Imprimis NJOF, LLC Dexamethasone Moxifloxacin, 1 mg/mL and 5 mg/mL recall: Presence of particulate matter - Glass like particles
Presence of particulate matter - Glass like particles.
The hazard: Foreign material — glass
This is a foreign-material recall — glass where there should be none. An affected pack looks identical to a sound one from the outside.
What the notice says: Presence of particulate matter - Glass like particles.
Why it matters: Pieces of glass may be inside the product. The risk here is physical rather than microbial: cuts to the mouth or throat, a broken tooth, or an injury further down if a fragment is swallowed.
Symptoms and when to call a doctor
If someone has swallowed a fragment and has mouth or throat pain, trouble swallowing, chest or stomach pain, vomiting, or blood in saliva or stool, they should be seen the same day. A fragment swallowed without symptoms usually passes on its own, but tell the clinician exactly what the product was: glass is usually visible on an X-ray, and a swallowed shard is one of the cases where imaging is worth doing.
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-0249-2026
- Published
- January 14, 2026
- Risk level
- Class II
- Status
- Ongoing
- Issued by
- U.S. Food and Drug Administration
- Brand
- Imprimis NJOF, LLC
- Product type
- Prescription & OTC drugs
- Units affected
- 778 boxes of 15,540 pre-filled syringes
- Distribution
- Nationwide
- Made in
- United States
- Lot / code info
- Lot: 25MAY051, Expires: 06/26/2026; 25AUG003, Expires:08/07/2026
Products covered by this recall
Dexamethasone Moxifloxacin, 1 mg/mL and 5 mg/mL, 1 mL Intraocular Injection, Rx only, Imprimis NJOF, LLC, Ledgewood, NJ 07852, NDC 71384-512-0.1
Check your product
The notice names 11 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.
- 25MAY051
Best-by / use-by date
Printed beside the lot code, not on the price sticker.
- 06
- 26
- 2026
- 08
- 07
- 540 pre-fill
NDC number
On the carton and again on the bottle or blister label.
- 71384-512-0
Package size
Match the net weight or the piece count on the front of the pack.
- 1 mg
- 5 mg
- 1 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 Glass pieces
Imprimis NJOF, LLC — This is a foreign-material recall — glass where there should be none. An affected pack looks identical to a sound one from the outside.
- Stop eating it, and do not pick through it to find the fragment — sorting it by hand is how people get cut.
- Check the freezer and the pantry for other packs carrying the same codes before you consider the matter closed.
- If someone has already bitten into something hard, have them stop, spit out what is in their mouth and rinse rather than swallow.
- Keep the pack if you can. If anyone was hurt, the fragment and the packaging together are the evidence that matters.
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: Imprimis NJOF, LLC — 1705 Route 46 Ste 6B, Ledgewood, NJ, 07852-9720
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 Imprimis NJOF, LLC prescription & otc drugs recalled?
Presence of particulate matter - Glass like particles. Presence of particulate matter - Glass like particles.
How do I know if I have the recalled product?
Match the codes printed on your package against the notice: lot code 25MAY051; best-by date 06 or 26. 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?
Stop eating it, and do not pick through it to find the fragment — sorting it by hand is how people get cut.
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.
Related recalls
-
Class II · 9 months ago
Tri-Moxi+¿ Single-Use Intraocular Injection, Imprimis NJOF, LLC recall: Presence of particulate matter - Glass like particles
Presence of particulate matter - Glass like particles.
-
Class II · 9 months ago
Imprimis NJOF, LLC Dexamethasone Moxifloxacin Ketorolac, 1 mg/mL, 0.5 mg/mL recall: Presence of particulate matter - Glass like particles
Presence of particulate matter - Glass like particles.
-
Class III · 11 months ago
Imprimis NJOF, LLC Klarity-C Drops 0.1%, Preservative-Free Sterile Ophthalmic Emulsion recall: Subpotent Drug
Subpotent Drug
-
Class II · 11 days ago
K.C. Pharmaceuticals, Inc. Sterile Lubricant Dry Eye Relief Eye Drops, 0.5 FL OZ recall: Lack of Assurance of Sterility
Lack of Assurance of Sterility
-
Class II · 11 days ago
Carolina Infusion, LLC Quad-Mix Injectable, Packaged in single-use dosage syringes recall: Lack of Assurance of Sterility: Related to processing equipment used
Lack of Assurance of Sterility: Related to processing equipment used in compounded product.
-
Class II · 11 days ago
Carolina Infusion, LLC Tirzepatide/Cyanocobalamin 26/2 MG/ML Injectable recall: Lack of Assurance of Sterility: Related to formulation using bacteriostic
Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product.