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U.S. Department of Health and Human Services

Class 2 Device Recall SeaSpine Mariner RDX System

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  Class 2 Device Recall SeaSpine Mariner RDX System see related information
Date Initiated by Firm February 15, 2024
Date Posted April 22, 2024
Recall Status1 Open3, Classified
Recall Number Z-1605-2024
Recall Event ID 94164
510(K)Number K222110  
Product Classification Thoracolumbosacral pedicle screw system - Product Code NKB
Product Mariner RDX Polyaxial Head, REF: MX1-000020;
Mariner RDX Extended Polyaxial Head, REF: MX1-000030;
Mariner RDX Deformity Head, REF: MX1-000040;
Mariner RDX Extended Deformity Head, REF: MX1-000050;
Mariner RDX Trauma Head, REF: MX1-000060;
Mariner RDX Extended Trauma Head. REF: MX1-000070,
part of Mariner RDX Alpha Instruments and Implants, REF: AMRDX and
Mariner RDX TD Alpha Implants, REF: AMRDXTD, which are pedicle screw systems.
Code Information REF/UDI-DI/Lots: MX1-000020/10889981289751/AW161073C, AW164798D, AW164799D, AW164800E, AW164801E; MX1-000030/10889981289768/AW164802F, AW164803G, AW157588F, AW161074F, AW163331F; MX1-000040/10889981289775/AW157589D, AW164806E; MX1-000050/10889981289782/AW164807G, AW164808G, AW164809H, AW157590G, AW172902H; MX1-000060/10889981289799/AW157591D, AW161076E, AW164811E; MX1-000070/10889981289805/AW163350G, AW164812G, AW157592G, AW161077G; AMRDX/10889981291266/AMRDX-001, AMRDX-002, AMRDX-003, AMRDX-004, AMRDX-005, AMRDX-008, AMRDX-009; AMRDXTD/10889981295332/AMRDXTD-003, AMRDXTD-004, AMRDXTD-005
Recalling Firm/
Manufacturer		 SEASPINE ORTHOPEDICS CORPORATION
5770 Armada Dr
Carlsbad CA 92008-4608
For Additional Information Contact
760-224-0177
Manufacturer Reason
for Recall		 Screw heads, of pedicle screw systems, have thin lead-in thread that pose a risk of intraoperative cross-threading within the locking cap/screw head interface.
FDA Determined
Cause 2		 Nonconforming Material/Component
Action On 2/14/24 the firm phoned distributors and informed them of the recall issue and next steps. On 2/16/24 the firm sent a recall communication via email. Customers were asked to arrange for the return of these sets along with any additional Mariner RDX inventory using a firm provided return label. Customers with questions or concerns can contact the Associate Product Manager, at olivia.disanto@seaspine.com
Quantity in Commerce 1579 Screw Heads
Distribution US Nationwide distribution in the states of MI, GA, VA, IN, FL.
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 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
510(K) Database 510(K)s with Product Code = NKB and Original Applicant = SeaSpine Orthopedics Corporation
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