GalaSHAPE 3D; product code SH3D03, a medium size oval GalaSHAPE" 3D is indicated for use as a bioresorbable scaffold for soft tissue support and to repair, elevate and reinforce deficiencies where weakness or voids exist that require the addition of material to obtain the desired surgical outcome. This includes reinforcement of soft tissue in plastic and reconstructive surgery, and general soft tissue reconstruction. GalaSHAPE" 3D is also indicated for the repair of fascial defects that require the addition of a reinforcing or bridging material to obtain the desired surgical result.
FDA Recall Z-0948-2017 · Posted None
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Recalling FirmTepha Incorporated
Recall StatusTerminated
Product CodeOOD
Date Initiated2016-11-21
Date Terminated2017-01-05
Product Quantity29
Reason for Recall
Endotoxin values from testing of retains slightly exceeded the established specification.
Firm Action
Tepha Medical Devices sent a Voluntary Product Recall Notification letter dated November 22, 2016, to all affected customers. Beginning on 11/21/2016, all impacted customers were notified of the recall via phone or in person by Galatea Surgical, a wholly owned subsidiary of Tepha, responsible for the sales and marketing of GalaSHAPE 3D. That notification was followed up by the Tepha recall letter dated November 22, 2016, delivered by certified mail. Customers were instructed to do the following:
1) Immediately review your inventory for the affected lot number listed above.
2) If you do not have any of the affected lot in your inventory, complete the enclosed Recall
Acknowledgment Form, indicate that you have zero (O) inventory and fax the completed form back to (781) 357-1701 or email it to [email protected].
3) If you do have inventory from the affected lot, please complete the enclosed Recall Acknowledgement Form and fax back to Tepha, Inc. at (781) 357-1701 or email it to [email protected]. A Galatea representative will contact you to arrange for the product return.
If you have any questions or require assistance with the return of the recalled product, please call Galatea Surgical, at (781) 357-1752.
For questions regarding this recall call 781-357-1750.
Root Cause
Process design
Distribution Pattern
Nationwide Distribution to IN, CA, FL, MI, NV, and MT
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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