Mayne Pharma Inc recalls

6 recalls on record · latest: June 9, 2022

Official U.S. recall history for Mayne Pharma Inc, compiled from official government records.

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Mayne Pharma Inc recalls Clonidine Transdermal System, USP 0.3 mg/day, 4 Patches (NDC 51862-455-01) per Carton (51862-455-04), Rx only, Manufact…

June 9, 2022 · Drug & medication recalls Moderate risk Defective Delivery System: Out of specification for release liner removal force…

Lexette Topical Foam recalled over manufacturing violations

January 14, 2022 · Drug & medication recalls Moderate risk CGMP Deviation: Difficulty dispensing/does not dispense or dispensing liquid in…

Mayne Pharma Inc recalls Carbidopa and Levodopa Tablets, USP 25 mg/250mg, 100 ct bottle, Rx Only, Mayne Pharma, Greenville, NC 27834. NDC 51862-…

March 2, 2020 · Drug & medication recalls Moderate risk Product Mix-Up: A foreign tablet was found in bottle.

Oxycodone and Acetaminophen Tablets recalled over labeling errors

August 21, 2018 · Drug & medication recalls Labeling: Incorrect or Missing Lot and/or Exp Date: Lot FG10517 is mislabeled o…

Mayne Pharma Inc recalls Fabior (tazarotene) Foam, 0.1%, 100 grams can, Rx only, Distributed by: Mayne Pharma, Greenville, NC 27834; NDC 51862-2…

March 21, 2018 · Drug & medication recalls Superpotent Drug: High out of specification results for tazarotene assay at the…

Mayne Pharma Inc recalls Liothyronine Sodium Tablets, USP 25 mcg ,100-count bottles, Rx Only, Distributed by Perrigo Minneapolis, MN 55427, NDC…

November 9, 2017 · Drug & medication recalls Moderate risk Failed Dissolution Specifications.