Reported Mar 30, 2016 · Terminated
Algostim LLC, Algovita Implanted Pulse Generator stimulator, Model 2412 ( 2 x 12 channel)
QiG Group LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: QiG Group LLC · 10675 Naples St NE · Blaine, MN · 55449-5802
Is this the product you have?
- Algostim LLC, Algovita Implanted Pulse Generator stimulator, Model 2412 ( 2 x 12 channel)
- Lot codes and dates
- Serial Numbers
03EDB503EDD903EDDA03EDDB03EDDD03EDE003EDE403EDF503EDF603EDFA03EDFC03EDFF03EE0703EE0803EE0A03EE0D03EE0E03EE1203EE1303EE1A03EE3003EE3C03EE3F03EE4403EE4803EE4C03EE4D03EE6D03EE7403EE8203EE8803EE8903EE8F03EE94
- Serial Numbers
- Amount recalled
- 34
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Why it was recalled
The implantable pulse generator (IPG) model 2408 had suboptimal performance establishing a connection to the external devices unless they were brought into close proximity (as close as 5 cm). The following functions may not be available: Reprogramming the stimulator, Adjusting stimulation parameters (on/off, intensity modifications, stimulation program selection), and Recharging the stimulator.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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