Biomet Spine, LLC: 5 recalls on record
Recalls filed with 1 agency: FDA (5).
First recall on record: November 26, 2014. Most recent: November 11, 2015.
Risk classification: Class II: 5
Most recent recalls
| Date | Agency | Product | Recall number |
|---|---|---|---|
| November 11, 2015 | FDA | MaxAn 4.0mm and 4.5mm fixed screws, used in the MaxAn Anterior Cervical Plate System. The…Z-0203-2016 | Z-0203-2016 |
| September 16, 2015 | FDA | Biomet Parsippany, NJ. 4 0 MM X 14 MM Variable Screw C-Tek Maxan Anterior Cervical Plate …Z-2744-2015 | Z-2744-2015 |
| April 29, 2015 | FDA | Torque Limiting Handle (Aspen/ Alpine) Model Number 6200-1109 Product Usage: Provid…Z-1466-2015 | Z-1466-2015 |
| January 21, 2015 | FDA | Timberline Anchored Lateral Fixed Retractable Sleeve Model No. 8630-0205. Timberline Anc…Z-0983-2015 | Z-0983-2015 |
| November 26, 2014 | FDA | LANX, REF, PCR8XXX-XXX, LOT, RXONLY. Packaged within aluminum sterilization case. Pro…Z-0220-2015 | Z-0220-2015 |
Questions about this company
- How many recalls does Biomet Spine, LLC have?
- Recalert has 5 U.S. recalls on record for Biomet Spine, LLC, published between November 26, 2014 and November 11, 2015.
- What was the most recent Biomet Spine, LLC recall?
- FDA recall Z-0203-2016, published November 11, 2015: MaxAn 4.0mm and 4.5mm fixed screws, used in the MaxAn Anterior Cervical Plate System. The MaxAn Anterior Cervical Plate System is a decompression-based technique for cervical spine stabilization.
- Which agencies have handled Biomet Spine, LLC recalls?
- Biomet Spine, LLC appears as the recalling firm in recalls from: FDA (5).
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