Merck Millipore Ltd.
Merck Millipore Ltd. appears in FDA public data with 1 recall, 2 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent recall (Z-0489-2019, Class II) was initiated on May 14, 2018. Its most recent 510(k) clearance was granted on August 11, 2015.
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 2
- Inspections
- 1
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-0489-2019 | Class II | Minicon Clinical Sample Concentrators for In Vitro Diagnostic Use 9031 (Model: Minicon B-15) & 9051 | May 14, 2018 |