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U.S. Department of Health and Human Services

Class 2 Device Recall SEGMENTAL STEM

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 Class 2 Device Recall SEGMENTAL STEMsee related information
Date Initiated by FirmSeptember 01, 2023
Date PostedMay 29, 2025
Recall Status1 Open3, Classified
Recall NumberZ-1883-2025
Recall Event ID 96782
510(K)NumberK203815 
Product Classification Prosthesis, hip, semi-constrained, metal/polymer, cemented - Product Code JDI
ProductEthos Collar Stem, Cemented, Fluted, 100MM, 1 EACH. Model Numbers: HC-09100-03M, HC-10100-03M, HC-11120-03M, HC-13120-03M, HC-15120-03M, HC-17120-03M. Component of ELEOS SEGMENTAL LIMB SALVAGE SYSTEM
Code Information a. Model Number: HC-09100-03M; UDI-DI: 278HC0910003M0; Lot Numbers: 1880652, 1880653, 1880654, 1880655, 1880656, 1880657, 1880658, 1880659, 1880660, 1880661, 1880662, 1880663, 1880664, 1880665, 1880666, 1880667, 1880668, 1880669, 1880670, 1880671, 1880672, 1880673, 1880674, 1880675, 1880676, 1880677, 1880678, 1880679, 1880680, 1880681, 1880682, 1880683, 1880684, 1880685. b. Model Number: HC-10100-03M; UDI-DI: B278HC1010003M0; Lot Numbers: 1880686, 1880687, 1880688, 1880689, 1880690, 1880691, 1880692, 1880693, 1880694, 1880695, 1880696, 1880697, 1880698, 1880699, 1880700, 1880701, 1880702, 1880703, 1880704, 1880705, 1880706, 1880707, 1880708, 1880709, 1880710, 1880711, 1880712, 1880713, 1880714. c. Model Number: HC-11120-03M; UDI-DI: B278HC1112003M0; Lot Numbers: 1880715, 1880716, 1880717, 1880718, 1880719, 1880720, 1880721, 1880722, 1880723, 1880724, 1880725, 1880726, 1880727, 1880728, 1880729, 1880730, 1880731, 1880732, 1880733, 1880734, 1880735, 1880736, 1880737, 1880738, 1880739, 1880740, 1880741, 1880742, 1880743, 1880744, 1880745, 1880746, 1880747, 1880748, 1880749, 1880750, 1880751, 1880752, 1880753, 1880754, 1880755, 1880756, 1880757, 1880758, 1880759, 1880760, 1880761, 1880762, 1880763, 1880764, 1880765. d. Model Number: HC-13120-03M; UDI-DI: B278HC1312003M1; Lot Numbers: 1880766, 1880767, 1880768, 1880769, 1880770, 1880771, 1880772, 1880773, 1880774, 1880775, 1880776, 1880777, 1880778, 1880779, 1880780, 1880781, 1880782, 1880783, 1880784, 1880785, 1880786, 1880787, 1880788, 1880789, 1880790, 1880791, 1880792, 1880793, 1880794, 1880795, 1880796, 1880797, 1880798, 1880799, 1880800, 1880801, 1880802, 1880803, 1880804, 1880805, 1880806, 1880807, 1880808, 1880809, 1880810, 1880811. e. Model Number: HC-15120-03M; UDI-DI: B278HC1512003M0; Lot Numbers: 1880812, 1880813, 1880814, 1880815, 1880816, 1880817, 1880818, 1880819, 1880820, 1880821, 1880822, 1880823, 1880824, 1880825, 1880826, 1880827, 1880828, 1880829, 1880830, 1880831, 1880832, 1880833, 1880834, 1880835, 1880836, 1880837, 1880838, 1880839, 1880840, 1880841, 1880842, 1880843, 1880844, 1880845, 1880846, 1880847. f. Model Number: HC-17120-03M; UDI-DI: ; Lot Numbers: 1880848, 1880849, 1880850, 1880851, 1880852, 1880853, 1880854, 1880855, 1880856, 1880857, 1880858, 1880859, 1880860, 1880861, 1880862, 1880863, 1880864, 1880865, 1880866, 1880867, 1880868, 1880869, 1880870, 1880871, 1880872, 1880873, 1880874, 1880875, 1880876, 1880877, 1880878, 1880879, 1880880, 1880881, 1880882, 1880883, 1880884.
Recalling Firm/
Manufacturer		 Onkos Surgical, Inc.
77 E Halsey Rd
Parsippany NJ 07054-3714
For Additional Information ContactSean Curry
201-650-7349
Manufacturer Reason
for Recall		Potential for breach of Tyvek seals.
FDA Determined
Cause 2		Packaging change control
ActionOnkos Surgical began notifying consignees on about 09/01/2023 via email. Consignees were instructed to complete and return the response form providing the affected lot numbers being returned, coordinate the return of affected units, and to note that when placing these parts into totes, always place them flat.
Quantity in Commerce233 units
DistributionProduct was shipped from Onkos' distribution in Olive Branch, MS to consignees in the following states: GA, TX, WA, LA, NJ, FL, AZ, MD, MS, KS, IL, WI, KY, PA, NC, NE, OH, HI.
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 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
510(K) Database510(K)s with Product Code = JDI
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