Class II · Moderate riskOngoing Initiated Nov 29, 2021 (5 years ago)
Diclofenac Sodium Topical Solution, 1.5% w/w, packaged in 150 mL bottles, Rx only, Mfg…
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Defective container: Out of specification for container integrity leading to bottles leaking.
What was recalled
Diclofenac Sodium Topical Solution, 1.5% w/w, packaged in 150 mL bottles, Rx only, Mfg: SOLA Pharmaceuticals Preferred Pharmaceuticals, Inc., NDC 68788-7707-01
Recalling firm
Preferred Pharmaceuticals, Inc.
NDC code
68788-7707-01
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0278-2022
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
Reason CGMP Deviations: all products within expiry are being recalled because the manufacturing firm, Teligent Pharma, Inc. is discontinuing its stability…