FDA Drug recall D-0235-2024
Atropine Sulfate Injection, USP 1 mg/10 mL (0.1 mg/mL), Lifeshield, Glass ABBOJECT Unit of Use Syringe, Rx Only, 10 mL Syringe per Carton,…
- FDA Drug
- Class I
- ongoing
- Published 2024-01-24
On 2024-01-24 the FDA classified a Class I recall of Atropine Sulfate Injection, USP 1 mg/10 mL (0.1 mg/mL), Lifeshield, Glass ABBOJECT Unit of Use Syringe, Rx Only, 10 mL Syringe per Carton,… by Pfizer, citing presence of Particulate Matter; identified as glass.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0235-2024 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2023-12-21 |
| Published | 2024-01-24 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Pfizer |
| Distribution | US |
Product
Atropine Sulfate Injection, USP 1 mg/10 mL (0.1 mg/mL), Lifeshield, Glass ABBOJECT Unit of Use Syringe, Rx Only, 10 mL Syringe per Carton, Hospira, Inc., Lake FOrest, IL 60045, NDC 0409-4911-11 (carton), 0409-4911-34 (case).
Reason
Presence of Particulate Matter; identified as glass
Identifiers
| ndc | 0409-1630-15 |
|---|---|
| ndc | 0409-1630-10 |
| ndc | 0409-9630-15 |
| ndc | 0409-9630-05 |
| ndc | 0409-4910-11 |
| ndc | 0409-4910-34 |
| ndc | 0409-4911-11 |
| ndc | 0409-4911-34 |
| code_info | Lot GY2496, Exp 02/01/2025 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: ongoing.
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Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0235-2024%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.