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VACUETTE
Greiner Bio-One GmbH · Model 454486 · UDI-DI 29120049200300
10
510(k) clearances
180
Adverse events
3
Recalls
43
Facilities
Description
VACUETTE® TUBE 4 ml Urine CCM 13x75 yellow cap-black ring, Round Base, non-ridged
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-01-08 | Hologic, Inc. | Three lots of Rapid fFN Specimen Collection kit (901164, 901165, and 904850) contain Rapid fFN Specimen Collection Tubes which may be empty, underfilled, or overfilled with extract |
| 2020-07-14 | Thomas Scientific | The firm is replacing all tubes that were manufactured and distributed prior to Enforcement Discretion Approval. |
| 2009-05-07 | Remel, Inc | Incorrect expiration date on the product |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.