FDA Adverse Event Malfunction Summary report: N

AUTOPULSE® PLATFORM RESUSCITATION

MDR report key: 13502663 · Received February 9, 2022

Report

Report Number
3010617000-2022-00104
Event Type
Malfunction
Date Received
February 9, 2022
Report Date
February 9, 2022
Manufacturer
ZOLL CIRCULATION
Product Code
DRM
UDI-DI
00849111065009
PMA / PMN Number
K112998
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

HOLD FOR DD 2.11THE AUTOPULSE PLATFORM (SN (B)(4) INVOLVED IN THE REPORTED COMPLAINT WILL NOT BE RETURNED TO ZOLL FOR INVESTIGATION. BECAUSE AFTER THE REPORTED EVENT, THE CUSTOMER TESTED THE AUTOPULSE PLATFORM WITH ANOTHER LIFEBAND, AND THE PLATFORM FUNCTIONED AS INTENDED.

Description of Event or Problem · 0

DURING SHIFT CHECK, THE CUSTOMER INSTALLED LIFEBAND#1 (LOT #161862) TO TEST THE AUTOPULSE PLATFORM (SN (B)(4)). AFTER PERFORMING A FEW COMPRESSIONS, THE AUTOPULSE PLATFORM STOPPED WORKING WITH AN UNUSUAL SOUND AND DISPLAYED AN UNKNOWN ERROR MESSAGE. THE CUSTOMER OBSERVED THAT THE FABRIC HOLDING THE LIFEBAND BAND CLIP WAS TORN, AND THE BAND CLIP WAS DETACHED. THE CUSTOMER REPLACED IT WITH ANOTHER LIFEBAND #2 (LOT #161862) AND RESTARTED THE PLATFORM. SHORTLY AFTER COMPRESSION, THE HINGED BELT GUARD ON LIFEBAND GOT BROKEN WITH AN UNUSUAL SOUND. AFTER THE REPORTED ISSUE, THE CUSTOMER TESTED THE AUTOPULSE PLATFORM WITH ANOTHER LIFEBAND, AND THE PLATFORM FUNCTIONED AS INTENDED. NO PATIENT INVOLVEMENT. PLEASE SEE THE FOLLOWING RELATED MFR REPORT: MFR 3010617000-2022-00105 FOR THE LIFEBAND #1 (LOT #161862). MFR 3010617000-2022-00106 FOR THE LIFEBAND #2 (LOT #161862).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1850515 AUTOPULSE® PLATFORM RESUSCITATION CARDIAC CHEST COMPRESSOR DRM ZOLL CIRCULATION MODEL 100 00849111065009

Patients

Seq Age Sex Outcome Treatment
1 Unknown