Shilpa Medicare Limited recalls
Every recall we track for Shilpa Medicare Limited — 8 in all, from 2020–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Shilpa Medicare Limited peaked in 2020 (6); 8 since 2017.
All FDA recall records for Shilpa Medicare Limited 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 | 6 | 6 |
| 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 | 2 | 0 | 2 |
Most common reasons for Shilpa Medicare Limited recalls
What to do if you have a recalled Shilpa Medicare Limited 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 Shilpa Medicare Limited recalls
2 shown- Lower riskDrug
Shilpa Medicare Limited recalls PEMRYDI RTU(pemetrexed injection), 500 mg/50 mL (10 mg/mL), Single-dose vial, Rx only, Manufactured by: Zydus
Shilpa Medicare recalls PEMRYDI RTU (pemetrexed injection) due to green discoloration in vials. This may indicate contamination. Check vial color before use.
Shilpa MedicareJul 29, 2026 - UnratedDrug
Shilpa Medicare Limited recalls Azacitidine for Injection 100 mg/vial, For Subcutaneous and Intravenous Use Only, Rx Only, One Single Dose Vial,
Shilpa Medicare Limited recalls Azacitidine 100 mg/vial injections due to CGMP deviations. Affected lots expired by 2022. Contact for return instructions.
Shilpa MedicareDec 8, 2020
Shilpa Medicare Limited recall questions
How many recalls has Shilpa Medicare Limited had?
8 recalls from Shilpa Medicare Limited are on record with U.S. safety agencies, from 2020–2026.
What is the most recent Shilpa Medicare Limited recall?
Shilpa Medicare Limited recalls PEMRYDI RTU(pemetrexed injection), 500 mg/50 mL (10 mg/mL), Single-dose vial, Rx only, Manufactured by: Zydus, dated Jul 29, 2026. Every Shilpa Medicare Limited recall is listed on this page, newest first.
Why are Shilpa Medicare Limited products recalled?
The most common reasons on record: CGMP Deviations (6).
What should I do if I have a recalled Shilpa Medicare Limited 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 Shilpa Medicare Limited 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.