United Pacific Co Ltd
United Pacific Co Ltd appears in FDA public data with 1 recall, 5 510(k) clearances, 4 FDA inspections, and 0 compliance actions on record. Its most recent recall (D-0624-2018, Class II) was initiated on March 29, 2018. Its most recent 510(k) clearance was granted on October 19, 2000.
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 5
- Inspections
- 4
- Compliance Actions
- 0
Known Names
united pacific co, united pacific
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| D-0624-2018 | Class II | Zhong Hua Jiu (menthol 1%) Patch, Distributed by United Pacific Company, UPC 6 924938 100226, NDC 53 | March 29, 2018 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K003010 | SPIRIT ACUPUNCTURE NEEDLE | October 19, 2000 |
| K001718 | MILLENNIA ACUPUNCTURE NEEDLE | June 21, 2000 |
| K993123 | QK-WIDE BAND SPECTRUM THERAPEUTIC APPARATUS, MODELS CO1A, CO1B, CO1C, CO1D, CO2A, CO2B | December 17, 1999 |
| K991503 | SACRED CRANE TDP LAMP, MODELS CQ-27, CQ-12, CQ-36 | July 28, 1999 |
| K990406 | KINGLI ACUPUNCTURE NEEDLE | April 16, 1999 |