Sandoz's product recalls
2 official recall notices between Jul 2025 and Sep 2025 were matched to Sandoz and brands it owned at the time, including Sandoz.
Each notice concerns the specific products, sizes and lot codes it names. A recall does not mean that other Sandoz products are affected, and a count of notices is not a measure of safety: one incident can produce a notice for every pack size.
Covers only notices from the U.S. Food and Drug Administration enforcement reports (openFDA), USDA Food Safety and Inspection Service recalls, UK Food Standards Agency food alerts and U.S. Consumer Product Safety Commission recalls that could be matched to Sandoz: the recalling firm must be Sandoz, a parent or a subsidiary, and for a brand the brand name must appear in the product description. Method.
2025 (2)
| Date | Product | Brand | Recalling firm | Reason given | Source |
|---|---|---|---|---|---|
| Cyclophosphamide Injection 500 mg/5 mL (100 mg/mL), Hazardous Drug, Rx Only, Sterile, 5mL Multiple Dose Vial, Manufactured in Austria by Fareva Unterach GmbH… | Sandoz | Sandoz Inc | cGMP deviations: Temperature excursion during transportation. Class II | FDA | |
| Buffered Penicillin G Potassium for Injection, USP 20,000,000 Units (20 million units), For IV use, Sterile, Rx Only, Manufactured in Austria by Sandoz GmbH… | Sandoz | Sandoz Inc | Labeling: Label Mix-Up; Some vials of Cefazolin for Injection, USP 1 gram were incorrectly labeled as penicillin G potassium for… Class I | FDA |
Product descriptions and reasons are shortened from the regulators' own text; the linked notice is the authoritative record. See all matched recalls, or report a wrong match through the corrections page.