MAUDE Adverse Event Report: Merit Maquiladora Mexico TEMNO¿; Biopsy Needle Kit

Catalog Number	CT1411
Medical Device Problem Code	Insufficient Device Problem Information (3190)
Health Effect - Clinical Code	Pneumothorax (2012)
Date of Event	08/01/2022
Type of Reportable Event	Serious Injury

• Brand Name: TEMNO¿
• Common Device Name: Biopsy Needle Kit
• Manufacturer (Section D): Merit Maquiladora Mexico; avenida sor juana ines de; 19970 interior b, edificio 2; tijuana baja california 22630 ; MX 22630
• Manufacturer (Section G): Merit Maquiladora Mexico; avenida sor juana ines de; 19970 interior b, edificio 2; tijuana baja california 22630 ; MX 22630
• Manufacturer Contact: lisa perz msn, rn, pmp ; 1600 merit parkway; south jordan, UT 84095 ; +1(801)208-4225
• MDR Report Key: 50892023
• Report Number: 3011642792-2026-00230
• Device Sequence Number: 20340152
• Product Code: FCG
• UDI-Device Identifier: 00884450444115
• UDI-Public: 00884450444115
• Combination Product (Y/N): N
• Initial Reporter State: MI
• Initial Reporter Country: US
• PMA/510(K) Number: K902319
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Literature,Company Representative
• Type of Report: Initial
• Report Date (Section B): 09/24/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Catalogue Number: CT1411
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 08/27/2026
• Initial Report FDA Received Date: 09/24/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Is the Device Labeled for Single Use? (Y/N): Yes
• Usage of Device: Initial
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention; Other
• Patient Sex: Unknown