ClearanceBrief
Recall Z-0689-2013 ยท

Perkinelmer

DBS MICROPLATE, TRUNCATED V-BOTTOMED Product Number: 3033-0010

DateJan 16, 2013 (initiated Nov 26, 2012)
StatusTerminated
ReasonTruncated V-Bottomed Microplate Wells used in assays contain defective wells.
Root causeProcess control
ActionPerkin Elmer initiated the recall on November 23, 2012. The Recall Letter will be delivered to the end customer by email facilitated through our PerkinElmer Technical Support group located in Akron Ohio. Technical Support will be asked to make sure the customers receive the Recall Letter and implement the recommended precautions: - Inspect the wells of row A and row H of the affected microplate lots for possible holes and cracks prior to use. - If a hole or crack is visually detected in a well of the microplate, the well should not be used for testing. - If a hole or crack is not visually d
Quantity56 kits (100 plates/kit)
DistributionNationwide Distribution.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K071649NEONATAL TOTAL GALACTOSE KIT; NEONTAL TOTAL GALACTOSE KIT, MODELS 3029-0010 AND 3029-110B
Wallac OY, Aug 7, 2008