MEDICREA LIGAPASS TENSION PULLEY HANDLE XS- intended to provide thoracic and/or lumbar posterior stabilization for degenerative pathologies Ref : A08200200
FDA Recall Z-0463-2021 · Posted None
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Recalling FirmMedicrea International
Recall StatusTerminated
Product CodeOWI
Date Initiated2020-10-08
Date Terminated2024-05-09
Product Quantity17 units US; 8 units OUS Expanded: 1 US and 3 OUS
Reason for Recall
Tightening the LIGAPASS Band with this instrument, the tensioner's pliers can crush the band causing the band to break during surgery and lead to a risk of infection and re-intervention ,
Firm Action
Medicrea International issued Reportable voluntary Recall notification dated 10/5/20 to via e-mail to distributors and subsidiaries stating reason for recall, health risk and action to take:
Instructions sent to US subsidiary :
1. 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.
a) Please provide contact details so that MEDICREA can inform the recipients appropriately.
b) If you are a Distributor, note that you are responsible for notifying your affected customers.
4. Please inform MEDICREA of any adverse events concerning the use of the subject devices
Please comply with any local laws or regulations concerning the notification of adverse events to your National Competent Authority.
5. Complete the attached customer response form. It may be that you no longer have any
physical inventory on site. Completing this form will allow us to update our records and will also negate the need for us to send any further unnecessary communications on this matter. Therefore please complete even if you no longer have any of the subject devices in your physical inventory.
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
Device Design
Distribution Pattern
CA Foreign:France, Belgium
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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