510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
Z-1493-2015Class II

CROSSCHECK(R) Plating system, MTP CX Plate, Right, REF CCP-MPX1R. Orthopedic use

Wright Medical Technology Inc / initiated 2015-03-06 / Terminated / root cause: manufacturing process

Wright Medical Technology, Inc. began a recall of CROSSCHECK(R) Plating system, MTP CX Plate, Right, REF CCP-MPX1R. Orthopedic use on . FDA classified it as Class II and gives the reason as "The minor diameter, major diameter, thread pitch, and pitch on the Crosscheck are out of specification, which may result in intraoperative malfunction". As of , the recall status on record is Terminated, and MDM tags the root cause as manufacturing process.

Recall record

Recall number
Z-1493-2015
Classification
Class II
Status
Terminated
Initiated
Posted
Terminated
Recalling firm
Wright Medical Technology Inc
Product
CROSSCHECK(R) Plating system, MTP CX Plate, Right, REF CCP-MPX1R. Orthopedic use.
Product code
HRS Plate, Fixation, Bone
Reason for recall
The minor diameter, major diameter, thread pitch, and pitch on the Crosscheck are out of specification, which may result in intraoperative malfunction
Root cause tag
manufacturing process
FDA root cause
Nonconforming Material/Component
Action
Firm has initiated the recall on 03/06/2015 through written communication via Fed Ex P1 delivery to all Wright Medical Technologies distributors (hubs). Follow-up to non-responding consignees will commence 30 days after initiation. Effectiveness checks will be performed through the confirmation of returned product via a validated ERP system, a returned/signed verification form, and in the case of non-responders, a phone call, e-mail or follow up letter, depending on the region and availability of consignee.
Quantity in commerce
172 units
Distribution
Nationwide Distribution.
Product codes and lots
Lot Numbers: 35049-15A, 35049-15A-1, 35864, 358641, 362772, 36277-2-1

Enforcement reports

One row per recalled product line
FDA enforcement reports joined to recall event Z-1493-2015
Recall numberClassStatusVoluntary or mandatedReport dateClassified
Z-1482-2015Class IITerminatedVoluntary: Firm initiated
Z-1483-2015Class IITerminatedVoluntary: Firm initiated
Z-1484-2015Class IITerminatedVoluntary: Firm initiated
Z-1485-2015Class IITerminatedVoluntary: Firm initiated
Z-1486-2015Class IITerminatedVoluntary: Firm initiated
Z-1487-2015Class IITerminatedVoluntary: Firm initiated
Z-1488-2015Class IITerminatedVoluntary: Firm initiated
Z-1489-2015Class IITerminatedVoluntary: Firm initiated
Z-1490-2015Class IITerminatedVoluntary: Firm initiated
Z-1491-2015Class IITerminatedVoluntary: Firm initiated
Z-1492-2015Class IITerminatedVoluntary: Firm initiated
Z-1493-2015Class IITerminatedVoluntary: Firm initiated
Z-1494-2015Class IITerminatedVoluntary: Firm initiated
Z-1495-2015Class IITerminatedVoluntary: Firm initiated
Z-1496-2015Class IITerminatedVoluntary: Firm initiated
Z-1497-2015Class IITerminatedVoluntary: Firm initiated
Z-1498-2015Class IITerminatedVoluntary: Firm initiated
Z-1499-2015Class IITerminatedVoluntary: Firm initiated
Z-1500-2015Class IITerminatedVoluntary: Firm initiated