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 ↗
1 recent recall on record for Omnicell in CPSC, NHTSA, and FDA data as of July 24, 2026 at 3:00 AM UTC.
Potential for mislabeled syringe produced by the i.v.STATION device.
Official ID Z-2047-2026 · Official record ↗
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Compiled from official public-domain government data. Last checked July 24, 2026 at 3:00 AM UTC.