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Greiner Bio-One North America, Inc.: Medical Device Recalls in 2012

Updated on March 25, 2026.

According to to data from the FDA, there were 2 medical device recalls made by Greiner Bio-One North America, Inc. in 2012. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.
See this for other years:
2012
2013
2016
2020
2021
2022
2023
2024
2025
  • 3mL 9NC Coagulation Sodium Citrate 3.2%, Item #454334, Greiner Bio-One North America Inc., 4238 Capital Drive, Monroe, NC 28110. Intended Use: Venous blood collection tubes.
  • Vacuette Quickshield Complete Plus, 21G x 1 (0.8 x 25 mm), Greiner bio-one. The Quick shield Complete Plus is intended to be used only with Vacuette Blood collection Tubes as a system in routine venipuncture procedures. They are for single-use only and should only be used by adequately trained healthcare personnel in accordance with instructions for use.
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