Animal IV Product Recall Issued Over Possible Fiber-Like Contamination

March 8, 2025 TruthUSA

Injected animals could face serious complications such as blood clots and strokes, which may lead to death.

A nationwide recall has been issued for an intravenous therapy product used in animals due to concerns about possible particulate matter, according to the U.S. Food and Drug Administration (FDA).

Based in Nebraska, Nova-Tech Inc. is recalling one lot of its Lactated Ringers Injection after discovering potential contamination with “fiber-like visible particles,” as stated in a recall announcement released by the FDA on March 4.

This injection is utilized for rehydrating or maintaining hydration in animals by replenishing lost fluids and restoring electrolyte balance. However, the presence of particulate matter in these injections may lead to severe health risks, the company advised.

Possible complications include “inflammation of a vein, granuloma, and obstruction of blood vessels in the heart, lungs, or brain, which can lead to stroke or critical blood clotting events, including death,” according to the recall notice.

“The likelihood and seriousness of these adverse effects can vary, depending on various factors such as the size and quantity of the particles in the drug, along with patient comorbidities (e.g., age, impaired organ function) and the presence or absence of vascular anomalies.”

This product is packaged in 5-liter IV bags, with 2 units per case, identified by lot code #C2411061 and set to expire in November 2026. It was distributed nationwide from December 31, 2024, to February 28, 2025.

Nova-Tech discovered the issue during visual inspections conducted for stability testing. Currently, there have been no reports of adverse events.

The company is “notifying its distributors and customers via email and regular mail and is coordinating the return of all recalled products.”

Veterinarians in possession of this injection should return it to the distributor, as indicated in the announcement.

Some symptoms of potential adverse events may include paralysis, vomiting, pain, difficulty breathing, loss of consciousness, decreased activity level, swelling, fever, and weakness.

“If you notice any of these or any other alarming symptoms in an animal that may have been given this product, please consult a veterinarian immediately.”

Consumers with questions regarding the recall can contact the company at 308-381-8841.

Previous recalls of Lactated Ringers Injection have been issued by the FDA due to contamination concerns.

In 2020, ICU Medical Inc., based in California, announced a nationwide recall of these injections due to the potential presence of iron oxide. This product was intended for both human and animal use.

Earlier in 2019, ICU Medical also recalled the injection due to “particulate matter” being present. This recall was focused on veterinary applications.

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