Advanced Neuromodulation Systems Inc.: 5 recalls on record
Recalls filed with 1 agency: FDA (5).
First recall on record: July 18, 2012. Most recent: March 6, 2013.
Risk classification: Class II: 5
Most recent recalls
| Date | Agency | Product | Recall number |
|---|---|---|---|
| March 6, 2013 | FDA | Advanced Neuromodulation Systems, Brio DBS System implantable neurostimulator, IPG or R-I…Z-0894-2013 | Z-0894-2013 |
| October 17, 2012 | FDA | The Eon Mini Implantable Pulse Generator (IPG) is a 16-channel, rechargeable, multi-progr…Z-0025-2013 | Z-0025-2013 |
| September 5, 2012 | FDA | Eon (Model 3716) IPG is a dual channel; 8-contact receiver designed to be connected to 4,…Z-2280-2012 | Z-2280-2012 |
| September 5, 2012 | FDA | The Eon Mini Neurostimulation (IPG) System (Model 3788) is a 16-channel, rechargeable, mu…Z-2281-2012 | Z-2281-2012 |
| July 18, 2012 | FDA | Eon Mini Neurostimulation (IPG) System (Model 3788); The product is indicated as an ai…Z-1983-2012 | Z-1983-2012 |
Questions about this company
- How many recalls does Advanced Neuromodulation Systems Inc. have?
- Recalert has 5 U.S. recalls on record for Advanced Neuromodulation Systems Inc., published between July 18, 2012 and March 6, 2013.
- What was the most recent Advanced Neuromodulation Systems Inc. recall?
- FDA recall Z-0894-2013, published March 6, 2013: Advanced Neuromodulation Systems, Brio DBS System implantable neurostimulator, IPG or R-IPG, Model 6788 Implantable Pulse Generator.
- Which agencies have handled Advanced Neuromodulation Systems Inc. recalls?
- Advanced Neuromodulation Systems Inc. appears as the recalling firm in recalls from: FDA (5).
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