Greenstone Llc recalls
Every recall we track for Greenstone Llc — 7 in all, from 2013–2026 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls per year, by danger level
1 recall since 2017.
All FDA recall records for Greenstone Llc 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 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 1 | 0 | 1 |
Greenstone Llc recalls before 2017
Recalls on record by year.
What to do if you have a recalled Greenstone Llc 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 Greenstone Llc recalls
6 shown- Lower riskDrug
Greenstone Llc recalls methylprednisolone tablets, USP Dosepak, 4 mg, 1 Blister Card per Carton containing 21 Tablets, Rx only, Distributed
Greenstone recalls methylprednisolone tablets due to incorrect dosing information on blister packaging. This may lead to improper medication doses if users follow the foil instructions.
GreenstoneJan 15, 2026 - Stop using nowDrug
Greenstone Llc recalls Venlafaxine HCl Extended-Release Capsules, 150 mg, 90-count Unit of Use bottles, Rx only, Distributed by: Greenstone
Greenstone LLC recalls 16,018 bottles of Venlafaxine HCl 150 mg capsules due to the presence of foreign Tikosyn (dofetilide) capsules.
GreenstoneMar 6, 2014 - Use cautionDrug
Greenstone LLC recalls sertraline HCl tablets, 25 mg, 30 Tablets, Rx only, GREENSTONE BRAND --- Distributed by: Greenstone LLC, Peapack, NJ
Greenstone LLC recalls 585,096 bottles of 25mg sertraline tablets because expiration dates may be incorrect. Check your lot numbers now.
GreenstoneNov 5, 2013 - Use cautionDrug
Greenstone Llc recalls Glipizide XL (glipizide) extended release tablets, 5 mg , 500 count bottles, Rx only, Distributed by: Greenstone Ltd.,
Greenstone LLC recalls specific lots of Glipizide XL extended-release tablets because they failed dissolution specifications, potentially affecting how the drug works.
GreenstoneNov 4, 2013 - Use cautionDrug
Greenstone Llc recalls Nifedipine, extended-release tablets, 90mg 100 count blister pack, Rx only, Distributed by: GREENSTONE LLC, Pespack,
Greenstone LLC recalls 21,600 tablets of Nifedipine 90mg because the expiration date is incorrectly labeled as 48 months instead of 36 months.
GreenstoneNov 1, 2013 - Use cautionDrug
Greenstone Llc recalls Spironolactone tablets, USP 25 mg, Rx only, 500 count bottle, Distributed By: Greenstone LLC, Peapack, NJ 07977, NDC:
Greenstone LLC recalls specific lots of 25 mg Spironolactone tablets distributed nationwide due to manufacturing site changes affecting dissolution profiles.
GreenstoneSep 4, 2013
Greenstone Llc recall questions
How many recalls has Greenstone Llc had?
7 recalls from Greenstone Llc are on record with U.S. safety agencies, from 2013–2026.
What is the most recent Greenstone Llc recall?
Greenstone Llc recalls methylprednisolone tablets, USP Dosepak, 4 mg, 1 Blister Card per Carton containing 21 Tablets, Rx only, Distributed, dated Jan 15, 2026. Every Greenstone Llc recall is listed on this page, newest first.
What should I do if I have a recalled Greenstone Llc 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 Greenstone Llc 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.