OsteoBallast, 45 x 17.5 mm (SeaSpine Brand), REF: 56800095. Ballast, 45 x 17.5 mm (IsoTis Brand), REF: 02-8000-095
IsoTis OrthoBiologics, Inc. · Demineralized bone matrix (DBM) in resorbable mesh indicated for use with autograft as a bone graft extender in the posterolateral spine and pelvis, were fille…
Open FDA's page for this record- Cfres ID
- 221312
- Product res number
- Z-2820-2026
- Event date initiated
- 2026-07-02
- Event date posted
- 2026-07-28
- Recall status
- Open, Classified
- Res event number
- 99332
- Product code
- MQV
- Product description
- OsteoBallast, 45 x 17.5 mm (SeaSpine Brand), REF: 56800095. Ballast, 45 x 17.5 mm (IsoTis Brand), REF: 02-8000-095
- Code info
- REF/UDI-DI/Lots: 56800095/10889981149352/181559, 181550 02-8000-095/10889981149314/181559, 181550
- Firm FEI number
- 3001503333
- Recalling firm
- IsoTis OrthoBiologics, Inc.
- Address 1
- 2 Goodyear Ste A 2 Goodyear
- Address 2
- Ste A
- City
- Irvine
- State
- CA
- Postal code
- 92618-2052
- Additional info contact
- 949-5958710
- Root cause description
- Process control
- Product quantity
- 98
- Distribution pattern
- US Nationwide distribution in the states of AK, NJ, TN, AR, CA, WA, OH.
- Reason for recall
Demineralized bone matrix (DBM) in resorbable mesh indicated for use with autograft as a bone graft extender in the posterolateral spine and pelvis, were filled with approx. 4.5 cc DBM (fill for 45 11 mm configuration) instead of approx. 7.5 cc DBM (fill for 45 17.5 mm configuration), which may lead to delayed fusion, incomplete fusion, pseudarthrosis, or lack of bone ingrowth.
- Action
On 7/2/2026, recall notices were emailed to customers informing them of the following: Orthofix does not recommend removal or revision of implanted devices containing product from the affected lots. Patients should continue to be managed according to the treating surgeon's standard clinical practice and routine follow-up schedule. Surgeons should monitor for signs or symptoms consistent with delayed fusion, incomplete fusion, pseudarthrosis, or lack of bone ingrowth and manage patients as clinically indicated. If the procedure was performed in accordance with the surgical technique and the intended intraoperative objectives were achieved, no additional patient management beyond routine postoperative care and clinical follow-up described in the Instructions for Use is recommended. The standard postoperative precautions described in the Instructions for Use, including activity restrictions and weight-bearing recommendations, should continue to be followed at the discretion of the treating surgeon. 1) Identify, and quarantine unused product and work with firm to facilitate product return. 2) Complete and return the attached Acknowledgement and Receipt Form 3) This recall notice should be shared with anyone who needs to be aware within your organization and forwarded to any organization where potentially affected devices have been transferred. Any product complaints should be reported to Orthofix at complaints@orthofix.com. For questions regarding this recall, including product return, replacement, or credit, please contact Audrey Mudderman, Senior Post Market Surveillance Specialist, at audreymudderman@orthofix.com
- K numbers
- K172130
- Harmonized identifiers (openFDA)
- Device name
- Filler, Bone Void, Calcium Compound
- Medical specialty description
- Orthopedic
- Regulation number
- 888.3045
- Device class
- 2
- K number
- K070437, K000122, K053213, K080065, K161859, K242372, K072384, K032409, K050025, K240424, K040419, K963562, K001724, K080511, K031838, K103799, K082338, K040454, K042340, K233259, K141956, K243706, K212991, K072444, K991854, K132071, K163621, K190956, K032268, K033679, K071004, K083232, K072170, K033722, K152071, K081717, K151584, K212721, K051123, K243609 +453 more
- Registration number
- 3005652161, 3013176080, 1417592, 3005304945, 3043620406, 1225991, 3003300673, 2029447, 3010097171, 9610921, 1000307092, 1000194445, 2029275, 3004111573, 1644312, 3009882464, 3012447612, 3008514120, 3014560508, 3010473074, 3016592693, 3004774118, 1030489, 3000215346, 3016851379, 3008522639, 1416980, 1833920, 3021988499, 3008110533, 1038671, 3006788678, 3009144915, 1319660, 1450662, 3008773560, 2531195, 1526439, 3012495575, 3014211822 +188 more
- FEI number
- 3002980729, 3002806315, 3005652161, 3013176080, 1417592, 3005304945, 3043620406, 3003300673, 3001237758, 3010097171, 1000194445, 1000307092, 3000215205, 3002807172, 1000117860, 3004111573, 3009882464, 3012447612, 3008514120, 3014560508, 3010473074, 3016592693, 3006813973, 3000215346, 3016851379, 3008522639, 1416980, 3021988499, 3002807113, 3008110533, 1038671, 3006788678, 3009144915, 1000518731, 1450662, 3008773560, 1526439, 3012495575, 3010813691, 3003870583 +188 more
