Class 2 Device Recall IVEA

• Date Initiated by Firm: August 24, 2017
• Date Posted: September 07, 2017
• Recall Status: Terminated on November 01, 2019
• Recall Number: Z-3239-2017
• Recall Event ID: 78019
• Product Classification: Stand, infusion - Product Code FOX
• Product: IVEA Product Part Number 16100 Model 500A
• Code Information: Serial Numbers - 100201, 100251, 100297, 100343, 100390, 100438, 100487, 100666, 100586, 100202, 100252, 100298, 100344, 100391, 100439, 100488, 100667, 100587, 100204, 100253, 100299, 100345, 100392, 100440, 100489, 100507, 100588, 100205, 100254, 100300, 100346, 100393, 100441, 100490, 100508, 100592, 100206, 100255, 100301, 100347, 100394, 100442, 100491, 100509, 100593, 100207, 100256, 100302, 100348, 100395, 100443, 100492, 100510, 100594, 100208, 100257, 100303, 100349, 100396, 100444, 100493, 100511, 100597, 100209, 100258, 100304, 100350, 100397, 100445, 100615, 100512, 100598, 100210, 100259, 100305, 100351, 100398, 100446, 100616, 100513, 100599, 100211, 100260, 100306, 100352, 100399, 100447, 100617, 100515, 100600, 100212, 100261, 100307, 100353, 100401, 100448, 100618, 100516, 100601, 100213, 100262, 100308, 100354, 100402, 100449, 100620, 100520, 100602, 100214, 100263, 100309, 100356, 100403, 100450, 100623, 100522, 100605, 100215, 100264, 100310, 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100292, 100338, 100385, 100433, 100482, 100473, 100576, 100537, 100246, 100293, 100339, 100386, 100434, 100483, 100662, 100579, 100539, 100247, 100294, 100340, 100387, 100435, 100484, 100663, 100581, 100540, 100249, 100295, 100341, 100388, 100436, 100485, 100664, 100583, 100541, 100250, 100296, 100342, 100389, 100437, 100486, 100665, 100584, 100542, 100555, 100689, 100736, 100784, 100831, 100878, 100926, 100973, 101021, 100557, 100690, 100737, 100785, 100832, 100879, 100927, 100974, 101022, 100559, 100691, 100738, 100786, 100833, 100880, 100928, 100975, 101023, 100560, 100692, 100739, 100787, 100834, 100881, 100929, 100976, 101024, 100561, 100693, 100740, 100788, 100835, 100882, 100930, 100977, 101025, 100563, 100694, 100741, 100789, 100836, 100883, 100931, 100978, 101026, 100566, 100695, 100742, 100790, 100837, 100884, 100932, 100979, 101027, 100567, 100696, 100743, 100791, 100838, 100885, 100933, 100980, 101028, 100573, 100697, 100744, 100792, 100839, 100886, 100934, 100982, 101029, 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101052, 100612, 100712, 100759, 100807, 100854, 100901, 100949, 100997, 101053, 100613, 100713, 100760, 100808, 100855, 100902, 100950, 100998, 101054, 100628, 100714, 100761, 100809, 100856, 100903, 100951, 100999, 101055, 100629, 100715, 100762, 100810, 100857, 100904, 100952, 101000, 101056, 100630, 100716, 100763, 100811, 100858, 100905, 100953, 101001, 101057, 100631, 100717, 100764, 100812, 100859, 100906, 100954, 101002, 101058, 100633, 100718, 100765, 100813, 100860, 100907, 100955, 101003, 101059, 100634, 100719, 100766, 100814, 100861, 100908, 100956, 101004, 101060, 100635, 100720, 100767, 100815, 100862, 100910, 100957, 101008, 101061, 100638, 100721, 100768, 100816, 100863, 100911, 100958, 101009, 101062, 100668, 100722, 100769, 100817, 100864, 100912, 100959, 101010, 101063, 100669, 100723, 100770, 100818, 100865, 100913, 100960, 101011, 101064, 100670, 100724, 100771, 100819, 100866, 100914, 100961, 101012, 101065, 100671, 100725, 100772, 100820, 100867, 100915, 100962, 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• Recalling Firm/ Manufacturer: Firefly Medical, Inc.; 320 E Vine Dr Ste 312; Fort Collins CO 80524-2332
• For Additional Information Contact: Firefly Medical Representative; 970-472-5323
• Manufacturer Reason for Recall: The dowel pins (P/N 16082) that fit in the left and right leg pivot castings (P/Ns 16049/16056) can rotate and gradually maneuver out of the leg casting after several hundred deployment and folding cycles (designed for easy storage) of the IVEA unit.
• FDA Determined Cause: Device Design
• Action: The recall notification is expected to begin on or before 9/8/17 after pin cap components are received for the corrections. Instructions in the recall notification letter do not include return of recall product. They are to be corrected in the field. If any units are returned, they will be labeled and quarantined until corrected by Firefly Medical personnel or the sub-contracted manufacturer supplier. The recall notification letter will be sent certified letter with return receipt.
• Quantity in Commerce: 570 units
• Distribution: United States, Australia, Belgium, Canada, China, Germany, Hong Kong, Indonesia, Israel, Netherlands, Singapore, UAE
• Total Product Life Cycle: TPLC 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.