STALIF C-Ti C146551-3TcRecalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00815101028668), received between Jul 15, 2019 and Aug 6, 2019 — classified as 4 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (4 reports).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• InjuryAug 6, 2019Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information; Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information

  PATIENT EMAILED MANUFACTURER DIRECTLY INDICATING THEY RECEIVED A REVISION SURGERY AT THE LEVEL OF THE STALIF C-TI CONSTRUCT ON (B)(6) 2018. THE PATIENT ALSO INDICATED THEY ARE HAVING SIDE EFFECTS THEY ATTRIBUTED TO THE STALIF C-TI CAGE AND/OR STALIF C ABO SCREWS. THE PATIENT HAS INDICATED THEY WERE INSTRUCTED BY THEIR SPINE SURGEON TO SEEK THE CARE OF AN ALLERGIST. THE PATIENT FURTHER DETAILED THEIR SYMPTOMS AS BEING: SWELLING OF THROAT, WRISTS, BURNING SENSATION, DIFFICULTY BREATHING, DIFFICULTY SWALLOWING, CHOKING HAZARD, FOOD GOING INTO THE AIRWAY, REDNESS, AND OTHER NON-SPECIFIED ISSUES.

  Patient problems: Burning Sensation; Dysphagia/ Odynophagia; Foreign Body Sensation in Eye; Neck Pain; Swollen Lymph Nodes

  MAUDE report 8866269 ↗
• InjuryAug 6, 2019Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information; Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information

  PATIENT EMAILED MANUFACTURER DIRECTLY INDICATING THEY RECEIVED A REVISION SURGERY AT THE LEVEL OF THE STALIF C-TI CONSTRUCT ON (B)(6) 2018. THE PATIENT ALSO INDICATED THEY ARE HAVING SIDE EFFECTS THEY ATTRIBUTED TO THE STALIF C-TI CAGE AND/OR STALIF C ABO SCREWS. THE PATIENT HAS INDICATED THEY WERE INSTRUCTED BY THEIR SPINE SURGEON TO SEEK THE CARE OF AN ALLERGIST. THE PATIENT FURTHER DETAILED THEIR SYMPTOMS AS BEING: SWELLING OF THROAT, WRISTS, BURNING SENSATION, DIFFICULTY BREATHING, DIFFICULTY SWALLOWING, CHOKING HAZARD, FOOD GOING INTO THE AIRWAY, REDNESS, AND OTHER NON-SPECIFIED ISSUES.

  Patient problems: Burning Sensation; Dysphagia/ Odynophagia; Foreign Body Sensation in Eye; Neck Pain; Swollen Lymph Nodes

  MAUDE report 8865622 ↗
• InjuryJul 15, 2019Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information; Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information

  PATIENT EMAILED MANUFACTURER DIRECTLY INDICATING THEY RECEIVED A REVISION SURGERY AT THE LEVEL OF THE STALIF C-TI CONSTRUCT ON (B)(6) 2018. THE PATIENT ALSO INDICATED THEY ARE HAVING SIDE EFFECTS THEY ATRIBUTED TO THE STALIF C-TI CAGE AND/OR STALIF C ABO SCREWS. THE PATIENT HAS INDICATED THEY WERE INSTRUCTED BY THEIR SPINE SURGEON TO SEEK THE CARE OF AN ALLERGIST. THE PATIENT FURTHER DETAILED THEIR SYMPTOMS AS BEING: SWELLING OF THROAT, WRISTS, BURNING SENSATION, DIFFICULTY BREATHING, DIFFICULTY SWALLOWING, CHOKING HAZARD, FOOD GOING INTO THE AIRWAY, REDNESS, AND OTHER NON-SPECIFIED ISSUES.

  Patient problems: Burning Sensation; Dysphagia/ Odynophagia; Foreign Body Sensation in Eye; Neck Pain; Swollen Lymph Nodes

  MAUDE report 8791127 ↗
• InjuryJul 15, 2019Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information; Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information

  PATIENT EMAILED MANUFACTURER DIRECTLY INDICATING THEY RECEIVED A REVISION SURGERY AT THE LEVEL OF THE STALIF C-TI CONSTRUCT ON (B)(6) 2018. THE PATIENT ALSO INDICATED THEY ARE HAVING SIDE EFFECTS THEY ATTRIBUTED TO THE STALIF C-TI CAGE AND/OR STALIF C ABO SCREWS. THE PATIENT HAS INDICATED THEY WERE INSTRUCTED BY THEIR SPINE SURGEON TO SEEK THE CARE OF AN ALLERGIST. THE PATIENT FURTHER DETAILED THEIR SYMPTOMS AS BEING: SWELLING OF THROAT, WRISTS, BURNING SENSATION, DIFFICULTY BREATHING, DIFFICULTY SWALLOWING, CHOKING HAZARD, FOOD GOING INTO THE AIRWAY, REDNESS, AND OTHER NON-SPECIFIED ISSUES.

  Patient problems: Burning Sensation; Dysphagia/ Odynophagia; Foreign Body Sensation in Eye; Neck Pain; Swollen Lymph Nodes

  MAUDE report 8791125 ↗