Louisiana recalls

Baxter Healthcare is recalling two lots of famotidine injection (20 mg in 50 mL sodium chloride) due to deviations from manufacturing standards. The affected lots may not meet quality and sterility requirements.

Baxter Healthcare Corporation is recalling specific lots of Clindamycin Injection USP in 5% Dextrose due to deviations from current Good Manufacturing Practice (CGMP) standards during production. The affected lots are NC193764 (expiration 10/18/2027) and NC195232 (expiration 11/25/2027), distributed nationwide in the US, Puerto Rico, and Chile.

Baxter Healthcare is recalling one lot of Daptomycin in 0.9% Sodium Chloride Injection due to deviations from good manufacturing practices (CGMP) during production. The affected lot (NC188692, expiring 11/22/2027) was distributed nationwide, in Puerto Rico, and Chile. No injuries have been reported.

Baxter Healthcare is recalling specific lots of MYXREDLIN (insulin human injection) due to deviations from current Good Manufacturing Practice (CGMP) standards during production. The affected lots were distributed in the US, Puerto Rico, and Chile. No injuries have been reported.

Baxter Healthcare Corporation is recalling five lots of Vancomycin Injection USP in 5% Dextrose due to Current Good Manufacturing Practice (CGMP) deviations identified during manufacturing. The affected lots were distributed nationwide, in Puerto Rico, and Chile.

Golden State Medical Supply Inc. is recalling Prasugrel HCI 10mg tablets (lot GS062298, expiration 09/30/2026) because they failed to meet dissolution specifications during quality testing. Dissolution is how quickly a tablet breaks down in the body to release its active ingredient. Tablets that dissolve too slowly or incompletely may not work as intended.

Food to Live Organic SuperGrass Powder in 6 oz, 12 oz, 1 lb, and 4 lb containers has been recalled due to Salmonella contamination. The affected products were distributed across the United States and U.S. Virgin Islands. No illnesses have been reported.

BMC Medical Co., Ltd. recalled 20,160 Luna G3 APAP sleep apnea devices (Model LG3600) due to a firmware defect in version G3-2.00.76. Under certain high-pressure, high-breathing-rate conditions, affected devices can display an error message and shut down automatically, stopping therapy delivery. Most devices were corrected with a firmware upgrade, but up to 196 units may still contain the defective version.

Foods Alive Inc is recalling 8-ounce packages of organic moringa leaf powder because they may be contaminated with Salmonella. The contamination was discovered after the supplier's sample tested positive. No illnesses have been reported so far.

SUPPLX.com's Business Pill and Branch Manager for Men dietary supplements contain yohimbine that is not listed on the labels. FDA testing found dangerously high levels of this substance, which can cause serious heart problems, severe high blood pressure, and other dangerous side effects—especially in people taking stimulants or certain medications.

American Regent is recalling three lots of epinephrine injection (1 mg/mL multi-dose vials) due to leaking and cracked vials, plus contamination with particles including nylon, cellulosic, acrylic, polyethylene, and glass. These particles can block blood vessels, cause blood clots, and damage organs; cracked vials also risk loss of sterility and bacterial contamination. No adverse events have been reported so far.

Certain Mondraker mountain bicycles equipped with ONOFF S9 Carbon MTB handlebars may have handlebars that crack or fracture during use. This can cause loss of control and a fall. The company has received five reports of handlebar breakage, including two injuries from falls.

Clorox Puerto Rico is recalling about 6.3 million bottles of scented Mistolin and Lestoil cleaners sold in Puerto Rico and the U.S. Virgin Islands. The products may contain Pseudomonas aeruginosa bacteria, which can cause serious infections in people with weakened immune systems or external medical devices if the bacteria is inhaled, touches the eyes, or enters through a break in the skin. People with healthy immune systems are typically unaffected.

The lithium-ion battery in XO Poppy Power Trip Magnetic Wireless Power Banks (model PYPBK5M) can overheat and catch fire. About 32,400 units were sold at TJX and Marshalls stores in three colors: cream, cream with pink bow print, and black with teddy bear print. No injuries have been reported.

The black eyes on this teether can detach when frozen, creating a choking risk for babies. Skip Hop has received four reports of eyes coming off, though no injuries have been reported yet.

These squishy toys contain water beads that can expand if swallowed, potentially causing choking, intestinal blockage, and serious injury or death. The toys are translucent squishy balls with cartoon faces, sold in tan bamboo steamer-shaped containers.

OKK Trading's Rainbow Mystery Squishy Bun Toys contain water beads that can expand larger than safe limits. If a child swallows a water bead, it can cause choking, intestinal blockage, and serious injury or death.

Gizoon Direct six-drawer dressers can tip over if not anchored to the wall, creating a risk of serious injury or death to children. The dressers do not meet federal safety standards for furniture stability.

The backrests on certain Branch height-adjustable ergonomic chairs can detach due to incorrectly installed anchors at the factory. This poses a fall hazard. The chairs were made between September 10, 2025 and April 22, 2026. Branch has received 11 reports of backrest detachment but no injuries so far.

Certain Amana brand through-the-wall air conditioners and heat pumps can develop a short circuit in the snubber component, which may emit flames. Two incidents of this short circuit have been reported, though no injuries have occurred yet.

Loyoda adult portable bed rails do not meet federal safety standards for adult bed rails. They pose a risk of serious injury or death from entrapment and asphyxiation.

SHEIN Distribution Corporation is recalling spiral toys that contain small plastic balls. These toys are intended for children under three years old, but the small balls pose a serious choking hazard and violate federal safety rules for that age group.

The lithium-ion batteries in Cambridge Audio Yoyo (M) Portable Bluetooth Speakers can overheat and catch fire. The company has received four reports of fires, smoke, and battery material ejection, though no injuries have been reported so far.

These wooden dressers can tip over and trap children if not securely anchored to the wall. The dressers do not meet federal safety standards for clothing storage furniture. No injuries have been reported.

Great Value Organic Triple Berry Blend (10 oz, lot code 6040 01-6) may be contaminated with E. coli O145, a harmful bacteria that can cause severe stomach cramps, bloody diarrhea, and vomiting. The contaminated berries were distributed to Walmart stores in 16 states. No illnesses linked to this specific product have been reported so far.

Northwest Naturals has recalled two frozen raw pet food products because they may be contaminated with Salmonella and/or Listeria monocytogenes. The affected products are the Frozen Chicken Recipe (cat food, 2 lb. bags) and Frozen Raw Diet for Dogs Chicken Recipe (6 lb. bags) in specific lots. No illnesses have been reported so far.

Everything Sprouts, LLC is recalling certain lots of Robust Radish Sprout Mix (5oz cups) sold in Minnesota and Wisconsin from August 13–26, 2026, because they may contain Shiga toxin-producing E. coli (STEC) or Salmonella bacteria. No illnesses have been reported to date.

B. Braun Medical Inc. is recalling three lots of 0.9% Sodium Chloride Injection (saline solution) used in hospitals and healthcare settings. The recalled product contains particles of zinc oxide that should not be present. Intravenous fluids contaminated with particulate matter can cause serious complications including blood clots and organ damage. No injuries have been reported so far.

Lipofit Extreme Fat Burner 2.0 (Lot 25M12F, expiration 09/2027) contains undeclared fluoxetine, a prescription antidepressant, in the daytime tablets and undeclared 2,4-dinitrophenol (DNP), a toxic pesticide, in the nighttime tablets. Neither ingredient is approved for use in dietary supplements, and DNP is not approved by the FDA for any use in humans.

Revival Animal Health recalled Breeder's Edge® and Shelter's Choice® Feline Milk Replacers because some batches contain low levels of potassium, copper, folic acid, choline, and/or vitamin B6. Young kittens depend entirely on milk replacer for nutrition, and these deficiencies can cause anemia, organ damage, and developmental problems within days or weeks.