Mayne Pharma Inc recalls
Every recall we track for Mayne Pharma Inc — 6 in all, from 2017–2022 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
6 recalls since 2017.
All FDA recall records for Mayne Pharma Inc since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 1 | 0 | 0 | 1 |
| 2018 | 0 | 1 | 1 | 0 | 2 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 1 | 0 | 1 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 2 | 0 | 2 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Mayne Pharma Inc product
- Match the NDC and lot number on your bottle or box to the recall.
- Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first.
- Report side effects to FDA MedWatch.
All Mayne Pharma Inc recalls
6 shown- Lower riskDrug
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,
Mayne Pharma recalls Clonidine Transdermal System 0.3 mg/day patches due to defective delivery system that may not release properly after 3 months.
Mayne PharmaJun 9, 2022 - Lower riskDrug
Mayne Pharma Inc recalls Lexette (halobetasol propionate) Topical Foam, 0.05% 50 g canisters, Rx ONLY, Distributed by: Mayne Pharma Greenville,
Mayne Pharma recalls Lexette (halobetasol propionate) 0.05% topical foam canisters due to difficulty dispensing or dispensing liquid instead of foam. This is a CGMP deviation affecting certain lots.
Mayne PharmaJan 14, 2022 - Lower riskDrug
Mayne Pharma Inc recalls Carbidopa and Levodopa Tablets, USP 25 mg/250mg, 100 ct bottle, Rx Only, Mayne Pharma, Greenville, NC 27834. NDC
Mayne Pharma recalls 100-count Carbidopa-Levodopa tablets (25mg/250mg) due to a foreign tablet found in the bottle. This Rx-only medication is for Parkinson's disease treatment.
Mayne PharmaMar 2, 2020 - Lower riskDrug
Mayne Pharma Inc recalls Oxycodone and Acetaminophen Tablets, USP, 5 mg*/325 mg, 100-count bottle, Rx Only, Manufactured by: Mayne Pharma,
Mayne Pharma recalls 100-count oxycodone and acetaminophen tablets due to mislabeled lot numbers on packaging, which could lead to confusion in tracking expiration dates.
Mayne PharmaAug 21, 2018 - Use cautionDrug
Mayne Pharma Inc recalls Fabior (tazarotene) Foam, 0.1%, 100 grams can, Rx only, Distributed by: Mayne Pharma, Greenville, NC 27834; NDC
Mayne Pharma recalls Fabior (tazarotene) foam due to high drug levels that could cause serious injury. This prescription-only product was distributed with specific lot and expiration details.
Mayne PharmaMar 21, 2018 - Use cautionDrug
Mayne Pharma Inc recalls Liothyronine Sodium Tablets, USP 25 mcg ,100-count bottles, Rx Only, Distributed by Perrigo Minneapolis, MN 55427, NDC
Mayne Pharma recalls 11,364 bottles of Liothyronine Sodium Tablets 25 mcg distributed by Perrigo due to failed dissolution specifications.
Mayne PharmaNov 9, 2017
Mayne Pharma Inc recall questions
How many recalls has Mayne Pharma Inc had?
6 recalls from Mayne Pharma Inc are on record with U.S. safety agencies, from 2017–2022.
What is the most recent Mayne Pharma Inc recall?
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,, dated Jun 9, 2022. Every Mayne Pharma Inc recall is listed on this page, newest first.
What should I do if I have a recalled Mayne Pharma Inc product?
Match the NDC and lot number on your bottle or box to the recall. Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first. Report side effects to FDA MedWatch.
How do I get alerts for new Mayne Pharma Inc recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.