Date Initiated by Firm | April 10, 2015 |
Date Posted | April 29, 2015 |
Recall Status1 |
Terminated 3 on June 29, 2015 |
Recall Number | Z-1546-2015 |
Recall Event ID |
71061 |
510(K)Number | K020885 K041393 |
Product Classification |
Rod, fixation, intramedullary and accessories - Product Code HSB
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Product | Female Driver, Part number FDr101, instrument used for the insertion of the Fassier-Duval IM Telescopic System. For orthopedic procedures.
This instrument is included in the Fassier-Duval IM Telescopic System instrument tray. This instrument is marked with the catalogue number and lot number. |
Code Information |
Lot 290609-01 |
Recalling Firm/ Manufacturer |
Pega Medical Inc. 1111 Autoroute Chomedy Laval Canada
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For Additional Information Contact | Enrique Garcia 450-688-5144 |
Manufacturer Reason for Recall | The hexagonal tip of the Female Driver instrument for the Fassier-Duval IM Telescopic System is 0.06 mm under the specifications. This may result in a reduction of the total strength of the instrument, possibly leading to deformation, wear, and tip breakage. |
FDA Determined Cause 2 | Nonconforming Material/Component |
Action | The firm sent the Urgent Field Safety Notice-Recall letter, dated April 10, 2015 to consignees via email. The letter listed the affected product as FEMALE DRIVER FASSIER-DUVAL IM TELESCOPIC SYSTEM.
Consignees are requested to return devices back to the firm for disposal.
Consignees with questions should contact the firm at 450-688-5144 ext. 242 or send email to egarcia@pegamedical.com |
Quantity in Commerce | 9 units (5 units in the US and 4 units international) |
Distribution | Worldwide distribution. US in Delaware, Florida, Nebraska, and New York; Australia, Brazil, and United Kingdom. |
Total Product Life Cycle | TPLC Device Report |
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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.
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510(K) Database | 510(K)s with Product Code = HSB
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