Health Journal Online

Tag: Recalled

  • Dietary Supplement Sold at Sam’s Club Recalled as Salmonella Sickens 11 People

    Dietary Supplement Sold at Sam’s Club Recalled as Salmonella Sickens 11 People

    Sam’s Club is recalling all Member’s Mark “Super Greens” dietary supplement powders after a multistate salmonella outbreak sickened 11 people, federal health officials announced Friday.

    Three of those affected have been hospitalized, and the illnesses span seven states, including Florida, Kansas, Michigan, North Carolina, New York, South Carolina, and Virginia.

    The US Food and Drug Administration (FDA) and the Centers for Disease Control and Prevention (CDC) traced the outbreak to a single lot of organic moringa leaf powder imported from Vallon Farm Direct PVT LTD in Jodhpur, India.

    The moringa powder had been distributed to multiple suppliers across the country, ultimately reaching Sam’s Club stores nationwide and online.

    “The health and safety of our members is our top priority,” Sam’s Club said in a statement on November 3.

    “We moved quickly to remove this product from our impacted clubs as soon as we were notified by the supplier.”

    All Member’s Mark “Super Greens” powders are included in the recall, regardless of lot code or “best by” date, USA Today reported.

    Consumers in possession of the product are urged not to eat it and are advised to discard it or return it to the place of purchase for a full refund.


    FDA Probes Broader Moringa Recall

    Salmonella infections usually appear within 12 to 72 hours after consumption and can last four to seven days.

    Symptoms include diarrhea, fever, stomach cramps, and severe vomiting.

    According to the FDA, young children, older adults, and people with weakened immune systems are at the highest risk of severe illness.

    State health officials in Virginia and Michigan confirmed the presence of salmonella by testing samples collected from the homes of those who fell ill.

    The outbreak has been reported in cases dating from May to September. While most people recover without treatment, severe infections can require hospitalization, which happened in three of the 11 confirmed cases.

    According to AP News, Moringa, a plant native to India, is commonly used for its nutritional benefits, including protein, vitamins, minerals, and amino acids. Its dried leaves are often sold in powder form as a dietary supplement.

    The FDA cautioned that more products could be recalled as the investigation continues to determine if additional batches of moringa powder were contaminated.

    “Consumers should not eat the supplements and should throw them away or return them to the store for a refund,” the agency advised.

    Originally published on vcpost.com



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  • Eye Drops Recalled For Possible Fungal Contamination That May Affect Eyesight: FDA Warns

    Eye Drops Recalled For Possible Fungal Contamination That May Affect Eyesight: FDA Warns

    The U.S. Food and Drug Administration (FDA) has sounded the alarm on a nationwide recall of Systane brand eye drops, citing potential fungal contamination that could pose serious risks to eyesight.

    Systane Lubricant Eye Drops Ultra PF, commonly used to temporarily relieve burning and irritation caused by dry eye symptoms, is now at the center of a nationwide recall. The product was distributed to multiple retail stores and online platforms.

    Manufacturer Alcon Laboratories initiated the voluntary recall after a consumer reported foreign material inside a sealed single-use vial, which was later identified as fungal contamination.

    “Fungal contamination of an ophthalmic product is known to potentially cause eye infections. If an infection occurs, it may be vision-threatening, and in very rare cases potentially life-threatening in immunocompromised patients,” the FDA stated in a news release.

    The FDA has confirmed that no adverse events related to the recall have been reported so far. However, individuals experiencing quality issues or adverse reactions after using the product are encouraged to report them through the FDA’s MedWatch Adverse Event Reporting program. Complaints can be submitted online, by downloading and mailing the form, or via fax at 1-800-FDA-0178.

    Each cardboard box of the product contains 25 sterile, single-use vials of lubricant solution for ophthalmic use. “The affected Systane Lubricant Eye Drops Ultra PF, Single Vials On-the-Go, 25 count is limited to lot number 10101, expiration date 2025/09. The product can be identified by the green and pink carton design, the presence of “Systane” and “ULTRA PF” brand names on the front of the carton, and the “25 vials” package size,” the news release stated.

    Consumers who still have the products with them are advised to stop usage immediately and return to the place of purchase for a replacement or refund. Those who experience any issues potentially linked to the use of these eye drops should seek advice from a healthcare provider without delay.

    As Alcon conducts its investigation, a spokesperson told NBC News that “the presence of foreign material appears to be isolated to the single unit returned by a customer.” They emphasized that the recall is being carried out, “out of an abundance of caution to prioritize consumer safety.” Those who have issues with the product can also contact them at 800-241-5999.

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