FDA Adverse Event Malfunction Summary report: N

SOL-MILLENNIUM

MDR report key: 22156671 · Received June 6, 2025

Report

Report Number
3014312726-2025-00126
Event Type
Malfunction
Date Received
June 6, 2025
Date of Event
May 9, 2025
Report Date
July 18, 2025
Manufacturer
SOL-MILLENNIUM MEDICAL INC
Product Code
FMF
UDI-DI
00840368503276
PMA / PMN Number
K153537
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
KS
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

OUR EVALUATION OF THE RISK, WHICH FOLLOWS GUIDANCE FROM ISO 14971, INDICATES THAT THE OVERALL RISK FOR THE REPORTED FAILURE IS LOW. THIS EVALUATION IS BASED ON OUR TRACK AND TREND ANALYSIS AND RISK MANAGEMENT FILES WHICH ARE EVALUATED AND UPDATED CONSTANTLY BASED ON POST MARKET SURVEILLANCE. ALL THE RETAINED SAMPLES AND CUSTOMER SAMPLES TESTED WERE WITHIN PRODUCT SPECIFICATION REQUIREMENTS AND NO EVIDENCE OF QUALITY ISSUES ASSOCIATED WITH THIS COMPLAINT. AS PART OF OUR CONTINUED COMMITMENT TO OUR CUSTOMERS, SOL MILLENNIUM WILL CONTINUE TO MONITOR THE COMPLAINTS TREND FOR THE REPORTED FAILURE MODE AND TAKE ANY CORRECTIVE ACTION BASED ON OUR PROCEDURES, IF A SIGNIFICANT PATTERN EMERGES. UNCONFIRMED.

Additional Manufacturer Narrative · 0

THIS SUPPLEMENTAL MDR IS BEING SUBMITTED TO CORRECT THE MANUFACTURING SITE INFORMATION PROVIDED IN THE INITIAL MDR 3014312726-2025-00126. THE PREVIOUSLY REPORTED MANUFACTURING SITE WAS INCORRECT. THE CORRECT MANUFACTURING SITE IS: PROMISEMED HANGZHOU MEDITECH CO., LTD.

Description of Event or Problem · 0

CUSTOMER REPORTED THAT THE PRODUCT LEAKAGE OF INSULIN SYRINGES AND ASK FOR RETURN GOODS OR RECALL.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1461696 SOL-MILLENNIUM SOL-M 1ML INSULIN SYRINGE W/FIXED NEEDLE 31G*8MM FMF SOL-MILLENNIUM MEDICAL INC 1613151BKM 07311044 00840368503276

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown