Medicrea Pass LP Blunt K-wire 01.6mm x 500mm-Nitinol Product reference: A06010140
FDA Recall Z-0828-2020 · Posted None
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Recalling FirmMedicrea International
Recall StatusOpen, Classified
Product CodeKWP
Date Initiated2019-09-16
Product Quantity190 units
Reason for Recall
Conical Cannulated Screws may not accept 1.6mm K-Wire, it cannot enter the minimum tolerance axis threaded
Firm Action
Medicrea International issued letter dated 9/12/19 to US Distributor stating reason for recall, health risk and action to take: Immediately check your internal inventory and quarantine all subject devices pending return to MEDICREA
2. Circulate this Field Safety Notice internally to all interested/affected parties.
3. Inform MEDICREA if any of the subject devices have been distributed to other
organisations. Please inform MEDICREA of any adverse events concerning the use of the subject devices 2. Please comply with any local laws or regulations concerning the notification of adverseevents to your National Competent Authority. 3. Complete the attached customer response form. It may be that you no longer have any physical inventory on site.
Contact: Karine TROGNEUX, MEDICREA INTERNATIONAL
Regulatory Affairs Manager, Direct : +33(0)4.69.85.95.39, Standard : +33 (0)4.72.01.87.87. Fax - N +33 (0)04 72 01 87 88, Mail : [email protected]
Root Cause
Process control
Distribution Pattern
Nationwide
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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