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FDA (Device enforcement)Recalled 2020-03-12closedclass ii

Greiner Bio-One North America, Inc.: VACUETTE Tube 2ml 9NC Coagulation Sodium Citrate 3.2%. Item no. 454322. Lot no. B1908355.

Is my product affected?

VACUETTE Tube 2ml 9NC Coagulation Sodium Citrate 3.2%. Item no. 454322. Lot no. B1908355.

  • UPC 29120017574488

Check against the official notice below — it lists the full affected range.

What happened

Greiner Bio-One North America, Inc. is recalling VACUETTE Tube 2ml 9NC Coagulation Sodium Citrate 3.2% tubes (Item no. 454322, Lot no. B1908355) due to inconsistent amounts of sodium citrate in the affected lot. Approximately 1,000,800 units were distributed nationwide across 23 states and Puerto Rico.

The source document does not specify a remedy or what affected consumers should do.

Written by software from the official notice below. Not reviewed by a lawyer.

Hazard

Concerned lot of VACETTE 2mL 9NC Coagulation Tubes were shown to have inconsistent amounts of the 2.3% sodium citrate.

Details from the source

Reason for recall: Concerned lot of VACETTE 2mL 9NC Coagulation Tubes were shown to have inconsistent amounts of the 2.3% sodium citrate. Distribution: US nationwide distribution in the states of: NJ, IN, TN, MI, NC, WA, KS, CA, LA, IL, MD, NY, OH, TX, GA, KY, PA, CO, MA, PR, FL, AR, OK and NE. Quantity: 1,000,800 units. Lot/code info: Item no. 454322. Lot no. B1908355. DI no. (01)29120017574488 (17) 200809 (10)B1908355.

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.

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