Mayne Pharma Recalls
6 recalls on record · December 6, 2017 to June 29, 2022 · Drugs
Recalls by year
17
18
20
22
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
June 29, 2022DrugsFDA
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, Manufac
Hazard: Defective Delivery System: Out of specification for release liner removal force results at the 3-month CRT stability timepoint.
January 26, 2022DrugsFDA
Mayne Pharma Inc recalls Lexette (halobetasol propionate) Topical Foam, 0.05% 50 g canisters, Rx ONLY, Distributed by: Mayne Pharma Greenville,
Hazard: CGMP Deviation: Difficulty dispensing/does not dispense or dispensing liquid instead of foam.
March 18, 2020DrugsFDA
Mayne Pharma Inc recalls Carbidopa and Levodopa Tablets, USP 25 mg/250mg, 100 ct bottle, Rx Only, Mayne Pharma, Greenville, NC 27834. NDC 51862-8
Hazard: Product Mix-Up: A foreign tablet was found in bottle.
September 5, 2018DrugsFDA
Mayne Pharma Inc recalls Oxycodone and Acetaminophen Tablets, USP, 5 mg*/325 mg, 100-count bottle, Rx Only, Manufactured by: Mayne Pharma, Greenv
Hazard: Labeling: Incorrect or Missing Lot and/or Exp Date: Lot FG10517 is mislabeled on the primary container with Lot FG01517, shipper labels and invoices contain the correct lot number of FG10517.
April 11, 2018DrugsFDA
Mayne Pharma Inc recalls Fabior (tazarotene) Foam, 0.1%, 100 grams can, Rx only, Distributed by: Mayne Pharma, Greenville, NC 27834; NDC 51862-29
Hazard: Superpotent Drug: High out of specification results for tazarotene assay at the 9-month stability time point.
December 6, 2017DrugsFDA
Mayne Pharma Inc recalls Liothyronine Sodium Tablets, USP 25 mcg ,100-count bottles, Rx Only, Distributed by Perrigo Minneapolis, MN 55427, NDC
Hazard: Failed Dissolution Specifications.