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U.S. Department of Health and Human Services

Class 2 Device Recall DRAD, 1.8MM X 16MM, LOCKING PEG

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 Class 2 Device Recall DRAD, 1.8MM X 16MM, LOCKING PEGsee related information
Date Initiated by FirmMarch 09, 2017
Create DateApril 18, 2017
Recall Status1 Terminated 3 on August 21, 2019
Recall NumberZ-1855-2017
Recall Event ID 76729
510(K)NumberK132296 
Product Classification Screw, fixation, bone - Product Code HWC
ProductD-RAD, 1.8MM X 16MM, LOCKING PEG, QTY: (1), STERILE R, RES 74671816 Orthopedic
Code Information Batch number 15KM05493
Recalling Firm/
Manufacturer		 Smith & Nephew, Inc.
1450 E Brooks Rd
Memphis TN 38116-1804
For Additional Information ContactDavid M. Snyder
978-749-1440
Manufacturer Reason
for Recall		The expiration dates on the labeling are incorrect, the actual expiration dates are before the date on the labeling.
FDA Determined
Cause 2		Labeling Change Control
ActionSmith & Nephew sent an Urgent Medical First Recall Notice dated March 9, 2017, to all affected consignees. The letter identified the product, the problem, and the action to be taken by the consignee. The letter requested the quarantine and return of the devices, and for the distributors to notify their consignees and ensure the same actions. International consignees were notified by email. Consignees with questions were instructed to contact FieldAction@smith-nephew.com. For questions regarding this recall call 978-749-1440.
Quantity in Commerce19 units
DistributionWorldwide Distribution - US (Nationwide) Internationally to Colombia, Denmark, Finland, France, Great Britain, Italy, and Singapore
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 = HWC
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