VACUETTE TUBE 6 ml K2E K2EDTA 13x100 pink cap-pink ring, non-ridged
Check against the official notice below — it lists the full affected range.
Greiner Bio-One North America, Inc. recalled 962,400 VACUETTE TUBE 6 ml K2E K2EDTA blood collection tubes with pink caps and pink rings (non-ridged) due to a potential clotting issue. The affected tubes include Item Number 456279, Lot B21033DA (expiration 09/08/2022) and Lot B21053R8 (expiration 11/10/2022). These tubes were distributed to Alabama, Arizona, Colorado, Connecticut, Florida, Illinois, Massachusetts, Maryland, Michigan, Missouri, North Carolina, New Mexico, Pennsylvania, Texas, and Virginia, as well as to Canada.
The source document does not specify what action affected consumers should take in response to this recall.
Written by software from the official notice below. Not reviewed by a lawyer.
Blood collection tubes may experience a clotting issue.
Reason for recall: Blood collection tubes may experience a clotting issue. Distribution: Distribution was made to AL, AZ, CO, CT, FL, IL, MA, MD, MI, MO, NC, NM, PA, TX, and VA. Foreign distribution was made to Canada. Quantity: 962,400 tubes Lot/code info: Item Number 456279, Lot B21033DA, exp. 09/08/2022, UDI Case - 39120017571248; UDI Rack - 29120017571241 UPDATE per 9/10/2021 email: Item Number 456279, Lot B21053R8, exp. 11/10/2022, UDI Case -39120017571248; UDI Rack - 29120017571241.
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.