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U.S. Department of Health and Human Services

Class 3 Device Recall hemoglobin test kits

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 Class 3 Device Recall hemoglobin test kitssee related information
Date Initiated by FirmSeptember 14, 2004
Date PostedOctober 28, 2004
Recall Status1 Terminated 3 on October 29, 2008
Recall NumberZ-0047-05
Recall Event ID 30017
510(K)NumberK840011 
Product Classification Abnormal Hemoglobin Quantitation - Product Code GKA
ProductRESOLVE Hemoglobin Test Kits packed and distributed under the Perkin Elmer Life and Analytical Sciences label, Kit Codes: FR-9120 - 120 tests per kit; FR-9400 - 360 tests per kit; and FR-9360 - 3600 tests per kit.
Code Information FR-9120 - Lot Number: 243309  FR-9360 - Lot Numbers: 213926, 213932, 213939, 213944, 220789, 220794, 220804, 220809, 220799, 220814, 220819, 220824, 220829, 220834, 220839, 220848, 220855, 220860, 220865, 220870, 220875, 220882, 220892, 220898, 228304, 228309, 228314, 228319, 228325, 228330, 228335, 228341, 228348, 228353, 228358, 228363, 228368, 228374, 228379, 228386, 228391, 228396, 229401, 228406, 234161, 234172, 234177, 234182, 234190, 234195, 234200, 234205, 234210, 234222, 234231, 234240, 234247, 234252, 234257, 234262, 238917, 234267, 234272, 234277, 238920, 238923, 238926, 238929, 238932, 238946, 238950, 238953, 238960, 238963, 242331, 242334, 242334.   FR-9400 - Lot Numbers: 213941,   220791, 220901, 220806, 220811, 220801, 220816, 220826, 220831, 220836, 220841, 220857, 220862, 220902, 220872, 220894, 220900, 228306, 228316, 228327, 228332, 228344, 228350, 228355, 228360, 228365, 228376, 228381, 228388, 228398, 228403, 228408, 2234192.    
FEI Number 1522510
Recalling Firm/
Manufacturer		 PerkinElmer LAS Inc
3985 Eastern Rd
Norton OH 44203-6215
For Additional Information ContactCindy Lloyd
330-825-4525
Manufacturer Reason
for Recall		The product insert for the test kits is incorrect with regard to the acceptable storage temperature for the Agarose IEF gel component. The kit and IEF gel labels indicate the correct storage temperature of 2-8 degrees C. The product insert incorrectly indicates that the product may be stored at 2-30 degrees C.
FDA Determined
Cause 2		Other
ActionThe firm contacted their consignees by letter dated 9/14/04.
Quantity in CommerceAll lots of test kits manufactured by the firm which have an active shelf life are subject to recall.
DistributionNationwide (The product was distributed to firms located in AR, AZ, CA, CO,FL, GA, HI, IA, IL, IN, KS, KY,LA, MA, MD, MI, MN, MO, MT, NC, NE, NJ, NM, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WI, WV )and worldwide (to 12 foreign accounts).
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 = GKA
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