Oxygen — Class II drug recall D-1002-2019
Terminated recall by Roberts Home Medical LLC, reported 2019-03-20, distributed in DC, MD, VA. CGMP Deviations
| Recall number | D-1002-2019 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Roberts Home Medical LLC, Germantown, MD, United States |
| Recall initiated | 2018-12-19 |
| Classified | 2019-03-14 |
| Reported by FDA | 2019-03-20 |
| Terminated | 2019-05-01 |
| Distributed | DC, MD, VA |
| Quantity | 9 reservoirs |
| Reason classes | cgmp |
| Lot numbers | 01001100318, 01002100318, 01005100518, 01007072518, 01007112118, 01010101918, 01011090518, 01011101918, 01017120518 |
Product
Oxygen, Refrigerated Liquid USP, Rx only, cylinder, a) Roberts Home Medical, Inc. Rockville MD 20855, b) Roberts Home Medical, Inc. Germantown, MD. 20875
Reason for recall
CGMP Deviations
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-1002-2019. 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.