FDA Adverse Event Injury Summary report: N

PROCLAIM¿ 7 ELITE IMPLANTABLE PULSE GENERATOR

MDR report key: 18320690 · Received December 13, 2023

Report

Report Number
1627487-2023-05904
Event Type
Injury
Date Received
December 13, 2023
Date of Event
November 14, 2023
Report Date
December 13, 2023
Manufacturer
ABBOTT MEDICAL
Product Code
LGW
UDI-DI
05415067020222
PMA / PMN Number
P010032
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
AZ, US
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

DATE OF EVENT ESTIMATED. THE RESULTS OF THE INVESTIGATION ARE INCONCLUSIVE SINCE THE DEVICE WAS NOT RETURNED FOR ANALYSIS. BASED ON THE INFORMATION RECEIVED, THE CAUSE OF THE REPORTED EVENT COULD NOT BE CONCLUSIVELY DETERMINED. THE ALLEGATION IS AGAINST 1 OF 2 ANCHOR; HOWEVER, IT IS UNKNOWN WHICH ANCHOR(S), THEREFORE, ALL POTENTIAL COMPONENTS ARE BEING LISTED. ADDITIONAL COMPONENTS POTENTIALLY INVOLVED IN THE EVENT INCLUDE: COMMON DEVICE NAME: ANCHOR, MODEL: 1194ANS, UDI: (B)(4), SERIAL: N/A, BATCH: 6192367.

Description of Event or Problem · 0

RELATED MANUFACTURER REFERENCE NUMBER: 1627487-2023-05905. IT WAS REPORTED THAT THE PATIENT WAS EXPERIENCING DISCOMFORT AT THE IPG AND ANCHOR SITE. SURGICAL INTERVENTION TOOK PLACE WHERE THE IPG AND ANCHOR WERE EXPLANTED AND REPLACED TO ADDRESS THE ISSUE. EFFECTIVE STIMULATION WAS RESTORED. INVESTIGATION WAS UNABLE TO DETERMINE WHICH OF THE ANCHORS ATTRIBUTED TO THE EVENT. THE ALLEGATION IS AGAINST 1 OF 2 ANCHOR; HOWEVER, IT IS UNKNOWN WHICH ANCHOR(S), THEREFORE, ALL POTENTIAL COMPONENTS ARE BEING LISTED. ADDITIONAL COMPONENTS POTENTIALLY INVOLVED IN THE EVENT INCLUDE: COMMON DEVICE NAME: ANCHOR, MODEL: 1194ANS, UDI: (B)(4), SERIAL: N/A, BATCH: 6192367.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1655426 PROCLAIM¿ 7 ELITE IMPLANTABLE PULSE GENERATOR SCS IPG LGW ABBOTT MEDICAL 3662 6164970 05415067020222

Patients

Seq Age Sex Outcome Treatment
1 Male Other SCS ANCHOR| SCS LEAD (X2)