Drug recall
Zoladex (goserelin) implant, 3.6 mg, One single-Use Syringe packaged in a carton, Rx only, Manufactured for…
FDA recall event 99795 · Class II · TerSera Therapeutics LLC
Key facts
| Event ID | 99795 |
|---|---|
| Recall numbers | D-0875-2026 |
| Recalling firm | TerSera Therapeutics LLC |
| Product type | Drugs |
| Products | Zoladex (goserelin) implant, 3.6 mg, One single-Use Syringe packaged in a carton, Rx only, Manufactured for: TerSera therapeutics LLC, Deerfield, IL 60015, BY: AstraZeneca UK Limited, Macclesfield… |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Temperature Abuse: Product sat in a non-temperature-controlled FedEx trailer at ambient outdoor conditions for 25.5 hours. |
| Initiation date | Aug 31, 2026 |
| Report date | Oct 7, 2026 |
| City | Deerfield |
| State | IL |
| Country | United States |
| FEI number | 3016527790 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: