Pseudoephedrine Oral Solution recalled over manufacturing violations
- Recall date
- May 21, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Torrent Pharma Inc recalls Pseudoephedrine Oral Solution, 30 mg in each teaspoonful, Nasal Decongestant, One Pint (473 mL) bottle, NDC: 0536-1850-…
- Recall number
- D-1353-2019
- FDA classification
- Class II
- Brand / firm
- Torrent Pharma Inc
- Sold / distributed
- Product was distributed to 9 distributors, direct accounts and relabelers who may have further distributed the product throughout the United States.
Why it was recalled
cGMP Deviations: Potential product contamination with Burkholderia cepacia (B.cepacia) and Ralstonia pickettii (R. pickettii).
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Pseudoephedrine Oral Solution, 30 mg in each teaspoonful, Nasal Decongestant, One Pint (473 mL) bottle, NDC: 0536-1850-85, Distributed by Rugby Laboratories, Livonia MI 48152.
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