Manufacturer
3 recalls in our database name RTI Surgical, Inc. as the manufacturing or recalling firm.
Of the 3 recalls from RTI Surgical, Inc. we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.
The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.
Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.
RTI Surgical is recalling 24 units of BioSet IC RT Paste due to incorrect instructions for use. The product was distributed in Colombia.
RTI Surgical, Inc. is recalling 14 units of OPTEFORM Allograft Paste 5cc because they may contain a 10cc fluid dispenser with incorrect fill lines.
RTI Surgical is recalling 1,906 C-Plus 10mm x 12mm Webless implants because they were incorrectly documented as meeting labeling requirements for a partial Vertebral Body Replacement Device.
Community-sourced company facts from Wikidata, not from any recall agency. This is background on the corporate entity — it says nothing about the recall(s) listed on this page, which come from the agency source notice above.
RTI Surgical (United States)
company in Alachua, United States
Source: Wikidata (Q30255300), licensed CC0. Wikidata is community-edited and may not reflect the current corporate structure.