BonaDur For Men spray recalled over manufacturing violations
- Recall date
- February 7, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Webrx dba RxPalace.com recalls BonaDur For Men (lidocaine) spray, 10 mg per spray, Net Contents .25 fl. oz. (7.4 mL) spray bottles, Manufactured by We…
- Recall number
- D-0421-2018
- FDA classification
- Class III
- Brand / firm
- Webrx dba RxPalace.com
- Sold / distributed
- NY
Why it was recalled
CGMP Deviations: not manufactured according to current good manufacturing practices.
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
BonaDur For Men (lidocaine) spray, 10 mg per spray, Net Contents .25 fl. oz. (7.4 mL) spray bottles, Manufactured by WebRx Pharmacy Palace, Sarasota, FL 34232; NDC 70582-999-74
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