Colorado recalls

Sold nationwide. Medline is recalling four sizes of Micro-Kill Bleach Germicidal Bleach Wipes, about 1.07 million units in total. The bleach concentration in the wipes may drop below the labeled level before the 12-month shelf life ends, which could reduce their ability to kill germs.

Moderate·FDA·Aug 19, 2026·Medline4 products

Sold nationwide. Covidien is recalling five surgical suture products, including V-Loc 90, V-Loc 180, Dermalon, Surgipro and Surgipro II, with about 135,875 units affected. The sterile packaging may have a tear or hole, which could let germs reach the sutures and cause infection, prolonged surgery, or vision loss if used in eye surgery. The recall covers the US and many other countries, and no injuries have been reported.

Moderate·FDA·Aug 19, 2026·Covidien5 products

Sold nationwide. Black depth markings on the outer sheath of the coaxial dilator introducer in certain Boston Scientific Enhance transcarotid and peripheral access kits may detach. The recall covers about 114,260 kits across many lot numbers. No injuries have been reported.

Moderate·FDA·Aug 19, 2026·Galt Medical

Sold nationwide. Spacelabs Healthcare is recalling about 6,074 Xhibit Central Station units, model 96102, which are used to remotely monitor patient data. The recall involves a third-party DisplayPort audio/video splitter that can fail, interrupting audio and video output to extra displays. No injuries have been reported.

Moderate·FDA·Aug 19, 2026·Spacelabs Healthcare

Sold nationwide. Some GORE VIABIL Short Wire Biliary Endoprosthesis devices labeled as model VSWVN1010 (10 mm by 10 cm, without transmural drainage holes) are actually model VSWVH1006 (10 mm by 7 cm, with transmural drainage holes). The recall covers 13 units, sold in Georgia and Rhode Island, and no injuries have been reported. The device is used to keep the common bile duct open when it is blocked.

Moderate·FDA·Aug 19, 2026·Gore2 products

Sold nationwide. Ventana Medical Systems is recalling navify Digital Pathology software, version 2.5, used with the Roche Digital Pathology Dx slide imaging system. Customers reported that images did not match their information (metadata) in the viewer window. No injuries have been reported.

Moderate·FDA·Aug 19, 2026·Ventana Medical Systems

Sold nationwide. MicroVention is recalling certain BOBBY Balloon Guide Catheters because the balloons may develop pinhole defects, which occur at an increased rate. The catheter is used by health care providers to guide a catheter into blood vessels during peripheral and neurovascular procedures. The FDA has classified the recall as Class II, and no injuries have been reported.

Moderate·FDA·Aug 19, 2026·Microvention

Sold nationwide. Baxter Healthcare is recalling certain Duo-Vent solution sets (product code 1C8507) because air bubbles can form in the drip chamber and tubing. Customers reported this happening when a pressure cuff was in use or when the tubing was flushed with the clamp fully open. About 24,528 units were distributed nationwide, and no injuries have been reported.

Serious·FDA·Aug 19, 2026·Baxter

529 Commerce's aquafaba powder (vegan egg replacement) contains undeclared egg, which is a serious allergen risk. The product was distributed across 22 states. People with egg allergies who consume this powder could have an allergic reaction.

Serious·FDA·Aug 19, 2026·529 Commerce

Sold nationwide. Baxter Healthcare Corporation is recalling one lot of Cefazolin in Dextrose injection due to the presence of particulate matter in the solution. The affected product is a frozen premix infusion bag used for intravenous antibiotic treatment. This is a Class I recall, the most serious classification.

Serious·FDA·Aug 19, 2026·Baxter

Sold nationwide. Liebel-Flarsheim Company LLC is recalling Optiray Imaging Bulk Package-350 (ioversol injection 74%, 350 mg/mL) due to the presence of particulate matter—including plastic, stainless steel, and glass—found in affected vials. The contamination affects lot #25ZF3670 with an expiration date of May 31, 2027, distributed nationwide in the US and Mexico.

Serious·FDA·Aug 19, 2026·Liebel-Flarsheim

Sold nationwide. Victory Medical Center Pharmacy's Glutathione injectable solution (200 mg/mL) failed sterility testing and was found to contain elevated bacterial endotoxin levels, which are out of acceptable limits. The affected product was distributed nationwide in specific lots with expiration dates through August 2026.

Serious·FDA·Aug 19, 2026·Victory Medical Center Pharmacy

Sold nationwide. Buy-Herbal's Kian Pee Wan Capsules contain two prescription drug ingredients—dexamethasone and cyproheptadine—that are not listed on the label and were not approved by the FDA. The product was sold online through eBay. No injuries have been reported.

Serious·FDA·Aug 19, 2026·Buy-Herbal

Sold nationwide. Heritage Pharmaceuticals' clindamycin palmitate hydrochloride oral solution (75 mg/5 mL) has been recalled due to the presence of particles and white flakes found in reconstituted bottles. The affected lot is 2411550, which expires November 2026. This product was distributed nationwide.

Moderate·FDA·Aug 19, 2026·Heritage Pharmaceuticals

Sold nationwide. CLEAR EYES Maximum Itchy Eye Relief eye drops may not be sterile due to potential contamination. The affected product is the 0.5 fl oz (15 mL) dropper bottle, Lot 2552A with expiration date 09/30/2027. No injuries have been reported.

Moderate·FDA·Aug 19, 2026·Prestige Brands

Sold nationwide. Shoolin Pharma Chem LLP is recalling five bulk powder products, sildenafil citrate and tadalafil in 100-gram, 500-gram, and 1-kilogram sizes, sold for prescription compounding only. The recall was triggered by manufacturing practice (CGMP) deviations found during an FDA inspection, and no injuries have been reported. The products were distributed nationwide.

Moderate·FDA·Aug 19, 2026·Shoolin Pharma Chem5 products

Sold nationwide. Apollo Care is recalling 11 strengths of semaglutide sterile multi-dose vials for subcutaneous injection, all sold under the APOLLO care brand. The vials may contain particles identified as nylon/polyamide and silk-like material. The recall covers products distributed nationwide, and no injuries have been reported.

Moderate·FDA·Aug 19, 2026·Apollo Care11 products

Sold nationwide. One lot of Novartis Diovan (valsartan) 160 mg tablets failed to meet dissolution specifications, which means the tablets may not dissolve properly in the body. This could affect how well the medication works. The affected lot (AV5913C, expiring 6/2027) was distributed nationwide.

Moderate·FDA·Aug 19, 2026·Novartis

Sold nationwide. Dreyer's Grand Ice Cream is recalling select Outshine Fruit Bars because glass may have contaminated the product. The recall affects five flavors (Strawberry, Watermelon, Grape, Tangerine, and Black Cherry) in 6-count and 24-count variety packs. No injuries have been reported so far.

Moderate·FDA·Aug 18, 2026·Dreyer's

Sold nationwide. Gangothri Foods (operating as Indus Foods, LLC) recalled approximately 1,626 pounds of ready-to-eat pickled goat and chicken products made between January 2025 and May 2026 because they were produced without USDA inspection. The products were sold to restaurants, retailers, distributors, and consumers nationwide. No illnesses have been reported.

Serious·USDA·Aug 17, 2026·Gangothri

Sold nationwide. The fan blades on some Hampton Bay Halwin 52-inch ceiling fans can separate from the motor flywheel during operation. This poses a risk of impact or injury. The company has received 11 reports of blades breaking or separating, though no injuries have been reported yet.

Moderate·CPSC·Aug 13, 2026·Youngo

Sold nationwide. Sunnyside gallon 1-K Kerosene Heater and Appliance Fluid containers lack safety devices required by federal law and pose a risk of flash fire and serious burns. The recalled batch (26082) was sold online and at hardware stores from May through July 2026.

Serious·CPSC·Aug 13, 2026·Sunnyside

Sold nationwide. Zimtown 5-gallon portable gas cans sold online have closures that are not child-resistant, violating federal safety standards. Children could open the cans and spill fuel, risking serious burns and poisoning.

Serious·CPSC·Aug 13, 2026·Zimtown

Sold nationwide. SUGIFT pressure washers lack a safety device (GFCI) that prevents electrical shock. The short power cord may encourage users to connect an extension cord, which increases the risk of serious injury or death from electrocution.

Serious·CPSC·Aug 13, 2026·Sugift

Sold nationwide. CuberShop's Magnetic Stickerless Speed Cubes (model YJ MGC 5×5) come with loose high-powered magnets in the packaging. If swallowed by a child, these magnets can attract each other or metal objects and become trapped in the digestive system, potentially causing serious internal injury or death.

Serious·CPSC·Aug 13, 2026·Sky Cube

Sold nationwide. These yellow prank sound makers contain coin batteries that children can access and swallow. Swallowing these batteries can cause serious internal burns and death. The products also lack required safety warnings.

Serious·CPSC·Aug 13, 2026·Shengsen Toys

The metal insert in the front crown hole of Ritchey carbon bicycle forks can come loose. If this happens, an attached accessory can fall onto the front wheel, potentially causing the rider to crash.

Serious·CPSC·Aug 13, 2026·Ritchey

Sold nationwide. Qabefy-branded mattresses sold on Amazon fail to meet mandatory U.S. flammability safety standards, creating a risk of serious injury or death from fire. About 774 mattresses, sold between November 2025 and March 2026, are affected.

Serious·CPSC·Aug 13, 2026·Qabefy

Sold nationwide. GigaCloud's Merax Murphy beds can fall during assembly or disassembly if not properly installed, posing risk of serious injury. The company has received two reports of beds falling and injuring consumers. The recall affects full-size and twin-size models sold online from May 2024 through February 2026.

Serious·CPSC·Aug 13, 2026·GigaCloud

Sold nationwide. Yamazuki youth ATVs (model XW-A19, sold under QEASET or HOVERHEART brands) have faulty parking brakes that fail to hold, missing rear safety reflectors, and speed limiters not properly set for children. These defects create a crash hazard and increase the risk of serious injury or death.

Serious·CPSC·Aug 13, 2026·Yongkang Dingchang