Safecor Health, LLC Fluphenazine HCl Elixir, USP, 15 mg per 3 mL, Delivers: 10 mL recall: Failed Stability Specifications
Failed Stability Specifications
The hazard: Potency, impurity or stability failure
An out-of-specification result prompted this notice — potency, an impurity, or stability over the shelf life.
What the notice says: Failed Stability Specifications
Why it matters: The product failed a specification test: it may contain more or less active ingredient than the label states, carry an impurity, or degrade before its expiry date. A sub-potent dose can leave a condition untreated; a super-potent one can cause an overdose.
Symptoms and when to call a doctor
The risk depends entirely on the drug. For a medicine where dose matters closely — a blood thinner, an anti-epileptic, a thyroid or heart medicine, insulin — talk to your prescriber before changing anything. Seek urgent care if you have symptoms that suggest too much drug, or if the condition the medicine controls starts breaking through.
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-0845-2026
- Published
- September 23, 2026
- Risk level
- Class II
- Status
- Ongoing
- Issued by
- U.S. Food and Drug Administration
- Brand
- Safecor Health, LLC
- Product type
- Prescription & OTC drugs
- Units affected
- N/A
- Distribution
- Nationwide
- Made in
- United States
- Lot / code info
- Lot#:26080483; Exp :03/13/2027 Lot#:25310327; Exp :08/12/2026 Lot#:25330414; Exp :08/26/2026 Lot#:25430340; Exp :11/22/2026
Products covered by this recall
Fluphenazine HCl Elixir, USP, 15 mg per 3 mL, Delivers: 10 mL, Oral Elixir, PAI, Alcohol 14% by volume, For Oral Use Only, Rx Only, Pkg by: Safecor Health, Woburn, MA 01801. NDC: 00121-0653-04
Check your product
The notice names 18 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.
- 26080483
- 25310327
- 25330414
- 25430340
Best-by / use-by date
Printed beside the lot code, not on the price sticker.
- 03
- 13
- 2027 Lot
- 08
- 12
- 2026 Lot
- 26
- 11
- 22
- 2026 — N
NDC number
On the carton and again on the bottle or blister label.
- 00121-0653-04
Package size
Match the net weight or the piece count on the front of the pack.
- 15 mg
- 3 mL
- 10 mL
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 Potency
Safecor Health, LLC — An out-of-specification result prompted this notice — potency, an impurity, or stability over the shelf life.
- Check the lot number on your pack against the codes listed above before you do anything else.
- Keep the carton and the leaflet — the lot number is usually printed only on the outer pack.
- Report any change in how the medicine is working to FDA MedWatch, which is where most of these signals originate.
- Do not stop a prescription on your own. For most conditions an uncertain dose is safer than no dose while you get advice.
What the company owes you
A recalled medicine is the manufacturer’s cost to carry, not yours or your pharmacist’s.
- The purchase price or co-pay is refundable, and so is the cost of returning the product if they ask you to ship it.
- Ask the pharmacy to handle the claim where they can — they process recall returns in bulk and it saves you the correspondence.
- Keep the carton, the leaflet and the pharmacy label together until the claim is closed.
- Costs beyond the price of the medicine need to go to the company directly, in writing, with the recall number quoted.
Company contact: Safecor Health, LLC — 317 New Boston St, Woburn, MA, 01801-6231
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 Safecor Health, LLC prescription & otc drugs recalled?
Failed Stability Specifications Failed Stability Specifications
How do I know if I have the recalled product?
Match the codes printed on your package against the notice: lot code 26080483, 25310327, 25330414; best-by date 03 or 13. 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?
Check the lot number on your pack against the codes listed above before you do anything else.
Can I get my money back?
The purchase price or co-pay is refundable, and so is the cost of returning the product if they ask you to ship it.
Where was the recalled product sold?
It was distributed nationwide.
Related recalls
-
Class II · last month
Safecor Health, LLC Fluphenazine HCl Elixir, USP, 20 mg per 4 mL, Delivers: 10 mL recall: Failed Stability Specifications
Failed Stability Specifications
-
Class II · last month
Safecor Health, LLC Fluphenazine HCl Elixir, USP, 10 mg per 2 mL, Delivers: 10 mL recall: Failed Stability Specifications
Failed Stability Specifications
-
Class II · last month
Safecor Health, LLC Fluphenazine HCl Elixir, USP, 5 mg per 10 mL, Delivers: 10 mL recall: Failed Stability Specifications
Failed Stability Specifications
-
Class II · last month
Safecor Health, LLC Fluphenazine HCl Elixir, USP, 5 mg per 1 mL, Delivers: 10 mL recall: Failed Stability Specifications
Failed Stability Specifications
-
Class II · last month
Safecor Health, LLC Fluphenazine HCl Elixir, USP, 2.5 mg per 5 mL, Delivers: 5 mL recall: Failed Stability Specifications
Failed Stability Specifications
-
Class II · 5 months ago
Safecor Health, LLC Atomoxetine Capsules HCL, 10 mg Capsules in unit dose foil strip recall: Labeling: Label Mix-Up: Atomoxetine HCl 25mg Capsule incorrectly labeled
Labeling: Label Mix-Up: Atomoxetine HCl 25mg Capsule incorrectly labeled as Atomoxetine HCl 10mg Capsule.