FDA Device recall Z-1935-2012
Vacuette Quickshield Complete Plus, 21G x 1 (0.8 x 25 mm), Greiner bio-one
- FDA Device
- Class II
- terminated
- Published 2012-07-11
On 2012-07-11 the FDA classified a Class II recall of Vacuette Quickshield Complete Plus, 21G x 1 (0.8 x 25 mm), Greiner bio-one by Greiner Bio One North America, citing : The Quickshield Complete Plus may have a defect (split at the base), which can cause the green safety shield attachment of the Quickshield holder to be loose and unstable.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1935-2012 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-04-02 |
| Published | 2012-07-11 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Greiner Bio One North America |
| Distribution | US |
Product
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.
Reason
: The Quickshield Complete Plus may have a defect (split at the base), which can cause the green safety shield attachment of the Quickshield holder to be loose and unstable.
Identifiers
| code_info | Item #450239, Lot #G110601I and Item #450235, Lot #G110302J. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1935-2012%22
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