FDA Drug recall D-0807-2017
ADD HEPARIN PF 50 Units ONLY TO TPN all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
- FDA Drug
- Class II
- terminated
- Published 2017-05-31
On 2017-05-31 the FDA classified a Class II recall of ADD HEPARIN PF 50 Units ONLY TO TPN all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054 by Advanced Pharma, citing labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0807-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-02-22 |
| Published | 2017-05-31 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Advanced Pharma |
| Distribution | US |
Product
ADD HEPARIN PF 50 Units ONLY TO TPN all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
Reason
Labeling: Not Elsewhere Classified: Products may contain synthetic latex and/or natural latex.
Identifiers
| code_info | all lots |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0807-2017%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.