BIOROOT RCS 01E0300

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2017-10-23 for BIOROOT RCS 01E0300 manufactured by Septodont, Inc..

Event Text Entries

[89961904] Spontaneous report, (b)(4). Initial information received on 21-sep-2017 from the dentist by phone. The dentist reported that a (b)(6) female patient, with medical history of allergy multiple, penicillin and aspirin allergy, dental fistula and broken tooth #21, received an unknown dose of the suspected septanest 40 mg/ml with adrenaline 1/200. 000 solution for injection (articaine hydrochloride; epinephrine bitartrate), by dental route for local anaesthesia before a root canal procedure with the medical device bioroot rcs (batch b18997, exp 08/2018), on (b)(6) 2017. The patient had previously been treated with septanest 40 mg/ml with adrenaline 1/200. 000, without complications. On (b)(6) 2017, at the end of dental procedure, the dentist noted a gingival swelling without inflammatory reaction (no redness), and the patient experienced soft tissue necrosis rather whitish appearance. During the root canal treatment, the dentist used a disinfectant (paroex) for cleaning the root, without reaction of the patient. The dentist confirmed there was no periapical extrusion of product. On (b)(6) 2017, the dentist saw again the patient and extension of swelling from cheek to eye was noted. The dentist removed the medical device bioroot rcs, and prescribed an anti inflammatory, flanid (tiaprofenic) and an homeopathic treatment with apis mellifica. Posology and therapy duration were not provided. At the time of this report, the patient was recovering. An interview was planned within 2 weeks. The dentist suspected an allergic reaction to the medical device bioroot rcs. Additional information received on 25-sep-2017 from the dentist by phone provided regarding patient's outcome, no periapical overfilling was done, and trade name of disinfectant used during dental treatment. Causality assessment on 29-sep-2017 on initial information received on 21-sep-2017: seriousness: serious (ime list term > other medically important condition). Listedness/expectedness: soft tissue necrosis: unexpected eu/us/ca; facial swelling: unexpected eu/us/ca. Gingival swelling: unexpected eu/us/ca. Causality: latency: suggestive, recognized association: no, analysis: in this case, swelling and local reaction occurred after the dental procedure. Swelling after root canal treatment is described, and these reactions are probably related to the endodontic procedure including shaping, canal irrigation and canal filling. However in this patient with medical history of multiple allergies, product hypersensitivity cannot be excluded. Moreover since patient recovered after removal of the cement, the causality between bioroot and facial and gingival swelling was assessed as possible. Regarding soft tissue necrosis, the local injection with vasoconstrictor may be an etiology but very few information is provided regarding this reaction and outcome was unknown. This must be a complication of dental fistula and abscess which seems the most probably etiology. Therefore, the causality between bioroot and soft tissue necrosis was assessed as unlikely. Dechallenge: na, rechallenge: na. Concluded causality who: unlikely for soft tissue necrosis, possible for facial swelling and gingival swelling.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0001721729-2017-00010
MDR Report Key6968516
Report SourceFOREIGN,HEALTH PROFESSIONAL
Date Received2017-10-23
Date of Report2017-10-20
Date of Event2017-09-20
Date Mfgr Received2017-10-04
Date Added to Maude2017-10-23
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional0
Initial Report to FDA0
Report to FDA3
Event Location3
Manufacturer ContactMR. LAWRENCE KASS
Manufacturer Street416 SOUTH TAYLOR AVE.
Manufacturer CityLOUISVILLE CO 80027
Manufacturer CountryUS
Manufacturer Postal80027
Manufacturer Phone3036657535
Manufacturer G1SEPTODONT INC.
Manufacturer Street416 SOUTH TAYLOR AVE.
Manufacturer CityLOUISVILLE CO 80027
Manufacturer CountryUS
Manufacturer Postal Code80027
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBIOROOT RCS
Generic NameBIOROOT RCS
Product CodeKIF
Date Received2017-10-23
Model Number01E0300
Lot NumberB18997
Device Expiration Date2018-08-31
OperatorDENTIST
Device Availability*
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSEPTODONT, INC.
Manufacturer Address416 S. TAYLOR AVENUE LOUISVILLE CO 80270 US 80270


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2017-10-23

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.