AMSORB PLUS CARBON DIOXIDE ABSORBER, 1.2 LITERS AMAB4001

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-04-03 for AMSORB PLUS CARBON DIOXIDE ABSORBER, 1.2 LITERS AMAB4001 manufactured by Armstrong Medical Ltd..

Event Text Entries

[42309136] A new (to our facility) product, an amsorb plus carbon dioxide absorber, was installed in all four of our operating rooms, 4 identical drager apollo anesthesia machines. In one of the four rooms, during the first 6 hours of use, a crack developed in the top of the amsorb plus absorber casing at the point where a dual flange inserts into the drager apollo machine. This crack, which exceeded 50 liters of fresh gas flow per minute, made positive pressure ventilation (by ventilator or by hand) of an anesthetized pt impossible. Several items are worthy of note: the machine had passed its automated routine daily checkout at 6am. A surgery performed from 0730 to 1000 had no problems with ventilation. Prior to the event surgery, the excessive leak was identified during a routine abbreviated "between surgeries" check out. The leak was not audible or visible (until the amsorb plus canister was removed from the machine); the leak stopped the anesthetic induction process. In an emergency, an abbreviated pressure check would not be performed and the pt would have been anesthetized and positive pressure ventilation would not have been possible. We tested the same amsorb plus product in 2015 and had an identical crack and leak on the first day of use. We asked the manufacturer to improve the strength of the plastic flange at the top of the absorber and did not use the product again until (b)(6) 2016. We have used a different brand of absorber (drager brand) on these drager apollo anesthesia machines for the past 9 years (x 4 rooms = more than 10000 man-days of use) and have never had a single crack or leak of this type. The plastic flange of the amsorb plus absorber is palpably less compliant and more brittle versus the drager brand absorber. Significant stress is placed on the plastic flange of either absorber during installation ("snap into position") and when the absorber is bumped during routine use (bumped by a chair, blood warmer, knee, etc). We spoke with the manufacturer representative in 2015 and on 03/31/2016 and demonstrated the brittleness of the plastic housing of the amsorb plus absorber vs the drager absorber product. The brittle plastic flange of the amsorb plus absorber can be broken with two fingers. The compliant, flexible flange of the drager absorber product cannot be broken with two fingers. The most important finding is that we had two events - one year apart - in two days of use, versus the drager absorber product which has been used for 9 years with no incidents. Last year, we returned the product to the manufacturer; this year, we kept it. The absorber was exposed to routine anesthetic agents for less than 6 hours - on two different occasions with two different anesthesiologists - and developed a potentially life threatening crack and leak in less than 6 hours of use.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW5061519
MDR Report Key5553764
Date Received2016-04-03
Date of Report2016-04-03
Date of Event2016-03-31
Date Added to Maude2016-04-07
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameAMSORB PLUS CARBON DIOXIDE ABSORBER, 1.2 LITERS
Generic NameAMSORB PLUS UNIVERSAL BUBBLE CAN
Product CodeBSF
Date Received2016-04-03
Model NumberAMAB4001
Lot Number150216F33
Device Expiration Date2019-01-31
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerARMSTRONG MEDICAL LTD.
Manufacturer AddressCOLERAINE BT521BS EI BT52 1BS


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2016-04-03

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.