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.
Recall
- Recall Number
- Z-3163-2024
- Event Number
- 95185
- Firm
- Innovasis, Inc
- FEI Number
- 3004719693
- Product Code
- MAX
- Status
- Open, Classified
- Root Cause
- Device Design
- Initiated
- August 14, 2024
- Posted
- September 17, 2024
- Address
- 614 E 3900 S, Salt Lake City, UT, 84107-1902
Description
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.
Due to interfacing issues between the implant trial and inserter of the lumbar intervertebral fusion device.
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.
U.S. Nationwide distribution in the states of AL, CA, CO, FL, ID, MI, SD, TX and WI.
568 devices