FDA Adverse Event Malfunction Summary report: N

AMSORB PLUS

MDR report key: 24176208 · Received January 26, 2026

Report

Report Number
3002226076-2026-01568
Event Type
Malfunction
Date Received
January 26, 2026
Date of Event
October 31, 2025
Report Date
January 26, 2026
Manufacturer
ARMSTRONG MEDICAL LTD
Product Code
CBL
PMA / PMN Number
9039632
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
501

Narratives

Additional Manufacturer Narrative · 0

ARMSTRONG MEDICAL LTD CONSIDER THIS CASE TO BE CLOSED.

Description of Event or Problem · 0

ARMSTRONG MEDICAL LTD RECEIVED A REPORT FROM GE HEALTHCARE (B)(4); (SIMILAR TO (B)(4) ON 31-OCT-2025. THE CUSTOMER, PCS CLINICAL ACCESSORIES (B)(6) FRANCE), RAISED AN ISSUE OCCURRING AT TWO DIFFERENT HOSPITALS WITH AMAB3801GE--, AMSORB PLUS PREFILLED G-CAN ABSORBER CANISTER, 1.0L, BOX OF 8 FOR THE SAME LOT 080425F211. LEAKS HAVE BEEN DETECTED ON ALL CUSTOMER BATCHES OF THESE SODA LIME CANISTERS. 3 BOXES CONCERNED LOT: 080425F211. PATIENT INVOLVEMENT BUT NO HARM REPORTED. ARMSTRONG MEDICAL LTD REQUESTED RETURN OF THE DEVICES, BUT THEY WERE NOT AVAILABLE TO RETURN. ARMSTRONG MEDICAL LTD WERE THEREFORE UNABLE TO INVESTIGATE A ROOT CAUSE RESULTING IN NO CORRECTIVE OR PREVENTIVE ACTION BEING DETERMINED OR IMPLEMENTED. ARMSTRONG MEDICAL WILL CONTINUE TO MONITOR THESE DEVICES AS PART OF OUR POST-MARKET SURVEILLANCE AND VIGILANCE ACTIVITIES. NOTE THAT THIS EVENT OCCURRED IN FRANCE, AS THE DEVICE IS AVAILABLE ON THE MARKET IN US, WE ARE OBLIGED TO NOTIFY THE FDA AS PER MDSAP REQUIREMENTS. AS THERE WAS PATIENT INVOLVEMENT WITH NO PATIENT HARM, ARMSTRONG MEDICAL LTD CONSIDER THIS TO BE A REPORTABLE EVENT AS IT MEETS ALL THREE BASIC REPORTING CRITERIA A-C OF MEDDEV 2 12-1 REV.8 AND MDR ARTICLE 2 (65).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
241269 AMSORB PLUS CARBON DIOXIDE ABSORBENT CBL ARMSTRONG MEDICAL LTD AMAB3801GE 080425F211

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown