Class II U.S. Food and Drug Administration

DermaRite Industries, LLC GelRite Instant Hand Sanitizer, Alcohol 65% recall: CGMP Deviation; manufactured at the same facility where other products

Recall published 11 months ago

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

The hazard: Labelling or manufacturing-practice failure

This recall is about what the packaging says rather than what is in it — which still matters, because the label is how a dose gets chosen.

What the notice says: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

Why it matters: The label, the strength printed on it, the barcode or the manufacturing records do not meet federal requirements. The practical danger is someone taking the wrong drug or the wrong dose while believing they have the right one.

Symptoms and when to call a doctor

If you may have taken a product that turned out to be a different drug or strength from the one on the label, call your prescriber, and call Poison Control on 1-800-222-1222 if you feel unwell. Describe what the pack said and what you actually took.

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-0166-2026
Published
November 26, 2025
Risk level
Class II
Status
Ongoing
Issued by
U.S. Food and Drug Administration
Brand
DermaRite Industries, LLC
Product type
Prescription & OTC drugs
Units affected
115,994 containers
Distribution
Nationwide
Made in
United States
Lot / code info
All lots on or before expiry date 08/2027

Products covered by this recall

GelRite Instant Hand Sanitizer, Alcohol 65%, packaged in a) 118 mL (NDC 61924-106-04), b) 473 mL (NDC 61924-106-16) and c) 800 mL (NDC 61924-106-27), and d) 1000 mL (NDC 61924-106-34) per container, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047.

Check your product

The notice names 13 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.

  • 2027 — 115
  • 994 containers

Best-by / use-by date

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

  • 08
  • 2027 — 115
  • 994 containers

NDC number

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

  • 61924-106-04
  • 61924-106-16
  • 61924-106-27
  • 61924-106-34

Package size

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

  • 118 mL
  • 473 mL
  • 800 mL
  • 1000 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 Labelling

DermaRite Industries, LLC — This recall is about what the packaging says rather than what is in it — which still matters, because the label is how a dose gets chosen.

  1. Compare the lot number and strength on your pack with the codes above and with what your prescription actually says.
  2. If what you were dispensed does not match your prescription, call the pharmacy before taking another dose.
  3. Keep taking the medicine as prescribed unless the notice or your prescriber says otherwise.
  4. Return the affected pack to the pharmacy for a replacement from a good lot.

Refunds and replacements

With medicines, a replacement supply matters more than cash, and that is what pharmacies are set up to provide.

  • Ask the dispensing pharmacy for a like-for-like replacement from an unaffected lot. This is the fastest route and usually costs nothing.
  • For a mail-order or online pharmacy, use the recall line listed on this page rather than the general support queue.
  • If the recall voided a fill you had already paid for, your insurer will normally authorise a replacement ahead of schedule. Quote the recall number.
  • If you paid out of pocket, ask for a refund of the co-pay or purchase price and keep the receipt the pharmacy issues.

Company contact: DermaRite Industries, LLC — 7777 W Side Ave, North Bergen, NJ, 07047-6436

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 DermaRite Industries, LLC prescription & otc drugs recalled?

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated. CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

How do I know if I have the recalled product?

Match the codes printed on your package against the notice: lot code 2027 — 115, 994 containers; best-by date 08 or 2027 — 115. 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?

Compare the lot number and strength on your pack with the codes above and with what your prescription actually says.

Can I get my money back?

Ask the dispensing pharmacy for a like-for-like replacement from an unaffected lot. This is the fastest route and usually costs nothing.

Where was the recalled product sold?

It was distributed nationwide.

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