FDA Class I · Medical device · May 20, 2026
Rolls of label stock used with the Omnicell i recall — Omnicell, Inc.
Potential for mislabeled syringe produced by the i.v.STATION device.
Official ID Z-2047-2026 · Official record ↗
Omnicell recalls
Recall found. Omnicell is named in FDA Class I recall Z-2047-2026 covering Rolls of label stock used with the Omnicell i. Hazard: Potential for mislabeled syringe produced by the i.v.STATION device. Identifying details: 1. Part Number 258920028, Lot Number: QN 200023473. 2. Part Number 258900029, Lot Number: QN 200023474.. Status: Ongoing.
Models with recalls
All Omnicell recalls
Verify with the official sources:
- CPSC — consumer products ↗ (aggregated here)
- NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
- FDA — food, drugs, medical devices ↗ (aggregated here)
- USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
- Recalls.gov — the U.S. government’s all-agency portal ↗
Found something wrong or missing? Report a data error.
Compiled from official public-domain government data. Last checked October 22, 2026 at 6:00 PM UTC.