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U.S. Department of Health and Human Services

Class 2 Device Recall ExploR 7x26mm Modular Radial Stem

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 Class 2 Device Recall ExploR 7x26mm Modular Radial Stemsee related information
Date Initiated by FirmApril 22, 2014
Date PostedMay 13, 2014
Recall Status1 Terminated 3 on January 13, 2015
Recall NumberZ-1615-2014
Recall Event ID 68144
510(K)NumberK040611 K051385 
Product Classification Prosthesis, elbow, hemi-, radial, polymer - Product Code KWI
ProductExploR 7x26mm Modular Radial Stem, Catalog number 11-210062. Elbow prosthesis orthopedic implant.
Code Information Catalog Number: 11-210062 Lot Number Identification: 972230
FEI Number 1825034
Recalling Firm/
Manufacturer		 Biomet, Inc.
56 E Bell Dr
Warsaw IN 46582-6989
For Additional Information ContactCraig Buchman
574-267-6639 Ext. 1676
Manufacturer Reason
for Recall		This lot of the ExploR Modular Radial Stem may be missing the wedge ramp threads. If the wedge ramp threads are missing from the stem, the likelihood of the set screw loosening from the radial stem intraoperatively is increased. If the set screw loosens, a revision surgery may be necessary.
FDA Determined
Cause 2		Process control
ActionBiomet sent an URGENT MEDICAL DEVICE SAFETY ALERT dated April 22, 2014 to affected customers. The letter identified the affected product, problem and actions to be taken. Questions related to this notice should be directed to (574) 372-1570, Monday through Friday, 8 a.m. to 5 p.m.
Quantity in Commerce8 devices
DistributionUS Nationwide Distribution in the states of NY, MD, NC, SC, MI, OR, and NV.
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 = KWI
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