Date Initiated by Firm | July 12, 2022 |
Create Date | August 31, 2022 |
Recall Status1 |
Open3, Classified |
Recall Number | Z-1667-2022 |
Recall Event ID |
90662 |
510(K)Number | K142761 |
Product Classification |
Prosthesis, hip, semi-constrained, metal/polymer, cemented - Product Code JDI
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Product | TaperFit Stem, Size 0, 38mm OFFSET, 12/14 Taper + 188.550 Centraliser, For Cemented Use, REF 588.3800. Orthopedic hip implant component. |
Code Information |
Model #588.3800, Lot #494754; UDI 05055343871065 |
Recalling Firm/ Manufacturer |
Corin Ltd Unit 1-57-8 Corinium Centre Cirencester United Kingdom
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For Additional Information Contact | Mr. Dardan Uka 441285659866 |
Manufacturer Reason for Recall | Some of the devices did not pass fatigue testing. |
FDA Determined Cause 2 | Under Investigation by firm |
Action | The recalling firm issued the recall letter dated 7/8/2022 via email to the consignee on 7/12/2022. The recall letter described the potential issue and listed the affected product. The potential risk was reported and the actions to be carried out by the customer, which included return of the product from the field and completion of the acknowledgement form to be returned via email to confirm receipt of the letter. |
Quantity in Commerce | 1 |
Distribution | Distribution was made to NJ. There was no military/government distribution. |
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 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
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510(K) Database | 510(K)s with Product Code = JDI
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