Vetoquinol – FOLLTROPIN Injectable Kits for Cattle: Presence of particulate matter
Vetoquinol recalls six lots of Folltropin Injectable Kits for cattle due to particulate matter in the sterile diluent vials. Stop using immediately to prevent injection site reactions or hypersensitivity in animals.
Use caution until it’s fixed
Presence of particulate matter
Contact the company & request your remedy
What happened, in plain English
Vetoquinol is recalling six specific lots of Folltropin Injectable Kits for cattle because the sterile diluent vials contain particulate matter. This could cause injection site reactions or hypersensitivity reactions in animals if used. Read more at govinfonow.com/recall/1274713-vetoquinol-folltropin-injectable-kits-for-cattle-particulate-matter-recall.
Source Summary by GovInfoNow · govinfonow.com/recall/1274713-vetoquinol-folltropin-injectable-kits-for-cattle-particulate-matter-recall · Updated October 6, 2026 · Official notice: FDA pet food announcement (Nov 2025)
Cite this page
“Vetoquinol Folltropin Injectable Kits for Cattle: Particulate Matter Recall.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/1274713-vetoquinol-folltropin-injectable-kits-for-cattle-particulate-matter-recall. Based on FDA recall pet food announcement (Nov 2025) (https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/vetoquinol-usa-inc-recalls-six-lots-folltropin-injectable-kits-cattle-due-presence-particulate).
Why it’s dangerous
Particulate matter in the sterile diluent vials can cause injection site reactions or hypersensitivity reactions when administered to cattle. This may lead to symptoms like pain, swelling, fever, or labored breathing in affected animals.
Who’s affected
Veterinarians and cattle owners who have purchased the recalled Folltropin Kits from the impacted lots. Animals receiving the product may experience pain, swelling, fever, or labored breathing.
How to tell if you have this one
Check the Folltropin Kit carton for the lot number (e.g., 510578, 510579, etc.) on the outside. The product was sold between specific dates and expiration dates listed in the recall notice.
- Brand
Vetoquinol- Category
Pet food
What to do — step by step
Stop Using Immediately
Customers who have received Folltropin Kits from the impacted lots should stop using the product immediately to prevent potential injection site reactions or hypersensitivity.
Quarantine Product
Quarantine the recalled Folltropin Kits to prevent accidental use until you contact Vetoquinol USA for return or disposal instructions.
What FDA says to do
Customers who have received FOLLTROPIN Kits from the batches impacted by this recall should stop using the product immediately and quarantine product subject to recall.
Questions people ask
Why is this product being recalled?
The recall is due to the presence of particulate matter in the sterile diluent vials of the Folltropin Kits, which could cause injection site reactions or hypersensitivity reactions in cattle.
What are the symptoms of an adverse reaction?
Possible symptoms include pain and/or swelling/wounds at the injection site, decreased activity level, fever, and/or labored breathing in affected animals.
Are the Folltropin powder vials affected?
No, the Folltropin powder vials are not impacted by this recall as Vetoquinol has not identified any issues with them.
Contact Vetoquinol
We’ve drafted a message you can send Vetoquinol to request your refund or repair — edit it as you like.
Subject: Recall petfood:vetoquinol-usa-inc-recalls-six-lots-folltropin-injectable-kits-cattle-due-presence-particulate — Vetoquin Hello, I own a Vetoquinol that is covered by recall petfood:vetoquinol-usa-inc-recalls-six-lots-folltropin-injectable-kits-cattle-due-presence-particulate from Vetoquinol. The official recall notice states: Customers who have received FOLLTROPIN Kits from the batches impacted by this recall should stop using the product immediately and quarantine product subject to recall. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall pet food announcement (Nov 2025) (November 26, 2025)
- Plain-language summary written by qwen3:4b on October 6, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.