FDA Drug recall D-0588-2020
Hydromorphone HCL in all strengths, all doses and all packaging, AnazaoHealth 5710 Hoover Blvd Tampa, FL 33634
- FDA Drug
- Class II
- terminated
- Published 2019-12-18
On 2019-12-18 the FDA classified a Class II recall of Hydromorphone HCL in all strengths, all doses and all packaging, AnazaoHealth 5710 Hoover Blvd Tampa, FL 33634 by Coast Quality Pharmacy, citing lack of Processing Controls; Environmental sampling revealed 1 CFU (Colony Forming Unit) identified as Talaromyces rotundus, a fungi.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0588-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-09-03 |
| Published | 2019-12-18 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Coast Quality Pharmacy |
| Distribution | US |
Product
Hydromorphone HCL in all strengths, all doses and all packaging, AnazaoHealth 5710 Hoover Blvd Tampa, FL 33634.
Reason
Lack of Processing Controls; Environmental sampling revealed 1 CFU (Colony Forming Unit) identified as Talaromyces rotundus, a fungi.
Identifiers
| code_info | All lots filled 08/26/2019 and dispensed 08/26-29/2019 remaining within expiry. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
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FDA Drug · Class II · 2019-12-18 · Coast Quality Pharmacy
All Coast Quality Pharmacy recalls
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0588-2020%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.