TxHA PEEK IBF/TxTiHA IBF System REF BTA-151 i. TxHA The Innovasis TxHA PEEK IBF System is an intervertebral body fusion device intended to stabilize a spinal segment to promote fusion using bone graft, in order to restrict motion and decrease pain. Users of these products are limited to physicians trained in orthopedic surgery. Clinical locations include hospitals and surgery sites equipped to perform spinal surgery. ii. TxTiHA The Innovasis TxTiHA IBF System is an intervertebral body fusion device intended to stabilize a spinal segment to promote fusion using bone graft, in order to restrict motion and decrease pain.
FDA Recall Z-3163-2024 · Posted 2024-09-17
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Recalling FirmInnovasis, Inc
Recall StatusOpen, Classified
Product CodeMAX
Date Initiated2024-08-14
Product Quantity568 devices
Reason for Recall
Due to interfacing issues between the implant trial and inserter of the lumbar intervertebral fusion device.
Firm Action
On 08/14/2024, the firm sent an "URGENT: MEDICAL DEVICE RECALL" Letter via email to customers informing them of interfacing issues between the implant trial and inserter of the Tx Systems.
Customers are instructed to:
1. Please return trial sets to Innovasis for proper disposition.
2. Innovasis Distributor & Product Support (DPS) personnel will coordinate product replenishment with customers as needed.
3. Once all affected parts have been removed from inventory, a Product Removal Form will be issued to customers. This form must be filled, signed and returned for regulatory purposes. Note that this may come from an e-signature application (e.g., Adobe Sign, RightSignature, etc.).
For questions/assistance, contact DPS at 801-261-2242 or [email protected] during business hours Monday thru Friday 8:00 a.m. - 5:00 p.m. MST.
Root Cause
Device Design
Distribution Pattern
U.S. Nationwide distribution in the states of AL, CA, CO, FL, ID, MI, SD, TX and WI.
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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