Zoladex implant, 3.6 mg, One single-Use Syringe Recall 2026
ZOLADEXIssued August 31, 2026Updated Reviewed by the Recall Watch editorial team
ZOLADEX 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, En — recalled per FDA on 8/31/2026. Reason: Temperature Abuse: Product sat in a non-temperature-controlled FedEx trailer at ambient outdoor conditions for 25.5 hours..
- Agency
- FDA
- Issued
- Aug 31, 2026
- Brand
- ZOLADEX
- Distribution
- 1 states
- Lots affected
- 2
Steps to take for this recall
Stop using it
Take it out of rotation. Don't consume, wear, or operate.
Verify the match
Compare lot numbers, UPCs, and dates against your product.
Return or dispose
Follow the manufacturer's instructions to refund or safely dispose.
Free case review
Were you or someone in your household prescribed this medication?
- Free
- No obligation
- Licensed attorneys
Attorney advertising.DetailsHide
Recall Watch is not a law firm and does not provide legal or medical advice. Free case reviews are provided by independent licensed attorneys; Recall Watch may receive a referral fee. Prior results do not guarantee a similar outcome. Submitting this form does not create an attorney-client relationship. See our terms and privacy policy.
What's recalled
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.

Restock your medicine cabinet
First-aid kits, thermometers and OTC basics, searched on Amazon.
Need it delivered? Start a free Amazon Prime trial.
Why it was recalled
Temperature Abuse: Product sat in a non-temperature-controlled FedEx trailer at ambient outdoor conditions for 25.5 hours.
Affected products & lot numbers2 lots called out
Affected Lot Numbers
Check your product label — do not use if your lot number appears below.
| Lot Number |
|---|
| Lot#: YN0099 |
| Exp 01/31/2028 |
Where was it sold1 state
USA Nationwide
More recalls like this4 related — by brand, contaminant, and category
Recent Medications recalls
- Wedgewood Pharmacy Certain Compounded Veterinary Medications Within Expiry Recall 20262026
- Par Health Issues Voluntary Nationwide Argatroban Injection Recall 20262026
- Par Pharmaceutical Par Health Issues Voluntary Nationwide Two Lots Recall 20262026
Frequently asked questions
Is the ZOLADEX recall still active?
Yes, this recall is currently active as of August 31, 2026. Do not use or consume the affected product.
What lot numbers are affected?
Affected lot numbers: Lot#: YN0099, Exp 01/31/2028. Check the label on your product.
What should I do if I have the recalled ZOLADEX?
Do not consume or use this product. Return it to the store for a full refund, or dispose of it safely.