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U.S. Department of Health and Human Services

Class 2 Device Recall Bone Sonometer

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  Class 2 Device Recall Bone Sonometer see related information
Date Initiated by Firm September 03, 2019
Create Date October 10, 2019
Recall Status1 Terminated 3 on February 16, 2021
Recall Number Z-0112-2020
Recall Event ID 83811
PMA Number P970040 
Product Classification Bone sonometer - Product Code MUA
Product Achilles Insight Bone Sonometer
Code Information System ID: AWI33021, AWI33682, 0911LN0007, 091133NZM31481, 091133NZM31582, 091133NZM31875, BH1055US01, 0002860952, 0002868705, 83033603652009, 83033604564999, 0002657156, ACH+12941, ACH+12946, 084733NZM31677, 2644078, 82433040028, 82433040037, 82433070008, 82433120015, 82433080005, 82433040035, 82433040039, 82433140020, 82433290005, 82433130044, 82433130045, 82433230011, 82433140022, 82433140023, 82433140021, 82433140016, 0002556007X, CY1121US01, 828330064, 828330102, 828330049, 828330082, 83033005100157, 0002752556, 83033825104417, 83033205101815, 83033209010045, IQ1287US02, IQ1084US01, IE1016LU04, IE1063LU02, IE1106LU02, IE1106LU03, IE1153US01, IE1131US01, A6165801, A185446001, A6141901, A5945702, B5313202, A6141801, A5807032, A167409101, A6089201, A156115001, A6091501, B5481117, A5314930, B5715201, B5715202, A6143401, A6082001, B120559406, A6141601, A5997501, A5959302, C5120921, A5250606, A144165602, A6122001, A6124501, A6124502, A6110401, A147112602, A258018801, B5131818, A5968201, A130541401, A5380304, A5260003, B5767801, A130693801, A174758001, A140158101, A174051701, B5131817, A6095201, M5389201, L5389201, A5809709, A5958402, A118189801, A5806323, A5161606, A101031001, A146202101, B103443901, A5152967, A5715233, C5618310, A5715240, A5715241, A5715259, A5961502, A5725504, A5307201, N5389201, C5389202, B5495516, A119703501, A6165901, A6165902, A5811908, A5367101, A5178019, A5178029, A195945609, A5304827, A5353829, A6089301, A6089303, A6089304, A6089306, A6141701, A5483703, A5958003, A5983601, A6049301, A5977401, A258022001, A5985601, A5975602, A6096703, A5358111, A51142115, A238763702, A5990601, A6001902, A236506901, A236506902, A236506903, A236506905, A236506906, A236506907, A236506908, A258022401, A258022403, A258022404, A258022405, A258022406, A258022412, A258022416, A258022419, A258022421, A258022424, A258022428, A5715201, A5715262, A5715264, A5715267, A6032002, A6032003, A6086801, A5985201, B5381901, A5980802, A5980803, A5216510, A5141812, A176817401, A6082101, A128549801, A128549803, A128549804, A161284802, A176528801, A5217506, A5114898, A5287805, KW1111US01, LB1323US01, LB1149US02, 834334016, 834334005, 834334042, 834334068, 834374457, 834334008, 834334011, 834334012, 834334030, 834334033, 834334034, 834334047, 834334017, 834334048, 834334058, 834334060, 834334066, 834334067, 834334015, 834334018, 834334057, 834334043, 834334056, 834334059, 083433NZM31194, 083433NZM31201, 083433NZM31221, 083433NZM31223, 083433NZM31259, 083433NZM31262, 083433NZM31270, 083433NZM31275, 083433NZM31427, 083433NZM31496, 083433NZM31572, 083433NZM33053, 083433NZM33054, 083433NZM33055, 083433NZM33056, 083433NZM33057, 083433NZM33377, 083433NZM33378, MU1012US01, MU1012US02, MU1012US03, ACI31938, ACI31939, ACI31940, ACI31941, 2651516, 2738051, 085633NZM33272A, 085633NZM33349G, 085633NZM33499G, OM1068US01, 0002649897, 0002507221X, 0002508220X, 843334004, 843334008, 843334010, 843334011, 843334012, 843334013, 843334015, 843334028, 843334219, 843374239, 843334000, 843334001, 843334006, 843334026, 843334027, 084333NZM31192, 084333NZM31217, 084333NZM31245, 084333NZM31429, 084333NZM31461, 084333NZM31483, 084333NZM31860, 084333NZM31874, 084333NZM32908, 084333NZM32909, 084333NZM32910, 084333NZM32911, 084333NZM32912, 084333NZM32913, 084333NZM33062, 084333NZM33063, 084333NZM33064, 084333NZM33065, 084333NZM33066, 084333NZM33067, 084333NZM33244, 084333NZM33261, 084333NZM33262, 084333NZM33263, 084333NZM33265, 084333NZM33266, 084333NZM33269, 084333NZM33274, 084333NZM33277, 084333NZM33278, 084333NZM33279, 084333NZM33280, 084333NZM33281, 084333NZM33282, 084333NZM33284, 084333NZM33298, SA2344XR01, SA2198XR01, SA2200XR01, SA2250XR01, SA2250XR02, SA2195XR04, SA2251XR01, SA2251XR07, SA2251XR08, SA2251XR09, SA2251XR10, SA2196XR01, SA2137XR02, SA2137XR03, SA2137XR07, SA2137XR01, SA2146XR02, SA2205XR01, SA2081XR01, SA2082XR01, SA2083XR01, SA2106XR01, SA2106XR03, SA2109XR01, SA2109XR02, SA2109XR03, SA2106XR02, SA2106XR04, SA1011XR06, SA1381XR02, SA1381XR03, 847334000, 847334001, 847334053, 847334058, 847334073, 847334075, 847334076, 084733NZM31243, 084733NZM31266, 084733NZM31271, 084733NZM31462, 084733NZM31471, 084733NZM31472, 084733NZM31586, 084733NZM31863, 084733NZM31872, 084733NZM31878, 084733NZM33498, 084733NZM40110A, 847334054, 847334061, 847334071, 847334074, 83033602003711, 83033602003712, 83033602003713, 83033602003714, 83033805200659, 83033809427599, 479261BD01, 492049BD01, 612711BD01, 537615BD01, 615070BD01, 717010US02, 717010US03, 717010US07, 717010US08, 717010US09, 717010US11, 483657US01, 226529BD01, 932030BD02, 579811BD01, 853330046, 853330239, 853330180, 853330215, 853330320, 853330321, 853330322, 853330323, 853330324, 853330333, 853330334, 853330335, 853330336, 853330337, 853330338, 853330339, 853330340, 853330341, 853330342, 853330347, 853330348, 853330349, 853330350, 853330351, 853330352, 853330353, 853330354, 853330358, 853330359, 853330360, 853330376, 853330377, 853330378, 853330379, 853330380, 853330381, 853330382, 853330383, 853330384, 853330385, 853330386, 853330387, 853330388, 853330389, 853330390, 853330391, 853330392, 853330394, 853330395, 853330396, 853330397, 853330398, 853330399, 853330403, 853330404, 853330405, 0853330200B, 853330256, 853330181, 853330201, 853330064, 853330216, 853330223, 853330166, 853330192, 853330212, 853330235, 853330248, 853330240, 853330191, 853330024, 853330025, 853330035, 853330036, 853330037, 853330038, 853330040, 853330045, 853330047, 853330048, 853330069, 853330070, 853330071, 853330073, 853330075, 853330076, 853330077, 853330097, 853330107, 853330108, 853330137, 853330138, 853330139, 853330140, 853330141, 853330142, 853330143, 853330144, 853330148, 853330149, 853330150, 853330151, 853330152, 853330153, 853330167, 853330168, 853330169, 853330170, 853330171, 853330172, 853330179, 853330182, 853330183, 853330184, 853330185, 853330186, 853330187, 853330193, 853330194, 853330195, 853330196, 853330202, 853330210, 853330217, 853330218, 853330219, 0853330222D, 853330228, 853330229, 853330234, 853330236, 853330238, 853330241, 853330249, 853330250, 853330254, 853330255, 853330262, 853330263, 853330266, 853330267, 853330269, 853330270, 853330281, 853330282, 853330283, 853330284, 853330285, 853330287, 853330288, 853330290, 853330291, 853330292, 853330293, 853330294, 853330297, 853330298, 853330299, 853330300, 853330301, 853330309, 853330310, 853330311, 853330312, 856330022, 856330047, 856330075, 856330076, 856330077, 856330078, 856330079, 856330080, 856330081, 856330082, 856330093, 856330095, 856330018, 856330010, 856330011, 856330012, 856330023, 856330005, 856330021, 856330050, 856330051, 856330052, 856330053, 856330006, 856330071, 856330069, 856330056, 856330026, 856330070, 085633NZM31191, 085633NZM31203, 085633NZM31224, 085633NZM31260, 085633NZM31265, 856330055, 856330015, 856330094, 856330096, 856330001, 856330102, 856330057, AE1189XR01, AE1336XR01,  AE1145XR01, AE1148XR01, AE1165XR01, AE1241XR01, AE1223XR01, AE1223XR02, AE1154XR01, AE1201XR01, AE1221XR01, AE1223XR03, AE1223XR11, AE1224XR01, AE1237XR01, AE1149XR03, AE1243XR01, 20505RAD01, 20246RAD01, 20146RAD03, 11235RAD01, 10919RAD01 
Recalling Firm/
Manufacturer		 GE Healthcare, LLC
3000 N Grandview Blvd
Waukesha WI 53188-1615
For Additional Information Contact
800-437-1171
Manufacturer Reason
for Recall		 Certain Achilles Express and Achilles Insight systems were shipped with European CEE-7/7 Type Power Cords to countries where three protruding pin plugs are required for protective earth connection.
FDA Determined
Cause 2		 Device Design
Action GE Healthcare notified customers on about 09/03/2019, via "URGENT MEDICAL DEVICE CORRECTION" letter. Customers were informed of two (2) safety issues. The first safety issue was that certain Achilles Express and Achilles Insight systems were shipped with European CEE-7/7 Type Power Cords to countries where three protruding pin plugs are required for protective earth connection. This issue could lead to an electric shock. There have been no reported injuries as a result of this issue. Specific safety instructions included to continue using the system after following the below instructions: 1. Inspect the power cord set used on your Achilles Express or Achilles Insight system and ensure its compatibility with your wall socket; 2. Use the European CEE 7/7 Type plug only with the two wall sockets because the protective earthing connection will not be established with any other socket; 3. Do not use any adapters with your plug or wall socket; 4. If you have a CEE 7/7 Type plug and a wall socket other than that shown in Figure 2 of the letter, discontinue use of your system. Your power cord set will be replaced with the correct power cord. Destroy the incorrect power cord to ensure it is not used. The second safety issue is that certain Achilles Express and Achilles Insight systems were shipped with 125V rated power cords (type B plug) to these countries where the mains voltage could be greater than 200V. This issue could lead to an electric shock. There have been no reported injuries as a result of this issue. Specific safety instructions included, that for certain systems in Peru, Philippines and Thailand, a power cord type B plug rated at 125V, as shown in Figure 3, was shipped. The mains voltage in these countries could be greater than 200V and, as a result, this plug should not be used. If you are located in one of these three countries with mains voltage greater than 200V and have the plug shown in Figure 3 of the letter, disconnect your Achil
Quantity in Commerce 599 devices
Distribution Nationwide distribution to AZ, GA, MT, NC, NJ, NY, OH, WI. International distribution to Australia, Bahrain, Bangladesh, Brazil, Cambodia, Chile, China, Colombia, Cyprus, Hong Kong, India, Iraq, Ireland, Italy, Kuwait, Lebanon, Malaysia, Mauritius, Mexico, MEXICO, Myanmar, Nepal, Oman, Panama, Peru, Philippines, Saudi Arabia, Singapore, Sri Lanka, Switzerland, Taiwan, Thailand, United Arab Emirates, United Kingdom, Uruguay, Vietnam
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.
PMA Database PMAs with Product Code = MUA and Original Applicant = GE LUNAR CORP.
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