Cadence Inc.: Medical Device Recall in 2015 - (Recall #: Z-2365-2015)

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:

Micro-Mate Tuberculin Glass Syringe, Non-sterile Catalog numbers 5208, 5209

Product Classification:

Class II

Date Initiated: July 9, 2015

Date Posted: August 19, 2015

Recall Number: Z-2365-2015

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: 1665 units

Code Information:

Packged Lots: Catalog Number 5208: 79895-01, 80044-02, 82350-01, W006510/1; Catalog Number 5209: 71880-01, 76434-01, 76461-01, 76461-02, 76461-03, 76461-04, 76461-05, 76461-06, 76461-07, 76461-08, 79748-01, 80044-03, W001711/1, W002337/1, W002886/1

Distribution Pattern:

Nationwide Foreign Canada, Denmark. Italy

Voluntary or Mandated:

Voluntary: Firm initiated