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, England, Product of Switzerland, website at www.zoladex.com, NDC 70720-950-36.
Published October 7, 2026 · Recall initiated: August 31, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Temperature Abuse: Product sat in a non-temperature-controlled FedEx trailer at ambient outdoor conditions for 25.5 hours.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- ZOLADEX
- Manufacturer
- TerSera Therapeutics LLC
- Distributor
- USA Nationwide
- Lot
- Lot#: YN0099, Exp 01/31/2028
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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Questions about this recall
Was 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, England, Product of Switzerland, website at www.zoladex.com, NDC 70720-950-36. recalled?
Yes. FDA published recall D-0875-2026 on October 7, 2026. Reported hazard: Temperature Abuse: Product sat in a non-temperature-controlled FedEx trailer at ambient outdoor conditions for 25.5 hours.
What should I do if I have this product?
Voluntary: Firm initiated · Letter
How do I know if my unit is part of the recall?
Compare your product details with the notice. Brand: ZOLADEX.
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