Reported Aug 19, 2015 · Terminated

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

Cadence Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Cadence Inc. · 2080 Plainfield Pike · Cranston, RI · 02921-2012

Is this the product you have?

    • Micro-Mate Tuberculin Glass Syringe
    • Non-sterile Catalog numbers 5208
    • 5209
Lot codes and dates
  • Packged LotsCatalog
  • 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
Amount recalled
1665 units

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

  • Nationwide

Why it was recalled

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

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Jul 29, 2016 · Data as of Sep 19, 4:47 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.