[Recalled] VACUETTE Tube 2ml 9NC Coagulation Sodium Citrate 3.2%. Item no. 454322. Lot no. B1908355. — Concerned lot of VACETTE 2mL 9NC Coagulation Tubes were shown to have inconsist… | FDA 2020-03-12
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | VACUETTE Tube 2ml 9NC Coagulation Sodium Citrate 3.2%. Item no. 454322. Lot no. B1908355. |
|---|---|
| Brand / manufacturer | Greiner Bio-One North America, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1714-2020 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 12 March 2020 |
| EAN / barcode | 29120017574488 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Concerned lot of VACETTE 2mL 9NC Coagulation Tubes were shown to have inconsistent amounts of the 2.3% sodium citrate.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Greiner Bio-One North America, Inc.
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.
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