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U.S. Department of Health and Human Services

Class 2 Device Recall REFLECTION(R), MICROSTABLE(R), ACETABULAR LINER

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 Class 2 Device Recall REFLECTION(R), MICROSTABLE(R), ACETABULAR LINERsee related information
Date Initiated by FirmNovember 25, 2013
Date PostedDecember 26, 2013
Recall Status1 Terminated 3 on February 01, 2017
Recall NumberZ-0581-2014
Recall Event ID 67042
510(K)NumberK012787 
Product Classification Prosthesis, hip, semi-constrained, metal/polymer, porous uncemented - Product Code LPH
ProductREFLECTION(R), MICROSTABLE(R), ACETABULAR LINER, 20o OVERHANG, 28 MM ID, 54-56 OD, QTY: (1), STERILE EO, REF 71742854, Smith & Nephew, Inc. Memphis, TN 38116 USA. Orthopaedic.
Code Information Batch No. 12BM04836
Recalling Firm/
Manufacturer		 Smith & Nephew Inc
1450 E. Brooks Rd
Memphis TN 38116
For Additional Information ContactJoe Metzger
978-749-1330
Manufacturer Reason
for Recall		One batch of the Reflection(TM) Polyethylene Acetabular Liners may be out of tolerance causing the liner not to fully seat into the shell.
FDA Determined
Cause 2		Other
ActionAll affected sales staff was notified of problem and the recall via email on 11/25/2013. There were no US hospitals affected by this recall.
Quantity in Commerce38 units
DistributionDistributed in China and Spain.
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 = LPH
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