SpineFrontier, Inc.: 32 recalls on record
Recalls filed with 1 agency: FDA (32).
First recall on record: November 28, 2012. Most recent: July 24, 2019.
Risk classification: Class II: 32
Most recent recalls
| Date | Agency | Product | Recall number |
|---|---|---|---|
| July 24, 2013 | FDA | KRD1 PedFuse Rods, Model: IM80100-13 Rev B Product Usage: Pedicle rods are cylindric…Z-1737-2013 | Z-1737-2013 |
| July 10, 2013 | FDA | S-LIFT Inserter Outer Sleeve Product Usage: The Inserter Sleeve is an optional instr…Z-1665-2013 | Z-1665-2013 |
| July 10, 2013 | FDA | InSpan Inserter, Right Assembly; InSpan Inserter, Left Assembly Product Usage: Insert…Z-1666-2013 | Z-1666-2013 |
| July 10, 2013 | FDA | BASE, S-LIFT Instrument Case Product Usage: System cases are designed to hold and se…Z-1664-2013 | Z-1664-2013 |
| June 12, 2013 | FDA | Straight Impactor - Dorado IBC, Part Number: SI02140. The device is used to position impl…Z-1482-2013 | Z-1482-2013 |
| November 28, 2012 | FDA | S-Lift Implant Guides (also known as S-LIF) Compressor Part Number: 11-50223 Produc…Z-0417-2013 | Z-0417-2013 |
| November 28, 2012 | FDA | Spine Frontier Inspan compressors Part Number: 11-60004. Inspan compressors provide p…Z-0412-2013 | Z-0412-2013 |
Questions about this company
- How many recalls does SpineFrontier, Inc. have?
- Recalert has 32 U.S. recalls on record for SpineFrontier, Inc., published between November 28, 2012 and July 24, 2019.
- Which agencies have handled SpineFrontier, Inc. recalls?
- SpineFrontier, Inc. appears as the recalling firm in recalls from: FDA (32).
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