Atrovent HFA Inhalation Aerosol — Class II drug recall D-1691-2012
Terminated recall by Dispensing Solutions, Inc, reported 2012-10-03, distributed in IN, WI. Label Mix up; side panel of sticker label applied by Dispensing Solutions Inc. incorrectly indicates product n
| Recall number | D-1691-2012 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Dispensing Solutions, Inc, Santa Ana, CA, United States |
| Recall initiated | 2012-08-28 |
| Classified | 2012-09-25 |
| Reported by FDA | 2012-10-03 |
| Terminated | 2012-11-01 |
| Distributed | IN, WI |
| Quantity | 18 inhalers |
| Reason classes | labeling |
| NDC | 68258-8952-01 |
| Lot numbers | F22311, F23989 |
Product
Atrovent HFA Inhalation Aerosol, (ipratropium bromide) 12.9 grams, 200 metered actuations, Rx only, Packaged Exclusively by: Dispensing Solutions, Inc., Santa Ana, CA --- NDC 68258-8952-01, DSI product #8A0947
Reason for recall
Label Mix up; side panel of sticker label applied by Dispensing Solutions Inc. incorrectly indicates product name as Ventolin HFA 90 mcg instead of correctly as Atrovent HFA 12.9 grams Inhalation Aerosol
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-1691-2012. 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.