Device recalls

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, ClassifiedProcess controlZ-2820-2026
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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
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.