Pega Medical Inc.: Medical Device Recall in 2019 - (Recall #: Z-0270-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

SCFE (slipped capital femoral epiphysis) Knobs for Driver, 6.5mm and 7.3 mm Orthopedic surgical instrument component, for hip surgery

Product Classification:

Class II

Date Initiated: October 2, 2019

Date Posted: November 13, 2019

Recall Number: Z-0270-2020

Event ID: 84017

Reason for Recall:

There is a potential for the screws to have become loosened during ultrasonic cleaning of the knobs and the screws may come out.

Status: Terminated

Product Quantity: 31 devices

Code Information:

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

Distribution Pattern:

Nationwide distribution to CA, FL, GA, HI, LA, MA, MO, NC, NY, OK. International distribution to AUSTRALIA, CANADA, DENMARK, GERMANY, ISRAEL, MEXICO, ROMANIA, RUSSIA, UNITED ARAB EMIRATES, UNITED KINGDOM

Voluntary or Mandated:

Voluntary: Firm initiated