Phenylephrine HCl 20 mg added to 0 — Class III drug recall D-0778-2023
Terminated recall by New England Life Care, Inc. dba Advanced Compounding Solutions, reported 2023-06-07, distributed nationwide. Product Mix up; Product was compounded in 250 mL 5% Dextrose instead of 250 mL 0.9% Sodium Chloride
| Recall number | D-0778-2023 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | New England Life Care, Inc. dba Advanced Compounding Solutions, Woburn, MA, United States |
| Recall initiated | 2023-05-22 |
| Classified | 2023-06-01 |
| Reported by FDA | 2023-06-07 |
| Terminated | 2023-07-25 |
| Distributed | Nationwide (US) |
| Quantity | 198 |
| NDC | 71546-0451-25 |
| Lot numbers | 20230323-728BF8 |
| Expiration dates | 2023-08-20 |
Product
Phenylephrine HCl 20 mg added to 0.9% Sodium Chloride 250mL Bag, Rx Only, Compounded by: Advanced Compounding Solutions, 4 Constitution Way Ste L Woburn, Massachusetts 01801-1042 United States, NDC 71546-451-25
Reason for recall
Product Mix up; Product was compounded in 250 mL 5% Dextrose instead of 250 mL 0.9% Sodium Chloride
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-0778-2023. 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.