PROCLAIM¿ 7 ELITE IMPLANTABLE PULSE GENERATOR
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
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.
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) |