Recall" on 09/18/09. The notification advised that the referenced lot number had been correctly labeled with expiration date but had been shipped after the labeled date. End users were instructed to discontinue use discard product for replacement and return enclosed response form. If further assistance is needed regarding replacements, please contact SD Customer Service Department at 1-800-675-0908. For all other inquiries, please contact SD Technical Services Department at 1-800-638-8663.
Root cause
Employee error
Status
Terminated
Product code
MKZ
Quantity affected
242 packs
Distribution
The product was sold for distribution to clinical laboratories nationwide and to the firm's international affiliate in Australia.
Date initiated
2009-09-18
Date posted
2010-03-03
Date terminated
2010-03-24
Location
Sparks, MD

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