FDA Adverse Event Malfunction Summary report: N

3.2MMX20MM RNGLC+ ACET DRL BIT

MDR report key: 12560998 · Received October 1, 2021

Report

Report Number
0001825034-2021-02789
Event Type
Malfunction
Date Received
October 1, 2021
Report Date
January 10, 2022
Manufacturer
ZIMMER BIOMET, INC.
Product Code
HTW
PMA / PMN Number
EXEMPT
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

(B)(4). DEVICE HISTORY RECORD (DHR) WAS REVIEWED AND NO DISCREPANCIES WERE FOUND. ROOT CAUSE WAS UNABLE TO BE DETERMINED. IF ANY FURTHER INFORMATION IS FOUND WHICH WOULD CHANGE OR ALTER ANY CONCLUSIONS OR INFORMATION, A SUPPLEMENTAL WILL BE FILED ACCORDINGLY. ZIMMER BIOMET WILL CONTINUE TO MONITOR FOR TRENDS.

Description of Event or Problem · 0

NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

Additional Manufacturer Narrative · 1

(B)(4). CUSTOMER HAS INDICATED THAT THE PRODUCT IS IN THE PROCESS OF BEING RETURNED TO ZIMMER BIOMET FOR INVESTIGATION. ONCE THE INVESTIGATION HAS BEEN COMPLETED A FOLLOW-UP MDR WILL BE SUBMITTED. CONCOMITANT PRODUCTS: PART # 31-323215/ ACET DRL BIT/ LOT # 355320. PART # 31-323230/ ACET DRL BIT/ LOT # 798150. PART # 31-323230 / ACET DRL BIT/ LOT # 232600. PART # 31-323215/ ACET DRL BIT/ LOT # 264520. REPORT SOURCE: (B)(6). MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS 0001825034 - 2021 - 02785, 0001825034 - 2021 - 02786, 0001825034 - 2021 - 02787, 0001825034 - 2021 - 02788.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE DRILL BITS WERE FRACTURED DURING DRILLING. NO ADVERSE CONSEQUENCES WERE REPORTED. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1458481 3.2MMX20MM RNGLC+ ACET DRL BIT INSTRUMENT, HIP HTW ZIMMER BIOMET, INC. NI 099920

Patients

Seq Age Sex Outcome Treatment
1 Unknown