Cadence Inc.: Medical Device Recall in 2015 - (Recall #: Z-2364-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

Perfectum Tuberculin Glass Syringe, Non sterile Catalog numbers 5202, 5205, 5212

Product Classification:

Class II

Date Initiated: July 9, 2015

Date Posted: August 19, 2015

Recall Number: Z-2364-2015

Event ID: 71674

Reason for Recall:

Graduation marks of the syringe are not centered with the numeric position marks on the syringe barrel.

Status: Terminated

Product Quantity: 766 units

Code Information:

Packged Lots: Catalog Number 5202: 79713-04, 80468-05, W003542/1, W006324/1, W006324/2, W006324/3, W006324/4, W006324/5; Catalog Number 5205: 79748-03; Catalog Number 5212: W008136/1, W008686/1, W011240/1, W010905/1, W012135/1, W014053/1, W015838/1, W011240

Distribution Pattern:

Nationwide Foreign Canada, Denmark. Italy

Voluntary or Mandated:

Voluntary: Firm initiated