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.
- 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.