C. O. Truxton
C. O. Truxton appears in FDA public data with 7 recalls — including 2 Class I (most serious) —, 0 510(k) clearances, 2 FDA inspections, and 1 compliance action on record. Its most recent recall (D-1116-2017, Class II) was initiated on April 20, 2017.
Summary
- Total Recalls
- 7 (2 Class I)
- 510(k) Clearances
- 0
- Inspections
- 2
- Compliance Actions
- 1
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| D-1116-2017 | Class II | Phenobarbital Tablets USP, 15 mg, 1000 count bottles, Rx Only, Manufactured by West-ward Pharmaceuti | April 20, 2017 |
| D-1111-2017 | Class I | Phenobarbital Tablets USP, 15 mg, 1000 count bottles, Rx Only, Manufactured by West-ward Pharmaceuti | April 20, 2017 |
| D-1114-2017 | Class II | Phenobarbital Tablets USP, 100 mg, a) 100 count bottles (NDC 0463-6152-01), b) 1000 count bottles (N | April 20, 2017 |
| D-1112-2017 | Class I | Phenobarbital Tablets USP, 30 mg, 1000 count bottles, Rx Only, Manufactured by West-ward Pharmaceuti | April 20, 2017 |
| D-1113-2017 | Class II | Phenobarbital Tablets USP, 60 mg, 1000 count bottles, Rx Only, Manufactured by West-ward Pharmaceuti | April 20, 2017 |
| D-1115-2017 | Class II | Amitriptyline HCL Tablets, USP 50 mg, 100 count bottles, Rx Only, Manufactured for: Qualitest Pharm | April 20, 2017 |
| D-0164-2016 | Class II | Doxycycline Hyclate Tablets, USP, 100 mg, 500-count bottle, Rx only, Distributed by: Truxton Inc. Be | August 24, 2015 |