Class II U.S. Food and Drug Administration

TerSera Therapeutics LLC Zoladex implant, 3.6 mg recall: Temperature Abuse: Product sat in a non-temperature-controlled FedEx trailer

Recall published 18 days ago

Temperature Abuse: Product sat in a non-temperature-controlled FedEx trailer at ambient outdoor conditions for 25.5 hours.

The hazard: Temperature control failure

This product spent time outside the temperature range it needs. Cold-chain failures are recalled on principle, because the evidence of growth arrives too late to be useful.

What the notice says: Temperature Abuse: Product sat in a non-temperature-controlled FedEx trailer at ambient outdoor conditions for 25.5 hours.

Why it matters: The product went outside its required temperature range in storage or transport. That does not prove bacteria grew in it, but it removes the control that was supposed to stop them.

Symptoms and when to call a doctor

If you have eaten it, watch for the usual food-poisoning pattern — stomach cramps, nausea, diarrhoea, sometimes fever — and seek care for a high fever, bloody stools, persistent vomiting or signs of dehydration.

This page is general information, not medical advice. If you feel unwell, a clinician who can see you is the only person able to judge your case.

Recall details

Recall number
D-0875-2026
Published
October 7, 2026
Risk level
Class II
Status
Ongoing
Issued by
U.S. Food and Drug Administration
Brand
TerSera Therapeutics LLC
Product type
Prescription & OTC drugs
Units affected
296 cartons
Distribution
Nationwide
Made in
United States
Lot / code info
Lot#: YN0099, Exp 01/31/2028

Products covered by this recall

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.

Check your product

The notice names 10 codes you can read straight off the package. Type the one printed on yours and the list below narrows to it.

Lot or batch code

Usually ink-stamped near the seam, the cap or the bottom of the pack.

  • YN0099
  • Exp 01
  • 31
  • 2028 — 296 cartons

Best-by / use-by date

Printed beside the lot code, not on the price sticker.

  • 01
  • 31
  • 2028 — 296 cartons

NDC number

On the carton and again on the bottle or blister label.

  • 70720-950-36

Model or item number

On the rating label, the box or the instruction sheet.

  • NDC 707

Package size

Match the net weight or the piece count on the front of the pack.

  • 3.6 mg

Codes are lifted verbatim from the FDA — Drug enforcement notice. A code that is missing here may still be covered — the official notice is the complete list.

What to do about Temperature

TerSera Therapeutics LLC — This product spent time outside the temperature range it needs. Cold-chain failures are recalled on principle, because the evidence of growth arrives too late to be useful.

  1. Do not eat it, even if it looks and smells normal — that is exactly what the recall anticipates.
  2. Clean the shelf it sat on if any packaging has leaked.
  3. If you refroze it after it thawed, discard it rather than keeping it for cooking later.
  4. Check your own fridge or freezer temperature while you are at it: 40°F or below for the fridge, 0°F for the freezer.

Getting a refund without the pack

The commonest reason people skip the refund is that they have already thrown the item away. That rarely matters.

  • A photo of the label and lot code is accepted by most grocers, and so is a card statement line showing the purchase.
  • Store credit is often offered first. You can ask for the original payment method instead, and it is normally granted.
  • No photo either? Ask anyway. Grocery chains settle recall refunds at the service desk because disputing them costs more than paying them.
  • For a multi-pack or a case, ask for the full purchase price rather than a per-unit figure — the recall covers what you paid.

Company contact: TerSera Therapeutics LLC — 520 Lake Cook Rd Ste 500, Deerfield, IL, 60015-5633

The official notice

This page summarises a notice published by U.S. Food and Drug Administration. The agency notice is the authoritative version — read it before you act, and treat it as the final word if anything here looks different.

Open the FDA — Drug enforcement record U.S. Food and Drug Administration recalls

Questions people ask about this recall

Why was TerSera Therapeutics LLC prescription & otc drugs recalled?

Temperature Abuse: Product sat in a non-temperature-controlled FedEx trailer at ambient outdoor conditions for 25.5 hours. Temperature Abuse: Product sat in a non-temperature-controlled FedEx trailer at ambient outdoor conditions for 25.5 hours.

How do I know if I have the recalled product?

Match the codes printed on your package against the notice: lot code YN0099, Exp 01, 31; best-by date 01 or 31; model number NDC 707. If the code on your package is not on that list, your unit is outside the recall.

What should I do with it right now?

Do not eat it, even if it looks and smells normal — that is exactly what the recall anticipates.

Can I get my money back?

A photo of the label and lot code is accepted by most grocers, and so is a card statement line showing the purchase.

Where was the recalled product sold?

It was distributed nationwide.

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