Progressive Laboratories, Inc
Progressive Laboratories, Inc appears in FDA public data with 4 recalls — including 4 Class I (most serious) —, 0 510(k) clearances, 11 FDA inspections, and 0 compliance actions on record. Its most recent recall (F-0915-2018, Class I) was initiated on February 23, 2018.
Summary
- Total Recalls
- 4 (4 Class I)
- 510(k) Clearances
- 0
- Inspections
- 11
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| F-0915-2018 | Class I | Xenesta Nuvive Womens 90 count packaged in a white plastic bottle with white cap | February 23, 2018 |
| F-0912-2018 | Class I | Testosterzone 180 count bottle packaged in an amber plastic bottle with a black cap | February 23, 2018 |
| F-0913-2018 | Class I | Thyroid Resilience 120 count bottle packaged in an amber plastic bottle with black cap | February 23, 2018 |
| F-0914-2018 | Class I | Xenesta Nuvive Mens 90 count packaged in an white plastic bottle with white cap | February 23, 2018 |