FDA Drug recall D-0095-2022
Acetaminophen Oral Suspension, 325 mg/10.15 mL, packaged in 10.15 mL per cup (NDC Individual cup: 68094-330-59), in a) 30-count case (NDC 3…
- FDA Drug
- Class II
- terminated
- Published 2021-11-17
On 2021-11-17 the FDA classified a Class II recall of Acetaminophen Oral Suspension, 325 mg/10.15 mL, packaged in 10.15 mL per cup (NDC Individual cup: 68094-330-59), in a) 30-count case (NDC 3… by Precision Dose, citing cGMP Deviations: Product manufactured with contaminated raw ingredient.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0095-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-11-01 |
| Published | 2021-11-17 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Precision Dose |
| Distribution | US |
Product
Acetaminophen Oral Suspension, 325 mg/10.15 mL, packaged in 10.15 mL per cup (NDC Individual cup: 68094-330-59), in a) 30-count case (NDC 30-count case: 68094-330-62), and b) 100-count case (NDC 100-count case: 68094-330-61), Hospital Use Only, Pkg. Precision Dose, Inc., S. Beloit, IL 61080.
Reason
cGMP Deviations: Product manufactured with contaminated raw ingredient.
Identifiers
| ndc | 68094-231-59 |
|---|---|
| ndc | 68094-231-62 |
| ndc | 68094-231-61 |
| ndc | 68094-231-01 |
| ndc | 68094-231-58 |
| ndc | 68094-330-59 |
| ndc | 68094-330-62 |
| ndc | 68094-330-61 |
| ndc | 68094-030-59 |
| ndc | 68094-030-62 |
| code_info | Lot#: 503679, 503693, 503715 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0095-2022%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.