FDA Recall Terminated

Stryker PCA 10 Degree Hooded Acetabular Insert ID 22mm, Part of the Howmedica PCA Total Hip System intended for use during total hip arthroplasty. The acetabular insert is used in conjunction with PCA Acetabular Shells and Femoral Heads to restore hip joint biomechanics.

Recall: Z-0281-2016 · Initiated October 15, 2015

Recall

Recall Number
Z-0281-2016
Event Number
72506
Firm
Stryker Howmedica Osteonics Corp.
FEI Number
3003070421
Product Code
JDI
Status
Terminated
Root Cause
Under Investigation by firm
Initiated
October 15, 2015
Posted
November 17, 2015
Terminated
June 8, 2017
Address
325 Corporate Dr, Mahwah, NJ, 07430-2006

Description

Stryker PCA 10 Degree Hooded Acetabular Insert ID 22mm, Part of the Howmedica PCA Total Hip System intended for use during total hip arthroplasty. The acetabular insert is used in conjunction with PCA Acetabular Shells and Femoral Heads to restore hip joint biomechanics.

Reason

Six (6) PCA 10 Degree Hooded Acetabular Insert-Duration 22 mm (ID) have been distributed in the US, although the 22 mm size was inadvertently omitted from 510(k) #K963612.

Action

Stryker sent an Urgent Medical Device Recall Notification letter dated October 15, 2015, to all affected customers. The notification instructed consignees on how to identify affected product; the related issue with the affected product; potential hazards; risk mitigations; and actions needed to be taken. Customers were instructed to quarantine the affected product. Consignees were asked to complete and return the attached Product Recall Acknowledgement Form within 5 days and either email ([email protected] or Fax (1-866-672-0627 ) the response form back. Customers with questions were instructed to call 201.831.5272.

Distribution

Distribution to Virginia only.

Quantity

1 unit