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Greiner Bio-One North America, Inc. recalls

Every recall we track for Greiner Bio-One North America, Inc. — 12 in all, from 2019–2025 — plus the complaints and injury reports the public filed about them.

12recalls

Recalls per year, by danger level

Recalls from Greiner Bio-One North America, Inc. peaked in 2021 (4); 12 since 2017.

2017: 0 recalls20172018: 0 recalls20182019: 1 recall — 1 lower risk120192020: 2 recalls — 2 lower risk220202021: 4 recalls — 4 lower risk420212022: 0 recalls20222023: 2 recalls — 1 use caution, 1 lower risk220232024: 1 recall — 1 lower risk120242025: 2 recalls — 2 lower risk220252026 (to date): 0 recalls2026to date

All FDA recall records for Greiner Bio-One North America, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.

Recalls per year for Greiner Bio-One North America, Inc., by danger level
YearStop using nowUse cautionLower riskNot yet ratedTotal
201700000
201800000
201900101
202000202
202100404
202200000
202301102
202400101
202500202
2026 (to date)00000

What to do if you have a recalled Greiner Bio-One North America, Inc. product

  1. Match the model, catalog or lot number on your device to the recall.
  2. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
  3. Report problems to FDA MedWatch.

See this week’s new recalls.

All Greiner Bio-One North America, Inc. recalls

12 shown

Greiner Bio-One North America, Inc. recall questions

How many recalls has Greiner Bio-One North America, Inc. had?

12 recalls from Greiner Bio-One North America, Inc. are on record with U.S. safety agencies, from 2019–2025.

What is the most recent Greiner Bio-One North America, Inc. recall?

Greiner Bio-One North America, Inc. recalls Brand Name: Vacuette Product Name: 8 ml CAT Serum Separator Clot Activator Model/Catalog Number: 455071P Product, dated Aug 19, 2025. Every Greiner Bio-One North America, Inc. recall is listed on this page, newest first.

What should I do if I have a recalled Greiner Bio-One North America, Inc. product?

Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.

How do I get alerts for new Greiner Bio-One North America, Inc. recalls?

Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.