Acetaminophen Injection — Class II drug recall D-1348-2022
Terminated recall by Baxter Healthcare Corporation, reported 2022-08-24, distributed nationwide. Temperature Abuse: Product distributed in refrigerated trucks with labels attached to pallets indicating "Refr
| Recall number | D-1348-2022 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2022-08-04 |
| Classified | 2022-08-16 |
| Reported by FDA | 2022-08-24 |
| Terminated | 2024-07-16 |
| Distributed | Nationwide (US) |
| Quantity | 85,680 bags |
| Reason classes | labeling, temperature control |
| NDC | 36000-0306, 36000-0306-60, 36000-0372, 36000-0372-40 |
| Lot numbers | 20K19G64T1, 21K23G65, 21K25G65, 21K26G65, 21K29G67, 21L10G65, 21L13G66, 21L14G66, 21L15G65 |
| Expiration dates | 2022-10-31, 2023-10-31, 2023-11-30 |
Product
Acetaminophen Injection, 10 mg/mL, 1,000 mg/100 mL, 100 mL VIAFLO container bag, Single Dose Container, For Intravenous Use Only, Rx Only, Baxter Healthcare Corporation, Deerfield, IL 60015 USA; NDC 36000-306-60
Reason for recall
Temperature Abuse: Product distributed in refrigerated trucks with labels attached to pallets indicating "Refrigerate Upon Arrival", however product is labeled to be stored in a controlled room temperature environment.
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-1348-2022. 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.