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U.S. Department of Health and Human Services

Class 2 Device Recall 2.7 Degree Angled Sagittal Saw attachment (Mako Total Knee Application Only)

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  Class 2 Device Recall 2.7 Degree Angled Sagittal Saw attachment (Mako Total Knee Application Only) see related information
Date Initiated by Firm April 25, 2019
Create Date June 16, 2019
Recall Status1 Terminated 3 on April 22, 2021
Recall Number Z-1823-2019
Recall Event ID 82738
510(K)Number K143752  
Product Classification Orthopedic stereotaxic instrument - Product Code OLO
Product 2.7 Degree Angled Sagittal Saw attachment (Mako Total Knee Application Only)
Code Information Catalog Number: 212480  Lot Number: 35040918 UDI: (01)00848486032128(10)35040918 
Recalling Firm/
Mako Surgical Corporation
2555 Davie Rd Ste 110
Davie FL 33317-7424
For Additional Information Contact Ms. Loriann Russo
Manufacturer Reason
for Recall
The bearings of the saw attachments were ungreased.
FDA Determined
Cause 2
Under Investigation by firm
Action On April 25, 2019, URGENT MEDICAL DEVICE RECALL letters under Stryker's letterhead were sent to their US consignees advising them of the issue, potential harm. This letter instructed their consignees to inform users of this device of the recall, requested that they complete the enclosed URGENT MEDICAL DEVICE RECALL BUSNESS REPLY FORM, and return all recalled product to Stryker. Actions to be taken by the Customer/ User: 1. Please inform users of this Urgent Medical Device Recall and forward this notice to all those individuals who need to be aware within your organization. 2. Hospitals/Branches/Agencies: Complete and sign the enclosed Urgent Medical Device Recall Business Reply Form and fax a copy to 1-877-496-5040 or email to Stryker10077@stericycle.com 3. Hospitals/Branches/Agencies: Return all affected instruments available at your location to the following address. Stryker Orthopaedics/PFA Product Returns Attn: Distribution Inventory Team 325 Corporate Drive Dock M-East Mahwah, NJ 07431 Ref. PFA 1958828
Quantity in Commerce 39
Distribution AR, CA, FL, KS, MA, MO, NC, NJ, NY, OH, OR, TN, and TX. Australia, China and Netherlands
Total Product Life Cycle TPLC 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) Database 510(K)s with Product Code = OLO and Original Applicant = MAKO SURGICAL CORP.