McKesson recalls
Every recall we track for McKesson — 4 in all, from 2014–2026 — 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 McKesson 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 | 1 | 1 |
| 2026 (to date) | 0 | 0 | 2 | 0 | 2 |
McKesson recalls before 2017
Recalls on record by year.
What to do if you have a recalled McKesson 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 McKesson recalls
4 shown- Lower riskDrug
McKesson recalls Gemcitabine Injection, 1 g per 26.3 mL (38 mg/mL), 26.3 mL Single-Dose Vial, For Intravenous Infusion ONLY, Rx only,
McKesson recalls Gemcitabine injection vials stored at room temperature instead of refrigerated. This could affect cancer treatment safety. Check your NDC 0143-9341-01 lot CB0046 for affected units.
McKessonJun 10, 2026 - Lower riskDrug
McKesson recalls UDENYCA, pegfilgrastim-cbqv injection, 6 mg/0.6mL Single Dose Prefilled Syringe, Rx only, Manufactured by Accord
McKesson recalls specific UDENYCA injections (6 mg/0.6mL) manufactured by Accord BioPharma that were stored incorrectly in non-refrigerated conditions. This may affect product safety.
McKessonJan 16, 2026 - UnratedDrug
McKesson recalls Inflectra (infliximab-dyyb), For injection, 100mg per vial, packaged in 10 mL single-dose vial, Rx only, Mfd by:
McKesson recalls Inflectra (infliximab-dyyb) 100mg vials due to cGMP deviations where product intended for quarantine was distributed. This affects specific lots and requires immediate action.
McKessonJan 17, 2025 - Use cautionDrug
Mckesson recalls Amiodarone HCl Injection, 450 mg/9 mL (50 mg per mL), 9 mL Single-Use Vial, Rx only, Manufactured for Mylan
McKesson recalls Mylan Amiodarone HCl Injection vials stored at wrong temps. Check lot #140502, exp 10/31/2015 for potential potency issues.
MylanSep 12, 2014
McKesson recall questions
How many recalls has McKesson had?
4 recalls from McKesson are on record with U.S. safety agencies, from 2014–2026.
What is the most recent McKesson recall?
McKesson recalls Gemcitabine Injection, 1 g per 26.3 mL (38 mg/mL), 26.3 mL Single-Dose Vial, For Intravenous Infusion ONLY, Rx only,, dated Jun 10, 2026. Every McKesson recall is listed on this page, newest first.
What should I do if I have a recalled McKesson 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 McKesson 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.