Orthofix U.S. LLC
Complete recall history across all FDA and CPSC categories, 9 total recalls
Orthofix U.S. LLC appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.
Device Recalls (9)
FDA medical device enforcement actions by Orthofix U.S. LLC
| Date | Product | Reason | Class |
|---|---|---|---|
| Jun 10, 2026 | Orthofix MINIRAIL, SHORT, LENGTHENER REF: M103, Unilateral orthopedic/trauma... | Unilateral external fixation devices may be incorrectly labeled. Minirail M10... | Class II |
| Jun 10, 2026 | Orthofix MINIRAIL, ARTICULATED, FIXATOR, VERTICAL AXIS REF: M122, Unilateral... | Unilateral external fixation devices may be incorrectly labeled. Minirail M10... | Class II |
| Jun 10, 2026 | Orthofix ARTICULATED MINIRAIL FIXATOR HORIZONTAL AXIS REF: M111, Unilateral ... | Unilateral external fixation devices may be incorrectly labeled. Minirail M10... | Class II |
| Jun 10, 2026 | Orthofix MINIRAIL, STANDARD LENGTHENER Model/Catalog Number: M101, Unilatera... | Unilateral external fixation devices may be incorrectly labeled. Minirail M10... | Class II |
| Nov 3, 2025 | Brand Name: FORZA" PTC Spacer System Product Name: FORZA" PTC Spacer System ... | Labeling contains claims that are not consistently present. | Class III |
| Nov 3, 2025 | Brand Name: Pillar" SA PTC Spacer System Product Name: Pillar" SA PTC Spacer... | Labeling contains claims that are not consistently present. | Class III |
| Nov 3, 2025 | Brand Name: FIREBIRD" SI Fusion System Product Name: FIREBIRD" SI Fusion Sys... | Labeling contains claims that are not consistently present. | Class III |
| Nov 3, 2025 | Brand Name: CONSTRUX" Mini PTC Spacer System Product Name: CONSTRUX" Mini PT... | Labeling contains claims that are not consistently present. | Class III |
| Nov 3, 2025 | Brand Name: CONSTRUX" Mini Ti Spacer System Product Name: CONSTRUX" Mini Ti ... | Labeling contains claims that are not consistently present. | Class III |
| Nov 3, 2025 | Brand Name: Forza" Ti Spacer System Product Name: Forza" Ti Spacer System M... | Labeling contains claims that are not consistently present. | Class III |
| Sep 19, 2025 | Virata Preassembled Polyaxial Screw, utilized in the Virata Spinal Fixation S... | Polyaxial screws do not meet performance standards. | Class II |
| Jun 24, 2025 | PILLAR SA Ti, STERILE, 37mm (W) x 28mm (D) x 18mm (H), 20-degrees, REF: 82-37... | A 37 mm implant width intervertebral body fusion device has a labeling discre... | Class II |
| Feb 20, 2025 | Orthofix Pillar SA Ti Spacer System Intervertebral Body Fusion Spinal Device,... | The product is mislabeled with the incorrect anterior height of 10mm, but the... | Class II |
Frequently Asked Questions
A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.
Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.
The FDA classifies recalls into three categories. Class I is the most serious, there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious, the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.
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