CONSTRUX - MINI PTC recallZ-0891-2026 · Orthofix U.S. LLC · initiated Nov 3, 2025
Open, Classified
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Orthofix U.S. LLC or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
Labeling contains claims that are not consistently present.
FDA root cause category: Device Design
What the company is doing
On November 3, 2025 Orthofix issued a recall notification via Email to affected consignees. In addition to informing consignees about the recall , Orthofix ask consignees to take the following actions: 1. Orthofix is removing claims regarding Nanovate Technology in materials, including but not limited to Operative Techniques, Product Brochures, Medical Education Documents, and the Orthofix website. 2. No product return is being requested. You may continue to use the product. 3. Distribute this Notice to all relevant personnel within your organization. 4. Forward this Notice to other organization or facilities where affected products may have been transferred. 5. Acknowledge this Notice and return the completed receipt form to [email protected]
Recall details
- Recall number
- Z-0891-2026
- Status
- Open, Classified
- Initiated by the company
- Nov 3, 2025
- Posted by the FDA
- Dec 11, 2025
- Recalling firm
- Orthofix U.S. LLC
- Quantity
- 61977
- Product code
- ODP
- FDA submissions
- K172437
- Distribution
- Worldwide - US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, ND, NE, NH, NJ, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, WA, WI, WY and the countries of AU, DE, PR, GB, HU, CZ, CA, CL, AE, ZA, BR.
Product description
Brand Name: CONSTRUX" Mini PTC Spacer System Product Name: CONSTRUX" Mini PTC Spacer System Model/Catalog Number: 37-3106SP 12mm W X 12mm L, 6mm H, Parallel; 37-3107SP 12mm W X 12mm L, 7mm H, Parallel; 37-3108SP 12mm W X 12mm L, 8mm H, Parallel; 37-3109SP 12mm W X 12mm L, 9mm H, Parallel; 37-3110SP 12mm W X 12mm L, 10mm H, Parallel; 37-3111SP 12mm W X 12mm L, 11mm H, Parallel; 37-3112SP 12mm W X 12mm L, 12mm H, Parallel; 37-3113SP 12mm W X 12mm LW, 13mm H, Parallel; 37-3114SP 12mm W X 12mm WL, 14mm H, Parallel; 37-3006SP 12mm W X 12mm L, 6mm H, 5 Lordotic; 37-3007SP 12mm W X 12mm L, 7mm H, 5 Lordotic; 37-3008SP 12mm W X 12mm L, 8mm H, 5 Lordotic; 37-3009SP 12mm WL X 12mm L, 9mm H, 5 Lordotic; 37-3010SP 12mm W X 12mm L, 10mm H, 5 Lordotic; 37-3011SP 12mm W X 12mm L, 11mm H, 5 Lordotic; 37-3012SP 12mm W X 12mm L, 12mm H, 5 Lordotic; 37-3013SP 12mm W X 12mm L, 13mm H, 5 Lordotic; 37-3014SP 12mm W X 12mm L, 14mm H, 5 Lordotic; 37-3207SP 12mm W X 12mm L, 7mm H, 10 Lordotic; 37-3208SP 12mm W X 12mm L, 8mm H, 10 Lordotic; 37-3209SP 12mm W X 12mm L, 9mm H, 10 Lordotic; 37-3210SP 12mm W X 12mm L, 10mm H, 10 Lordotic; 37-3211SP 12mm W X 12mm L, 11mm H, 10 Lordotic; 37-3212SP 12mm W X 12mm L, 12mm H, 10 Lordotic; 37-4106SP 15mm W X 12mm L, 6mm H, Parallel; 37-4107SP 15mm W X 12mm L, 7mm H, Parallel; 37-4108SP 15mm W X 12mm L, 8mm H, Parallel; 37-4109SP 15mm W X 12mm L, 9mm H, Parallel; 37-4110SP 15mm W X 12mm L, 10mm H, Parallel; 37-4111SP 15mm W X 12mm L, 11mm H, Parallel; 37-4112SP 15mm W X 12mm L, 12mm H, Parallel; 37-4113SP 15mm W X 12mm L, 13mm H, Parallel; 37-4114SP 15mm W X 12mm L, 14mm H, Parallel; 37-4006SP 15mm W X 12mm L, 6mm H, 5 Lordotic; 37-4007SP 15mm W X 12mm L, 7mm H, 5 Lordotic; 37-4008SP 15mm W X 12mm L, 8mm H, 5 Lordotic; 37-4009SP 15mm W X 12mm L, 9mm H, 5 Lordotic; 37-4010SP 15mm W X 12mm L, 10mm H, 5 Lordotic; 37-4011SP 15mm W X 12mm L, 11mm H, 5 Lordotic; 37-4012SP 15mm W X 12mm L, 12mm H, 5 Lordotic; 37-4013SP 15mm W X 12mm L, 13mm H, 5 Lordotic; 37-4014SP 15mm W X 12mm L, 14mm H, 5 Lordotic; 37-4207SP 15mm W X 12mm L, 7mm H, 10 Lordotic; 37-4208SP 15mm W X 12mm L, 8mm H, 10 Lordotic; 37-4209SP 15mm W X 12mm L, 9mm H, 10 Lordotic; 37-4210SP 15mm W X 12mm L, 10mm H, 10 Lordotic; 37-4211SP 15mm W X 12mm L, 11mm H, 10 Lordotic; 37-4212SP 15mm W X 12mm L, 12mm H, 10 Lordotic; 37-5106SP 15mm W X 15mm L, 6mm H, Parallel; 37-5107SP 15mm W X 15mm L, 7mm H, Parallel 37-5108SP 15mm W X 15mm L, 8mm H, Parallel; 37-5109SP 15mm W X 15mm L, 9mm H, Parallel; 37-5110SP 15mm W X 15mm L, 10mm H, Parallel; 37-5111SP 15mm W X 15mm L, 11mm H, Parallel; 37-5112SP 15mm W X 15mm L, 12mm H, Parallel; 37-5113SP 15mm W X 15mm L, 13mm H, Parallel; 37-5114SP 15mm W X 15mm L, 14mm H, Parallel; 37-5006SP 15mm W X 15mm L, 6mm H, 5 Lordotic; 37-5007SP 15mm W X 15mm L, 7mm H, 5 Lordotic; 37-5008SP 15mm W X 15mm L, 8mm H, 5 Lordotic; 37-5009SP 15mm W X 15mm L, 9mm H, 5 Lordotic; 37-5010SP 15mm W X 15mm L, 10mm H, 5 Lordotic; 37-5011SP 15mm W X 15mm L, 11mm H, 5 Lordotic; 37-5012SP 15mm W X 15mm L, 12mm H, 5 Lordotic; 37-5013SP 15mm W X 15mm L, 13mm H, 5 Lordotic; 37-5014SP 15mm W X 15mm L, 14mm H, 5 Lordotic; 37-5207SP 15mm W X 15mm L, 7mm H, 10 Lordotic; 37-5208SP 15mm W X 15mm L, 8mm H, 10 Lordotic; 37-5209SP 15mm W X 15mm LW, 9mm H, 10 Lordotic; 37-5210SP 15mm W X 15mm L, 10mm H, 10 Lordotic; 37-5211SP 15mm W X 15mm L, 11mm H, 10 Lordotic; 37-5212SP 15mm W X 15mm L, 12mm H, 10 Lordotic;
Code information (models, lots, serial numbers)
Show the full code information (2k characters)
Lot Code: All Lots/ UDI: 37-3106SP 18257200030590 37-3107SP 18257200030613 37-3108SP 18257200030637 37-3109SP 18257200030651 37-3110SP 18257200030675 37-3111SP 18257200030699 37-3112SP 18257200030712 37-3113SP 18257200030736 37-3114SP 18257200030750 37-3006SP 18257200030415 37-3007SP 18257200030439 37-3008SP 18257200030453 37-3009SP 18257200030477 37-3010SP 18257200030491 37-3011SP 18257200030514 37-3012SP 18257200030538 37-3013SP 18257200030552 37-3014SP 18257200030576 37-3207SP 18257200146352 37-3208SP 18257200146369 37-3209SP 18257200146376 37-3210SP 18257200146383 37-3211SP 18257200146390 37-3212SP 18257200146406 37-4106SP 18257200030958 37-4107SP 18257200030972 37-4108SP 18257200030996 37-4109SP 18257200031016 37-4110SP 18257200031030 37-4111SP 18257200031054 37-4112SP 18257200031078 37-4113SP 18257200031092 37-4114SP 18257200031115 37-4006SP 18257200030774 37-4007SP 18257200030798 Part Number GTIN 37-4008SP 18257200030811 37-4009SP 18257200030835 37-4010SP 18257200030859 37-4011SP 18257200030873 37-4012SP 18257200030897 37-4013SP 18257200030910 37-4014SP 18257200030934 37-4207SP 18257200146420 37-4208SP 18257200146437 37-4209SP 18257200146444 37-4210SP 18257200146451 37-4211SP 18257200146468 37-4212SP 18257200146475 37-5106SP 18257200031313 37-5107SP 18257200031337 37-5108SP 18257200031351 37-5109SP 18257200031375 37-5110SP 18257200031399 37-5111SP 18257200031412 37-5112SP 18257200031436 37-5113SP 18257200031450 37-5114SP 18257200031474 37-5006SP 18257200031139 37-5007SP 18257200031153 37-5008SP 18257200031177 37-5009SP 18257200031191 37-5010SP 18257200031214 37-5011SP 18257200031238 37-5012SP 18257200031252 37-5013SP 18257200031276 37-5014SP 18257200031290 37-5207SP 18257200146505 37-5208SP 18257200146512 37-5209SP 18257200146529 37-5210SP 18257200146536 37-5211SP 18257200146543 37-5212SP 18257200146550
Devices named in this recall
70 devices in the FDA device registry whose identifier appears in the recall's code information.
- CONSTRUX - MINI PTC 37-3006SPOrthofix US LLC · Intervertebral Fusion Device With Bone Graft, Cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-3007SPOrthofix US LLC · Intervertebral Fusion Device With Bone Graft, Cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-3008SPOrthofix US LLC · Intervertebral Fusion Device With Bone Graft, Cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-3009SPOrthofix US LLC · Intervertebral Fusion Device With Bone Graft, Cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-3010SPOrthofix US LLC · Intervertebral Fusion Device With Bone Graft, Cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-3011SPOrthofix US LLC · Intervertebral Fusion Device With Bone Graft, Cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-3012SPOrthofix US LLC · Intervertebral Fusion Device With Bone Graft, Cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-3013SPOrthofix US LLC · Intervertebral Fusion Device With Bone Graft, Cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-3014SPOrthofix US LLC · Intervertebral Fusion Device With Bone Graft, Cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-3106SPOrthofix US LLC · Intervertebral Fusion Device With Bone Graft, Cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-3107SPOrthofix US LLC · Intervertebral Fusion Device With Bone Graft, Cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-3108SPOrthofix US LLC · Intervertebral Fusion Device With Bone Graft, Cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-3109SPOrthofix US LLC · Intervertebral Fusion Device With Bone Graft, Cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-3110SPOrthofix US LLC · Intervertebral Fusion Device With Bone Graft, Cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-3111SPOrthofix US LLC · Intervertebral Fusion Device With Bone Graft, Cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-3112SPOrthofix US LLC · Intervertebral Fusion Device With Bone Graft, Cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-3113SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-3114SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-4006SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-4007SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-4008SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-4009SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-4010SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-4011SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-4012SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-4013SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-4014SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-4106SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-4107SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-4108SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-4109SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-4110SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-4111SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-4112SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-4113SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-4114SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-5006SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-5007SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-5008SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-5009SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-5010SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-5011SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-5012SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-5013SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-5014SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-5106SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-5107SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-5108SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-5109SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-5110SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-5111SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-5112SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-5113SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-5114SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-3208SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-3209SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-3210SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-3211SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-3212SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-4207SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-4208SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-4209SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-4211SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-4212SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-5207SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-5208SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-5209SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-5210SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-5211SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
- CONSTRUX - MINI PTC 37-5212SPOrthofix US LLC · Intervertebral fusion device with bone graft, cervical1 recall0 reports
Product lines
Other devices under the same FDA submission
92 devices cleared under K172437 are not named by identifier in this recall. One submission often covers many models, so they may or may not be affected.
- FORZA PTC 38-3011SPOrthofix US LLC · Intervertebral fusion device with bone graft, lumbar1 recall1 report
- FORZA PTC 38-1709SPOrthofix US LLC · Intervertebral fusion device with bone graft, lumbar1 recall1 report
- FORZA PTC 38-1711SPOrthofix US LLC · Intervertebral fusion device with bone graft, lumbar1 recall1 report
- FORZA PTC 38-1007SPOrthofix US LLC · Intervertebral fusion device with bone graft, lumbar1 recall0 reports
- FORZA PTC 38-1008SPOrthofix US LLC · Intervertebral fusion device with bone graft, lumbar1 recall0 reports
- FORZA PTC 38-1009SPOrthofix US LLC · Intervertebral fusion device with bone graft, lumbar1 recall0 reports
- FORZA PTC 38-1011SPOrthofix US LLC · Intervertebral fusion device with bone graft, lumbar1 recall0 reports
- FORZA PTC 38-1012SPOrthofix US LLC · Intervertebral fusion device with bone graft, lumbar1 recall0 reports
- FORZA PTC 38-1013SPOrthofix US LLC · Intervertebral fusion device with bone graft, lumbar1 recall0 reports
- FORZA PTC 38-1014SPOrthofix US LLC · Intervertebral fusion device with bone graft, lumbar1 recall0 reports
- FORZA PTC 38-7008SPOrthofix US LLC · Intervertebral fusion device with bone graft, lumbar1 recall0 reports
- FORZA PTC 38-7009SPOrthofix US LLC · Intervertebral fusion device with bone graft, lumbar1 recall0 reports
Other products in the same recall event
The FDA groups related products into one recall event (event 97862).
- Z-0892-2026 · Open, ClassifiedBrand Name: FORZA" PTC Spacer System Product Name: FORZA" PTC Spacer System Model/Catalog Number: 38-1007SP FORZA PTC Spacer, Straight, 0, 9W x 23L x 7H 38-1008SP FORZA PTC Spacer,…
- Z-0893-2026 · Open, ClassifiedBrand Name: Pillar" SA PTC Spacer System Product Name: Pillar" SA PTC Spacer System Model/Catalog Number: 39-9012SP 33W X 28L X 12.5H, 7DEG PTC IMPLANT; 39-9014SP 33W X 28L X 14H, …
- Z-0894-2026 · Open, ClassifiedBrand Name: FIREBIRD" SI Fusion System Product Name: FIREBIRD" SI Fusion System Model/Catalog Number: 18-1025SP 11mm X 25mm FIREBIRD SI Screw; 18-1030SP 11mm X 30mm FIREBIRD SI Scr…
- Z-0895-2026 · Open, ClassifiedBrand Name: Forza" Ti Spacer System Product Name: Forza" Ti Spacer System Model/Catalog Number: 38-2006SP FORZA Ti Spacer, Straight, 0, 9W x 23L x 6H; 38-2007SP FORZA Ti Spacer, St…
- Z-0896-2026 · Open, ClassifiedBrand Name: CONSTRUX" Mini Ti Spacer System Product Name: CONSTRUX" Mini Ti Spacer System Model/Catalog Number: 37-6005SP 12mm W X 12mm L, 5mm H, 5 Lordotic 37-6005SP 12mm W X 12…
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
How recalls are matched to devices · Editorial policy · Report an error on this page