FDA Device recall Z-0696-2021
Spinal Rod Cutter, Item number 00392500200
- FDA Device
- Class II
- terminated
- Published 2020-12-30
On 2020-12-30 the FDA classified a Class II recall of Spinal Rod Cutter, Item number 00392500200 by Zimmer Biomet, citing device has the potential for fracture during use.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0696-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-11-20 |
| Published | 2020-12-30 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Zimmer Biomet |
| Distribution | US |
Product
Spinal Rod Cutter, Item number 00392500200. The product is a nonsterile pin cutter - Product Usage: The intended use of this instrument is to be used for cutting orthopedic rods/pins during orthopedic surgeries.
Reason
Device has the potential for fracture during use.
Identifiers
| code_info | All lots |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Other recalls by Zimmer Biomet
- Polaris 5.5 Spinal System and Polaris 5.5/Cypher Spinal System, Thoracolumbosacral pedicle screw system
FDA Device · Class II · 2020-12-23 · Zimmer Biomet - ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 26 mm, Neutral, O.D. Cup with Spacers, 55 mm Item Number: 00-8065-552-…
FDA Device · Class II · 2020-11-11 · Zimmer Biomet - ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 28 mm, Neutral, O.D. Cup with Spacers, 51 mm Item Number: 00-8065-548-…
FDA Device · Class II · 2020-11-11 · Zimmer Biomet - ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 32 mm, 10 degree inclined face, O.D. Cup with Spacers, 61 mm Number: 0…
FDA Device · Class II · 2020-11-11 · Zimmer Biomet - ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene, I.D. 22 mm, 10 degree inclined face, O.D. Cup with Spacers, 51 mm Number: 0…
FDA Device · Class II · 2020-11-11 · Zimmer Biomet
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0696-2021%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.