FDA Adverse Event Malfunction Summary report: N

STEAM STER LOCKS ORANGE

MDR report key: 12975566 · Received December 10, 2021

Report

Report Number
2916714-2021-00232
Event Type
Malfunction
Date Received
December 10, 2021
Report Date
January 25, 2023
Manufacturer
AESCULAP INC.
Product Code
JOJ
UDI-DI
05055049091927
PMA / PMN Number
K890759
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

IF ADDITIONAL INFORMATION OR INVESTIGATION RESULTS BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.

Additional Manufacturer Narrative · 0

MANUFACTURER EVALUATION: THE DEVICE WAS NOT RETURNED TO THE MANUFACTURER FOR PHYSICAL EVALUATION. ADDITIONALLY, NO ON-SITE EVALUATION OF THE UNIT WAS PERFORMED AND NO PARTS WERE RETURNED FOR FAILURE ANALYSIS. THEREFORE, THE INVESTIGATION WAS NOT ABLE TO CONFIRM A DEVICE ISSUE THAT COULD BE ASSOCIATED WITH THE REPORTED EVENT. THE DEVICE HISTORY RECORDS (DHR) WERE NOT ABLE TO BE REVIEWED AS NO LOT NUMBER WAS MADE AVAILABLE. HOWEVER, ALL DEVICE HISTORY RECORDS (DHR) ARE REVIEWED AND RELEASED ACCORDING TO DOCUMENTED PROCEDURES AND A DEVICE IS NOT RELEASED IF IT DOES NOT MEET REQUIREMENTS OR IS NONCONFORMING. A DEFINITIVE CONCLUSION REGARDING THE COMPLAINT INCIDENT CANNOT BE REACHED WITHOUT A PHYSICAL EXAMINATION OF THE COMPLAINT DEVICE.

Description of Event or Problem · 0

IT WAS REPORTED THAT THERE WAS AN ISSUE WITH AN ORANGE INDICATOR. THE TAG WAS "FAULTY" AND FAILED THE STERILIZATION CYCLE. THERE WAS NO PATIENT INVOLVEMENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1878874 STEAM STER LOCKS ORANGE INDICATOR, PHYSICAL/CHEMICAL STERILIZATION PROCESS JOJ AESCULAP INC. US906 UNKNOWN 05055049091927
1878875 STEAM STER LOCKS ORANGE INDICATOR, PHYSICAL/CHEMICAL STERILIZATION PROCESS JOJ AESCULAP INC. US906 UNKNOWN 05055049091927

Patients

Seq Age Sex Outcome Treatment
1 Unknown