Reported Aug 19, 2015 · Terminated
Perfectum Tuberculin Glass Syringe, Non sterile Catalog numbers 5202, 5205, 5212
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?
Perfectum Tuberculin Glass SyringeNon sterile Catalog numbers 520252055212
- Lot codes and dates
3 of 3 products
Products covered by this recall Model / number Product as published 520279713-04, 80468-05, W003542/1, W006324/1, W006324/2, W006324/3, W006324/4, W006324/5 520579748-03 5212W008136/1, W008686/1, W011240/1, W010905/1, W012135/1, W014053/1, W015838/1, W011240 - Amount recalled
- 766 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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