# Major Recall Alert: FOLLTROPIN Injectable Kits for Cattle Recalled Due to Presence of Particulate Matter
## Why This Recall is Important
Vetoquinol USA, Inc. has initiated a voluntary recall affecting six lots of its FOLLTROPIN® Injectable Kits, a critical veterinary product used in cattle for superovulation. The recall stems from the discovery of particulate matter in the sterile diluent vials, found during routine annual sample inspections. This issue raises significant safety concerns for cattle treated with the product, as injectable medications containing particulate matter could potentially cause adverse reactions in animals, including injection site inflammation or hypersensitivity.
The FOLLTROPIN Injectable Kit is vital for the reproductive management of beef and dairy heifers and cows. However, this contamination issue underscores the importance of vigilance in ensuring veterinary product safety. To date, no adverse events linked to these recalled lots have been reported. Still, veterinarians and cattle farmers are urged to immediately discontinue the use of the affected batches to avoid any potential risks.
## Details of the Recall
Here’s what you need to know about the FOLLTROPIN recall:
- **Affected Product**: FOLLTROPIN Injectable Kits (porcine pituitary-derived follicle stimulating hormone for cattle).
- **Reason for Recall**: Presence of particulate matter in the sterile diluent vials.
- **Impacted Kits**: Six specific lots of FOLLTROPIN containing sterile bacteriostatic saline diluent.
- **Detection**: Contamination identified during routine inspection of retained samples.
- **Health Risks**: Possible pain, swelling, wounds at the injection site, fever, labored breathing, or decreased activity levels in treated animals. Contact a veterinarian immediately if you observe any of these symptoms.
It is essential to note that the FOLLTROPIN powder vials and the Dual Pack kits (which do not contain diluents) are **not impacted** by this recall.
The impacted FOLLTROPIN Kits were distributed across the U.S. through veterinary distributors.
## What You Should Do
If you possess any FOLLTROPIN Kits from the recalled batches:
- **Stop Use Immediately**: Do not use the affected product on cattle.
- **Quarantine the Product**: Isolate the recalled product to prevent accidental use.
- **Contact Vetoquinol USA**: For instructions on returning or properly disposing of the product, reach Vetoquinol USA, Inc. at 1-800-267-5707 (Monday–Friday, 8 a.m.–5 p.m. CST).
- **Report Issues to the FDA**: If you’ve experienced quality problems or adverse reactions, report them to the FDA at 1-888-FDA-VETS or [online](https://www.fda.gov/reportanimalae).
This recall is a precautionary step to ensure product safety and protect animal health. Vetoquinol USA is working closely with the FDA to address the issue. For more details, visit the official FDA recall announcement [here](https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/vetoquinol-usa-inc-recalls-six-lots-folltropin-injectable-kits-cattle-due-presence-particulate).
## Stay Safe – Get Instant Recall Alerts
Veterinary recalls, like this one, highlight the importance of staying informed about product safety updates. Protect your livestock and optimize your operations by staying ahead of potential health risks.
**Download Our Free Recall App** to receive **instant alerts** about veterinary product recalls, safety notifications, and best practices to ensure the well-being of your animals.
### Final Thoughts
The recall of FOLLTROPIN Injectable Kits serves as an important reminder of the need for regular monitoring and quality control in pharmaceutical products for livestock. Veterinarians and cattle farmers alike must act promptly to protect their animals’ health. Stay informed, stay vigilant, and stay prepared with up-to-date safety alerts at your fingertips.