Proparacaine Hydrochloride Ophthalmic Solution — Class II drug recall D-0661-2024
Terminated recall by Mckesson Medical-Surgical Inc. Corporate Office, reported 2024-10-02, distributed in MD, VA. Temperature abuse: Products exposed to improper temperature above drug label specifications.
| Recall number | D-0661-2024 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Mckesson Medical-Surgical Inc. Corporate Office, Richmond, VA, United States |
| Recall initiated | 2024-09-11 |
| Classified | 2024-09-20 |
| Reported by FDA | 2024-10-02 |
| Terminated | 2025-01-29 |
| Distributed | MD, VA |
| Quantity | 27 bottles |
| Reason classes | labeling, temperature control |
| NDC | 24208-0730, 24208-0730-06 |
| Lot numbers | 476261, 479741, 479751 |
| Expiration dates | 2026-03-31 |
Product
Proparacaine Hydrochloride Ophthalmic Solution, USP 0.5% (sterile), 15 mL bottle, Rx only, MFG: Bausch & Lomb, NDC 24208-730-06
Reason for recall
Temperature abuse: Products exposed to improper temperature above drug label specifications.
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-0661-2024. 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.