Lid O Creme Topical Analgesic Cream recalled over manufacturing violations
- Recall date
- June 21, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Pharma-Natural Inc. recalls Lid O Creme (Lidocaine HCL 4% and Menthol 1%) Topical Analgesic Cream, 2.5 Oz (71 g) roll on bottle, Manufactured & Dis…
- Recall number
- D-1502-2019
- FDA classification
- Class II
- Brand / firm
- Pharma-Natural Inc.
- Sold / distributed
- Consignees in FL and TX who may have further distributed Nationwide in the USA and Puerto Rico.
Why it was recalled
CGMP Deviations: products were manufactured with lack of process validation, cleaning validation, stability studies, and other current good manufacturing practice violations.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Lid O Creme (Lidocaine HCL 4% and Menthol 1%) Topical Analgesic Cream, 2.5 Oz (71 g) roll on bottle, Manufactured & Distributed by: Pharma Natural, Inc. Hialeah, FL 33016, NDC 63788-111-25.
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