Colorado recalls

Sold nationwide. PH Labs is recalling two dietary supplements, Ocular Plus and Vista MAX, because they contain Yellow No. 5 dye that is not listed on the label. Ocular Plus was distributed by L.A. Farmacia Natural and Vista MAX by Vision of Health, with about 6,967 units of each affected. The products went to two local retail stores, and no injuries have been reported.

Moderate·FDA·Jul 8, 2026·PH Labs2 products

Mars Snacking is recalling two MorningStar Farms vegan products, Buffalo Chik'n Nuggets and Hot & Spicy Sausage Patties, because they may contain pieces of plastic. Both are sold in resealable plastic bags and were distributed in many U.S. states and Puerto Rico. No injuries have been reported.

Moderate·FDA·Jul 8, 2026·MorningStar Farms2 products

Sold nationwide. MOGO Pure Moringa Oleifera capsules may be contaminated with Salmonella Typhimurium. The contamination was discovered during testing. Affected bottles were sold online through Amazon, eBay, Etsy, and mogomiranga.com.

Serious·FDA·Jul 8, 2026·MOGO

Sold nationwide. Cipla USA is recalling specific lots of Cinacalcet Hydrochloride 30 mg tablets because they contain elevated levels of N-nitroso-cinacalcet, a manufacturing impurity that exceeds FDA safety limits. The affected bottles were distributed nationwide.

Moderate·FDA·Jul 8, 2026·Cipla3 products

Sold nationwide. Lannett Company distributed amphetamine extended-release capsules that contained only immediate-release pellets but were labeled as extended-release. This labeling error could result in incorrect dosing and medication timing for patients who depend on the extended-release formulation.

Moderate·FDA·Jul 8, 2026·Lannett

Sold nationwide. Asclemed USA Inc. is recalling two lidocaine HCl 1% injection products in 5 mL single-dose ampules, sold nationwide. One is sold as Accucaine kits and the other is an unbranded lidocaine injection; both were distributed by Enovachem Pharmaceuticals. The recall was issued because the products may not be sterile, and no injuries have been reported.

Moderate·FDA·Jul 8, 2026·Asclemed USA Inc.2 products

Sold nationwide. Accord Healthcare is recalling one lot of levothyroxine sodium 300 mcg tablets because they may contain less active ingredient than labeled. This means the medication may not work as intended for patients who need it to manage thyroid conditions.

Moderate·FDA·Jul 8, 2026·Accord Healthcare

Sold nationwide. Lupin Pharmaceuticals is recalling multiple lots of prednisolone acetate ophthalmic suspension 1% (an anti-inflammatory eye drop) due to the presence of a foreign substance in some bottles. The affected lots were distributed nationwide. No injuries have been reported.

Moderate·FDA·Jul 8, 2026·Lupin

Sold nationwide. Accord BioPharma is recalling one lot of IMULDOSA (ustekinumab-srlf) injection due to lack of assurance that the product is sterile. The affected lot may not meet sterility standards required for injectable medications. No injuries have been reported.

Moderate·FDA·Jul 8, 2026·ACCORD BIOPHARMA INC

Sold nationwide. CareFusion is recalling 10 antiseptic skin prep products sold as BD ChloraPrep (Hi-Lite Orange, Clear and Scrub Teal), BD PurPrep, and ChloraPrep FREPP. Applicators that were meant to be sterilized before use were instead shipped to customers outside the intended distribution channel, so they may not be sterile. No injuries have been reported.

Moderate·FDA·Jul 8, 2026·CareFusion10 products

Sold nationwide. Lupin Pharmaceuticals is recalling certain lots of its Glucagon Emergency Kit because the syringe plunger may not move smoothly during use. This defect was discovered during stability testing and could prevent the kit from working properly in an emergency.

Moderate·FDA·Jul 8, 2026·Lupin

Sold nationwide. Mars Petcare discovered that two lots of Pedigree High Protein Chopped Chicken & Duck Flavor wet dog food were fraudulently diverted into stores after being sent for destruction due to quality concerns. The affected cans may contain pieces of sharp metal and plastic that could harm dogs if eaten.

Serious·FDA·Jul 3, 2026·Pedigree

Sold nationwide. Winco Fireworks International is recalling Roman Candles 8 Shot fireworks (Model RCLR-W8012) because they can malfunction. During use, shots may blow out the side of the tube instead of firing normally, creating a risk of serious injury from explosions and burns.

Serious·CPSC·Jul 2, 2026·Winco Fireworks

Sold nationwide. Winco Fireworks International is recalling Unity 7 Shot 200 Gram Aerial Cake fireworks (model MEF6096) because they can tip over during use, creating a risk of serious injury from explosion and burns. The affected fireworks were sold in red, white and blue packaging at Pyro City and independent fireworks retailers nationwide between January and May 2026.

Serious·CPSC·Jul 2, 2026·Winco Fireworks

Sold nationwide. Small metal wire bristles can detach from Cuisinart grill brushes during use and stick to food or the grill. If swallowed, these bristles can cause serious internal injuries requiring surgery. Conair has received 54 reports of detached bristles, including 3 cases where consumers needed medical treatment to remove bristles from their throat or digestive tract.

Serious·CPSC·Jul 2, 2026·Conair

Sold nationwide. Junpower CR2032 lithium coin batteries sold on Amazon lack the child-resistant packaging and warning labels required by federal law. If swallowed, these batteries can cause serious internal injuries or death. About 67,000 units were sold between December 2023 and September 2024.

Serious·CPSC·Jul 2, 2026·JSNJ_Tech

Sold nationwide. The LED board inside Metalux Optimized High Bay light fixtures can overheat or contact the lens and nearby combustible materials, creating a fire hazard. The company has received nine reports of these fixtures catching fire. About 42,000 fixtures sold since April 2020 are affected.

Serious·CPSC·Jul 2, 2026·Cooper Lighting

Sold nationwide. The clear plastic dome on this toy can detach from the base, exposing small plastic balls inside that children can choke on. Target has received nine reports of the dome detaching, including one incident where a child began to choke.

Serious·CPSC·Jul 2, 2026·Target

Sold nationwide. AMASKY nursing pillows sold on Amazon can obstruct an infant's breathing during feeding or tummy time. The pillows do not meet federal safety standards for nursing pillows and infant support cushions. About 4,000 pillows are affected.

Serious·CPSC·Jul 2, 2026·Pretty-Life

Sold nationwide. The lithium-ion battery in certain Rowenta X-Force Flex cordless vacuum cleaners can overheat and ignite, creating a risk of fire and burn injuries. The recall affects two models sold between July 2023 and January 2026.

Serious·CPSC·Jul 2, 2026·Rowenta

Sold nationwide. These LED finger light toys contain button cell batteries that children can easily access and swallow. Swallowing button cell batteries can cause serious internal injuries, including chemical burns, and can be fatal.

Serious·CPSC·Jul 2, 2026·POPOOO

Sold nationwide. CVS Health Medicated Hemorrhoidal Wipes contain lidocaine and are required to have child-resistant packaging by federal law, but this product does not. Young children could open the wipes and ingest the contents, causing serious injury or death. No injuries have been reported.

Serious·CPSC·Jul 2, 2026·Diamond Wipes

Sold nationwide. Topyond pool drain ports with covers do not meet federal safety standards and pose a risk of entrapment and drowning. The plastic drain ports (model SP-2850V) were sold online starting in May 2024 and do not provide adequate protection against the hazards they are designed to prevent.

Serious·CPSC·Jul 2, 2026·Topyond

Sold nationwide. Vevor baby loungers have sides that are too low to safely contain an infant and openings at the foot that are wider than safety standards allow. The loungers also lack a stand, creating a fall hazard if placed on elevated surfaces. These defects violate mandatory infant sleep product safety standards and can cause serious injury or death.

Serious·CPSC·Jul 2, 2026·Vevor

Sold nationwide. Kao USA recalled select lots of Oribe Serene Scalp Densifying Shampoo (8.5 oz and 33.8 oz) made between February 21–26, 2026 after detecting Pluralibacter gergoviae bacteria. People with weakened immune systems may be at higher risk of infection.

Moderate·FDA·Jul 1, 2026·Kao

Sold nationwide. Eunha Fisheries is recalling certain sliced Korean halibut and flounder sashimi products because the included soy sauce and vinegar red pepper paste packets contain wheat, soy, and sesame allergens that are not labeled on the individual condiment packets themselves. People with allergies or sensitivities to these allergens could have a serious or life-threatening reaction.

Moderate·FDA·Jul 1, 2026·Eunha Fisheries

Sold nationwide. Abiomed is recalling four Impella CP product sets that include 14 Fr Low Profile Introducer Kits, with 195 affected units in total. The introducer may form blood clots (thrombus) during prolonged use. No injuries have been reported, and the distribution covers the US states of FL, IL, MN, NJ, NY, and VA, plus Japan.

Serious·FDA·Jul 1, 2026·Abiomed4 products

Sold nationwide. Medline is recalling 16 convenience kits that contain 10mL polycarbonate colored syringes. The company found design changes to these kits that were not cleared by the FDA, and the products were not included in an earlier report. The kits were shipped nationwide and to Barbados, and no injuries have been reported.

Moderate·FDA·Jul 1, 2026·Medline16 products

Sold nationwide. Boston Scientific has recalled one INTERA 3000 Hepatic Artery Infusion Pump (model AP-0300H) due to the potential for leakage along the drug pathway from the pump through the catheter end. This is an implantable device used to deliver medication directly to the liver. The affected device was distributed in Ohio.

Moderate·FDA·Jul 1, 2026·Boston Scientific

Sold nationwide. Philips Telemetry Monitor 5500 (model 867232) devices may unexpectedly reset to a default state, causing them to lose their configuration settings and disconnect from the hospital's central monitoring system. This could prevent the monitor from reconnecting to the PIC iX central system until manually reconfigured.

Moderate·FDA·Jul 1, 2026·Philips