Eli Lilly & Company recalls
Every recall we track for Eli Lilly & Company — 4 in all, from 2021–2024 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Eli Lilly & Company peaked in 2021 (3); 4 since 2017.
All FDA recall records for Eli Lilly & Company 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 | 2 | 1 | 3 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 1 | 1 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Eli Lilly & Company 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 Eli Lilly & Company recalls
4 shown- UnratedDrug
Eli Lilly & Company recalls Sterile Diluent, HUMALOG U-100 (insulin lispro injection), HUMULIN R U-100 REGULAR (insulin human injection), Insulin
Eli Lilly recalls specific insulin products due to manufacturing deviations. Affected products include Humalog U-100 and Humulin R U-100 Regular. Consumers should check product labels for batch numbers and NDC codes.
Eli LillyMar 12, 2024 - UnratedDrug
Eli Lilly & Company recalls Glucagon Emergency Kit for Low Blood Sugar, Glucagon for Injection, 1 mg per vial; Diluent for Glucagon, 1 mL syringe.
Eli Lilly recalls Glucagon Emergency Kits for low blood sugar due to subpotent drug content. The vial contains liquid instead of powder, reducing effectiveness. No remedy specified in official notice.
Eli LillySep 24, 2021 - Lower riskDrug
Eli Lilly & Company recalls Trulicity (dulaglutide), 0.75 mg/0.5 mL, 4 Single-Dose Pens per box, Rx only, Eli Lilly and Company, Indianapolis, IN
Eli Lilly recalls Trulicity pens labeled 0.75mg but containing 1.5mg due to labeling error. Patients may receive higher dose than intended.
Eli LillyAug 19, 2021 - Lower riskDrug
Eli Lilly & Company recalls Zyprexa Intramuscular, Olanzapine for Injection, 10 MG per Single Use Vial, Rx only, Marketed by: Lilly USA, LLC,
Lilly recalls Zyprexa 10mg injection vials due to cGMP deviations affecting drug appearance, size, and color. Affected vials may have safety concerns.
LillyJun 29, 2021
Eli Lilly & Company recall questions
How many recalls has Eli Lilly & Company had?
4 recalls from Eli Lilly & Company are on record with U.S. safety agencies, from 2021–2024.
What is the most recent Eli Lilly & Company recall?
Eli Lilly & Company recalls Sterile Diluent, HUMALOG U-100 (insulin lispro injection), HUMULIN R U-100 REGULAR (insulin human injection), Insulin, dated Mar 12, 2024. Every Eli Lilly & Company recall is listed on this page, newest first.
What should I do if I have a recalled Eli Lilly & Company 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 Eli Lilly & Company 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.