FDA Adverse Event Malfunction Summary report: N

PRIMETAPER DRILL SLEEVE 5WD GS

MDR report key: 24784351 · Received April 4, 2026

Report

Report Number
3013111692-2026-10981
Event Type
Malfunction
Date Received
April 4, 2026
Date of Event
March 13, 2026
Report Date
April 3, 2026
Manufacturer
DENTSPLY IMPLANTS MANUFACTURING GMBH
Product Code
NDP
UDI-DI
07392532269981
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
UK
Reporter Occupation
DENTIST
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

THERE HAS BEEN A PREVIOUS REPORT RECEIVED WHERE THIS MALFUNCTION RESULTED IN A SERIOUS INJURY. THEREFORE, IT MUST BE PRESUMED THAT RECURRENCE OF THIS MALFUNCTION COULD POSSIBLY CAUSE OR CONTRIBUTE TO A SERIOUS INJURY OR REQUIRE MEDICAL OR SURGICAL INTERVENTION TO PRECLUDE SUCH. AS SUCH, THIS EVENT IS REPORTABLE PER 21CFR PART 803. PRODUCTS RETURN IS REQUESTED AND WILL BE EVALUATED AFTER RECEIPT. IN CASE ANY NEW OR ADDITIONAL INFORMATION WILL BE GAINED FROM THIS INVESTIGATION A FOLLOW-UP REPORT WILL BE SENT. TREND IS TRACKED AND MONITORED.

Description of Event or Problem · 0

CUSTOMER REPORTED LOSS OF INTERNAL SPRING WITHIN THE DRILL SLEEVE. 2026-03-12 DIOGP514: SPRING RING ISSUE ¿ CAPA NUMBER 2025-58. EVENT DEEMED NOT REPORTABLE IN COUNTRIES OTHER THAT THE US AS FOLLOW: EU: IT DOES NOT MEET THE CRITERIA OF A SERIOUS INCIDENT AND REFLECTS A DOCUMENTED INHERENT DEVICE RISK; THE EVENT IS DEEMED NOT REPORTABLE TO THE CA BUT WILL BE DOCUMENTED AND MONITORED THROUGH POST-MARKET SURVEILLANCE. BR: NOT MARKETED/ RELEASED. AU: THE EVENT OCCURRED OVERSEAS. CA: EVENT OCCURRED IN A FOREIGN COUNTRY WITH A CLASS II DEVICE. CN: THE EVENT DID NOT CAUSE A DEATH, NOR SEVERE INJURIES OR COULD HAVE POSSIBLY CAUSED SEVERE INJURIES/DEATH AND NO SERIOUS PUBLIC HEALTH THREAT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
846966 PRIMETAPER DRILL SLEEVE 5WD GS ACCESSORIES, IMPLANT, DENTAL, ENDOSSEOUS NDP DENTSPLY IMPLANTS MANUFACTURING GMBH 540916 07392532269981

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Required Intervention NOT PROVIDED.