Tolmar, Inc. recalls
Every recall we track for Tolmar, Inc. — 4 in all, from 2013–2023 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
3 recalls since 2017.
All FDA recall records for Tolmar, 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 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 1 | 1 |
| 2022 | 0 | 0 | 0 | 1 | 1 |
| 2023 | 0 | 1 | 0 | 0 | 1 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
Tolmar, Inc. recalls before 2017
Recalls on record by year.
What to do if you have a recalled Tolmar, 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 Tolmar, Inc. recalls
4 shown- Use cautionDrug
Tolmar, Inc. recalls Eligard (leuprolide acetate) for injectable suspension, 7.5 mg every month, Sterile, Rx Only, Must be reconstituted
Tolmar recalls Eligard (leuprolide acetate) injections due to higher than expected leuprolide acetate levels in the reconstituted product. This may cause serious side effects. Affected units have NDC 62935-753-75 and lot 13635A1.
TolmarSep 12, 2023 - UnratedDrug
Tolmar, Inc. recalls Naftifine Hydrochloride Gel, USP 1%, packaged in cartons with: a) Net Wt. 90g tube (NDC 0115-1510-48), b) Net Wt. 40g
Tolmar recalls Naftifine Hydrochloride Gel 1% due to failed impurities tests. This prescription gel may contain harmful substances. Consumers should contact the manufacturer for details.
TolmarJul 11, 2022 - UnratedDrug
TOLMAR, Inc. recalls Clindamycin and Benzoyl Peroxide Gel, 1%/5% 25 g jars, Rx only, Mfg by TOLMAR Inc. Fort collins, CO 80526, NDC
Tolmar recalls Clindamycin and Benzoyl Peroxide Gel 1%/5% 25g jars (Rx only) due to superpotent drug risk. Check NDC 0781-7263-68 and lot numbers for affected products.
TolmarNov 8, 2021 - Use cautionDrug
Tolmar, Inc. recalls Ketoconazole Shampoo, 2%, Manufactured by TOLMAR Inc., Fort Collins, CO for Sandoz Inc., Princeton, NJ --- NDC
Sandoz recalls 391,055 bottles of Ketoconazole Shampoo 2% manufactured by Tolmar due to subpotency issues. Check your lot numbers for details.
SandozSep 23, 2013
Tolmar, Inc. recall questions
How many recalls has Tolmar, Inc. had?
4 recalls from Tolmar, Inc. are on record with U.S. safety agencies, from 2013–2023.
What is the most recent Tolmar, Inc. recall?
Tolmar, Inc. recalls Eligard (leuprolide acetate) for injectable suspension, 7.5 mg every month, Sterile, Rx Only, Must be reconstituted, dated Sep 12, 2023. Every Tolmar, Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Tolmar, 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 Tolmar, 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.