Reported Jul 24, 2024 · Ongoing

VACUETTE¿ TUBE 8 ml CAT Serum Separator Clot Activator 16x100 red cap-yellow ring, non-ridged

Greiner Bio-One North America, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Greiner Bio-One North America, Inc. · 4238 Capital Dr · Monroe, NC · 28110-7681

Is this the product you have?

  • VACUETTE¿ TUBE 8 ml CAT Serum Separator Clot Activator 16x100 red cap-yellow ring, non-ridged
Lot codes and dates
  • Item Number455071P
  • UDI Case label39120017573068
  • UDI Rack label29120017573061
  • Lot NumberB24013MV
Amount recalled
1,008,000pcs (840 cartons)

Where it was sold

Why it was recalled

The firm received reports that some blood collection tubes have experienced issues with clotting and poor separation due to missing additive. The failure of the device would likely require sample recollection which could result in a delay of treatment.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:32 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.