FDA Device recall Z-0270-2020
SCFE (slipped capital femoral epiphysis) Knobs for Driver, 6.5mm and 7.3 mm Orthopedic surgical instrument component, for hip surgery
- FDA Device
- Class II
- terminated
- Published 2019-11-13
On 2019-11-13 the FDA classified a Class II recall of SCFE (slipped capital femoral epiphysis) Knobs for Driver, 6.5mm and 7.3 mm Orthopedic surgical instrument component, for hip surgery by Pega Medical, citing there is a potential for the screws to have become loosened during ultrasonic cleaning of the knobs and the screws may come out.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0270-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-10-02 |
| Published | 2019-11-13 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Pega Medical |
| Distribution | US |
Product
SCFE (slipped capital femoral epiphysis) Knobs for Driver, 6.5mm and 7.3 mm Orthopedic surgical instrument component, for hip surgery
Reason
There is a potential for the screws to have become loosened during ultrasonic cleaning of the knobs and the screws may come out.
Identifiers
| code_info | Catalogue Numbers: SCF-KNB265, SCF-KNB273, SCF-KNB365, SCF-KNB373; Lot Numbers: 160428-03, 160428-04, A182-05, A182-15, 160603-05, 160603-06, A183-06 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0270-2020%22
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