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BD Focal Point"230V / 11 FOV (Refurbished), Catalog number: 490649. The BD Focal Point" Slide Profiler (formerly the Aut

FDA device recall Z-1640-2012 · posted 2012-05-21 · Terminated

Recall details

Recalling firm
Tripath Imaging, Inc.
Reason for recall
The cable tie mounts that adhere to the inside of the FocalPoint do not adhere as intended and can therefore become detached.
Action taken
BD Diagnostics first notified consignees by letter on October 6, 2011. BD Diagnostics also sent a letter dated February 2012, to all affected consignees. The letter identified the product, the problem, and the action to be taken by the consignee. Field Representatives were advised to inspect all cables, adhesive cable ties and connections to ensure they are secure. Inspections and repairs, if necessary, would be carried out at the next service call for each instrument, or no later than the next regularly scheduled preventative maintenance visit. For questions consignees were instructed to contact BD Diagnostics Technical Support at 1-877-822-7771 option 2 in the US, their local distributor, or their local BD office for any questions. For questions regarding this recall call 918-563-1624.
Root cause
Component change control
Status
Terminated
Product code
MKQ
Quantity affected
see line 1.
Distribution
Worldwide Distribution - USA including AZ, CT, IL, IN, FL, MN, NC, OK, OR, and TX and the countries of Australia, Belgium, Brazil, Canada, Japan and Thailand
Date initiated
2011-10-06
Date posted
2012-05-21
Date terminated
2012-12-03
Location
Burlington, NC

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