Device recalls

Vercise Genus Deep Brain Stimulation (DBS) Implantable Pulse Generator IPG: R16 IPG KIT, REF: M365DB12160, and R32 IPG KIT, REF: M365DB12320

Boston Scientific Neuromodulation Corporation · Deep Brain Stimulation (DBS) Implantable Pulse Generator (IPG) may experience routine system check during IPG charging, which may cause device reset. The devic…

Open, ClassifiedDevice DesignZ-1890-2024
Open FDA's page for this record
Cfres ID
207089
Product res number
Z-1890-2024
Event date initiated
2024-04-18
Event date posted
2024-05-24
Recall status
Open, Classified
Res event number
94377
Product code
NHL
Product description
Vercise Genus Deep Brain Stimulation (DBS) Implantable Pulse Generator IPG: R16 IPG KIT, REF: M365DB12160, and R32 IPG KIT, REF: M365DB12320
Firm FEI number
3006630150
Recalling firm
Boston Scientific Neuromodulation Corporation
Address 1
25155 Rye Canyon Loop
City
Valencia
State
CA
Postal code
91355-5004
Additional info contact
Rebecca KinKead Rubio 651-581-0761
Root cause description
Device Design
Product quantity
14,977
Code info

REF/UDI-DI(GTIN)/Serial Number Range/Expiration Date Range: M365DB12160/8714729985044/100209 - 753347/09-OCT-2020 through 26-MAR-2026; M365DB12320/8714729985051/100104 - 753200/09-OCT-2020 through 21-MAR-2026

Reason for recall

Deep Brain Stimulation (DBS) Implantable Pulse Generator (IPG) may experience routine system check during IPG charging, which may cause device reset. The device reset could lead transient loss of stimulation; patients may experience undesired sensations, transient worsening of movement disorder symptoms, which may lead patient to request surgical intervention for replacement or revision.

Action

On 4/18/24, correction notices were mailed to Physicians/Surgeons, Hospitals, Healthcare Professionals who were asked to do the following: 1) Review any patient reports of undesired sensations indicative of potential device reset behavior during IPG charging and report these observations accordingly to the firm. 2) After firm verifies this device reset behavior has occurred during IPG charging, an in-field IPG firmware update can be scheduled for the patient s device. This will eliminate the possibility of a coincident routine device system check during IPG charging, thus preventing a potential system reset. Any adverse events or quality concerns associated with use of this product should be reported to firm via email BSN.ComplaintCallCenter@bsci.com

Distribution pattern

Worldwide - US Nationwide distribution including in the states of TX, WA, MT, GA, TN, MA, OR, ID, CA, FL, WI, UT, DE, AZ, PA, DC, LA, KY, VA, MN, NC, OH, NY, MI, CO, IN, MD, NV, AL, IL, AR, SC, OK, MO, MS, NJ, ME, Hi, KS, SD, WV, NM, AK, CT, WY, NE, ND and the countries of Canada, Argentina, Chile, Colombia, Brazil, Algeria, Austria, Belgium, Bulgaria, Croatia, Denmark, Finland, France, Germany, Great Britain, Greece, Hungary, Iceland, Ireland, Italy, Jordan, Kazakhstan, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Saudi Arabia, Serbia, Slovakia, Spain, Sweden, Switzerland, Turkey, Ukraine, United Arab Emirates, Australia, Thailand, Singapore, Hong Kong, Korea, India, Japan.

PMA numbers
P150031
Harmonized identifiers (openFDA)
Device name
Stimulator, Electrical, Implanted, For Parkinsonian Symptoms
Medical specialty description
Unknown
Device class
3
PMA number
P150031, P960009
Registration number
3018094310, 3010086866, 2649622, 3015924373, 3006705815, 9616693, 2183744, 3004593495, 2133772, 3005210579, 3003120897, 3003335547, 2182207, 3010052483, 1627487, 3019807891, 3009380063, 3010972758, 1928237, 3013023969, 2133641, 2135338, 3003477135, 2648729, 2124215, 2024311, 3006630150, 3005160949, 3010531069, 3038429246, 3015200795, 3004209178
FEI number
3018094310, 3010086866, 2649622, 3015924373, 3000203466, 3005700659, 3004369318, 3006705815, 2183744, 3004593495, 3000209794, 3005210579, 3003120897, 3003335547, 2182207, 3010052483, 1627487, 3019807891, 3009380063, 3010972758, 3002618605, 1928237, 3013023969, 3003477135, 2648729, 2124215, 2024311, 3006630150, 3005160949, 3010531069, 3038429246, 3015200795
Wholesale access for licensed clinicians.

Free to join: your NPI is checked against the federal registry at signup, then wholesale pricing and the professional shelves open.

Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.