Animal and Veterinary Recalls
ADM Animal Nutrition recalls ADM Animal Nutrition
ADM Recalls Select Pelleted Cattle Nutrition Feed Products
Specific lots may contain elevated or deficient levels of nutrients which may be harmful to cattle
CHICAGO, March 5, 2025 - ADM Animal Nutrition, a division of ADM (NYSE: ADM), is recalling specific pelleted animal feed products because they may contain elevated levels of copper or have levels of zinc below the represented amounts which could be harmful to cattle.
Possible impacts of chronic copper toxicity include: gastroenteritis characterized by anorexia, signs of abdominal pain, depression, lethargy, diarrhea, and dehydration. Possible impacts of zinc deficiency include: decreases in feed intake, feed efficiency, and growth.
No illnesses or deficiency impacts have been reported to date.
Nova-Tech, Inc. recalls Nova-Tech Lactate Ringers Injection 5000 mL
FOR IMMEDIATE RELEASE – March 4th, 2025 – Grand Island, Nebraska, Nova-Tech, Inc. is voluntarily recalling one (1) lot of Lactated Ringers Injection for Animal Use Only to the end user level. The Lactated Ringers Injection has been found to potentially contain fiber- like visible particles.
Risk Statement: Intravenous administration of an injectable product that contains particulate matter may result in serious adverse events. Potential complications related to injection of particles include inflammation of a vein, granuloma, and blockage of blood vessels in the heart, lungs or brain which can cause stroke or life-threatening blood clot events, including death. The frequency and severity of these adverse events could vary depending upon a variety of factors including the size and number of particles in the drug product, patient comorbidities (such as age, compromised organ function), and presence or absence of vascular anomalies.
Dietary Supplement Recalls
New York Wholesale Group recalls Zaarah Herbals Dietary Supplements
New York Wholesale Group of Hicksville, NY is recalling Zaarah Herbals Rasayan Churan, Zaarah Herbals Gurmar Powder, Zaarah Herbals Vasaka Powder, and Zaarah Herbals Bhringraj Powder to the consumer/user level because it has the potential to be contaminated with elevated levels of lead and arsenic. Short term exposures to very low levels of lead may not elicit any symptoms. It is possible that increased blood lead levels may be the only apparent sign of lead exposure. Additional overt signs and symptoms of lead exposure are more likely with acute exposure to higher levels of lead. While lead can affect nearly every bodily system, its effects depend upon the amount and duration of lead exposure and age/ body weight. If a fetus is exposed to enough lead for a protracted period(e.g., weeks to months) permanent damage to the central nervous system may occur. This can result in learning disorders, developmental defects, and other long-term health problems. For adults, chronic lead exposure is associated with kidney dysfunction, hypertension, increased risk of mortality from cardiovascular disease, and neurocognitive effects.
Consumption of inorganic arsenic has been associated with cancer, skin lesions, cardiovascular disease, and diabetes in humans. Inorganic arsenic exposure during fetal development, infancy, and childhood may contribute to neurodevelopment effects, as well as increase lifetime cancer risk.
Food and Beverage Recalls Cattle Feed
U.S. Trading Company recalls Joy Luck Dried Lily Flowers
(March 3, 2025) U.S. Trading Company of Hayward, CA is recalling Joy Luck Brand Lily Flowers because it may contain undeclared SULFITES. People who have an allergy or severe sensitivity to sulfites run the risk of serious allergic reaction if they consume these products.
The lily flowers were distributed to retailers Nationwide.
The recall was initiated after Florida Dept of Agriculture and Consumer Services collected a sample of the lily flowers. It was discovered that lily flowers containing sulfites were distributed in packaging that did not reveal the presence of sulfites
No illnesses have been reported to date.
Medical Device Recalls
Smiths Medical recalls Portex Intubation Oral/Nasal Endotracheal Tubes
MINNEAPOLIS, MN. March 7, 2025 – Smiths Medical has issued an Urgent Medical Device Correction to notify affected global customers of a potential issue with the 2.0, 2.5, 3.0 and 3.5 mm sizes of Intubation ORAL/NASAL Endotracheal Tube products being smaller than expected.
If the diameter of the device is smaller than expected, it may potentially result in inadequate ventilation to the patient, post-insertion of the endotracheal tube. In such situations, the patient may experience hypoxia, underdose, and/or cardiopulmonary collapse which may lead to death. To date, Smiths Medical has received eight (8) reports of serious injury that are potentially related to this issue.
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