Prednisolone Sodium Phosphate Oral Solution — Class II drug recall D-1042-2018
Terminated recall by Morton Grove Pharmaceuticals, Inc., reported 2018-08-15, distributed nationwide. Defective Container: Tamper Evident foil seal not completely intact.
| Recall number | D-1042-2018 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Morton Grove Pharmaceuticals, Inc., Morton Grove, IL, United States |
| Recall initiated | 2018-07-24 |
| Classified | 2018-08-03 |
| Reported by FDA | 2018-08-15 |
| Terminated | 2022-09-09 |
| Distributed | Nationwide (US) |
| Quantity | 38,280 bottles |
| Reason classes | packaging |
| NDC | 60432-0212-08 |
| Lot numbers | US1259 |
Product
Prednisolone Sodium Phosphate Oral Solution, 15 mg/5 mL, 8 fl oz (237 mL) Bottle, Rx only, Manufactured By: Morton Grove Pharmaceuticals, Inc., Morton Grove, IL 60053, NDC 60432-212-08.
Reason for recall
Defective Container: Tamper Evident foil seal not completely intact.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1042-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.