Adequan veterinary injections recalled for visible glass fibers — product photo from the FDA
Moderate riskFDA announcements

Adequan veterinary injections recalled for visible glass fibers

American Regent, Inc. Animal Health recalled four specific lots of Adequan Canine Injection (for dogs) and Adequan i.m. Injection (for horses) after discovering glass fibers in the products during internal testing. No adverse events have been reported to date.

From the FDA notice · Read the official notice ↗ · All American Regent recalls

What to do

  1. If you have one of the recalled lots (Canine: #3369 or #25011; i.m.: #24416 or #25265P), stop using it immediately.
  2. Contact your veterinarian if your pet has experienced pain, swelling, or infection at an injection site.
  3. Return unused product to the manufacturer or discard it.
  4. Call American Regent Customer Service at 800-645-1706 (Mon–Thu 8 AM–6 PM EST, Fri 8 AM–4 PM EST) with questions.

Is yours affected?

Compare your label or packaging with the recalled product.

Sold in
Nationwide
Made for
Pets

Photos from the FDA

Adequan® i.m. Injection (for horses), 500mg/5 mL single-dose 5mL vials
Adequan® i.m. Injection (for horses), 500mg/5 mL single-dose 5mL vials
Adequan® Canine Injection (for dogs), 100 mg/mL 5mL multi-dose vials
Adequan® Canine Injection (for dogs), 100 mg/mL 5mL multi-dose vials

Details

Illnesses reported
None reported

In the FDA's words

FOR IMMEDIATE RELEASE – July 31, 2026 – Shirley, NY, American Regent, Inc. Animal Health is conducting a nationwide recall of two lots ( 25011 and 3369 ) of Adequan® Canine Injection (for dogs), 100 mg/mL 5mL multi-dose vials and two lots ( 24416 and 25265P ) of Adequan® i.m. Injection (for horses), 500mg/5 mL single-dose 5mL vials to the consumer level. The products are being recalled due to the presence of glass fibers found during testing of internally retained samples.

Risk Statement : The administration of an intramuscular injectable product containing particulate matter, such as glass fibers, may result in local irritation, swelling, inflammation, injection site pain, infection, or abscesses. To date, American Regent, Inc. has not received any reports of adverse events related to the recalled lots.

Both Adequan Canine and Adequan i.m. are clear, colorless to slightly yellow solutions. The products are for intramuscular injections and are to be used by or under the direction of a licensed veterinarian.

Read the full announcement

Adequan Canine is a prescription medication used in the treatment of non-infectious degenerative or traumatic joint dysfunction in dogs.

Adequan i.m. is a prescription medication used in the treatment of noninfectious degenerative or traumatic joint dysfunction and associated lameness in horses.

Adequan Canine Lot #’s 3369 and 25011 were distributed nationwide to online pharmacies, distributors/ wholesalers and veterinarians in the United States on 05/22/2024 and 04/14/2025 respectively and Adequan i.m. Lot #’s 24416 and 25265P were distributed nationwide to online pharmacies, distributors/ wholesalers and veterinarians in the United States on 05/08/2025 and 01/22/2026 respectively.

Product Description

NADA

Lot #

Distribution Date

Expiration Date

Adequan Canine Injection, 100mg/1 mL 5 mL multi-dose vial

141-038

3369

05/22/2024

10/31/2026

Adequan Canine Injection, 100mg/1 mL 5 mL multi-dose vial

141-038

25011

04/14/2025

12/31/2027

Adequan i.m. Injection 500mg/5 mL 5 mL multi-dose vial

140-901

24416

05/08/2025

11/30/2027

Adequan i.m. Injection 500mg/5 mL 5 mL multi-dose vial

140-901

25265P

01/22/2026

03/31/2027

Any person or entity with the recalled product lots should not use the products.

Consumers : Stop using the recalled products lots. Contact your veterinarian if your pets have experienced any problems that may be related to using the recalled products.

Distributors and retailers : Stop distribution, return any leftover recalled product to the manufacturer, or discard.

Veterinary hospitals, clinics, and other consignees : Return any unused product to the manufacturer or discard.

CONTACT AMERICAN REGENT INC.

Consumers and veterinary professionals with questions regarding this recall can contact American Regent Inc. using the below information.

Area of Support

Contact Center

Contact Information

For detailed return/replacement/credit information

American Regent, Inc. Customer Service

Phone: 800-645-1706 (8:00AM-6:00PM EST, Monday – Thursday, 8:00AM-4:00PM EST, Friday) Email: cs@americanregent.com

To report adverse events

American Regent, Inc. Pharmacovigilance

Phone: 888-354-4857 (24 Hours/Day, 7 Days/Week) Email: animalhealth@americanregent.com

For product quality complaints

American Regent, Inc. Product Quality Complaints

Phone: 888-354-4855 (24 Hours/Day, 7 Days/Week) Email: pqc@americanregent.com

For medical questions

American Regent, Inc. Medical Information

Phone: 888-354-4857 (24 Hours/Day, 7 Days/Week) Email: animalhealth@americanregent.com

Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA at 1-888-FDA-VETS or online at http://www.FDA.gov/reportanimalae .This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

American Regent, Inc. is committed to the safety of patients who rely on its products and is taking this precautionary action to protect public health.

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