Wyoming recalls

Sold nationwide. DREO is recalling about 338,800 DR-HSH015 space heaters in the U.S. because they can overheat and ignite. The recall covers units made from April 2025 through January 2026, with the manufacture date and model number on a label on the underside. DREO has received 17 reports of the heaters catching fire, including three cases of property damage and one hand burn injury.

Serious·CPSC·Oct 29, 2026·DREO

Sold nationwide. Ariston Canada, formerly NTI Boilers, is recalling certain NTI and HTP gas boilers. A cracked condensate dish can let unburned gas build up inside the sealed cabinet, and if that gas ignites, the front cover can suddenly come off. The company has received 34 reports of the dish breaking, including three reports of the cover detaching, and one technician was seriously injured.

Serious·CPSC·Oct 29, 2026·Ariston

Sold nationwide. Whatever Works is recalling about 8,709 microwave grillers because they can overheat and ignite. The company has received three reports of grills catching fire, and no injuries have been reported. The grills were sold on Whateverworks.com from January 2025 through June 2026 for about $22.

Serious·CPSC·Oct 29, 2026·Whatever Works

Sold nationwide. SOOWERY is recalling about 138 8-drawer fabric dressers sold on Amazon from December 2025 through August 2026 for about $106. The dressers can tip over if they are not anchored to the wall, which can cause serious injury or death to children, and they do not meet a mandatory federal safety standard. No injuries have been reported.

Serious·CPSC·Oct 29, 2026·SOOWERY

Sold nationwide. PILLANI is recalling about 25,762 U-shaped nursing pillows sold on Amazon from April through September 2026. The pillows violate mandatory federal safety standards because they can obstruct an infant's breathing, which poses a serious risk of injury or death from suffocation. No injuries have been reported.

Serious·CPSC·Oct 29, 2026·Pillani

Sold nationwide. Fashion Brand Apparel is recalling about 300 QZH.DUAO children's pajama sets sold on Amazon.com from February through July 2026 for about $23. The sets do not meet mandatory federal safety standards for children's sleepwear, so they can pose a risk of serious burn injuries. No injuries have been reported.

Serious·CPSC·Oct 29, 2026·Fashion Brand Apparel

Sold nationwide. Pentax Medical is recalling five products: four PENTAX Medical ultrasound endoscope models and the PENTAX Medical OS-H5 water bottle assembly, about 3,140 units in total. The agency's warning labeling was updated to say users must make sure deaerated sterile water is in the assembly before and during procedures. No injuries have been reported.

Moderate·FDA·Oct 28, 2026·Pentax5 products

Sold nationwide. Abiomed is recalling 900 Impella heart pump controllers in three products: Automated Impella Controller, Impella Optical Controller, and Impella Connect Optical AIC. The units need hardware, firmware, or software updates found during a review of servicing records. Possible problems include the controller failing to recognize the purge cassette, a sticking push button that can cause loss of console control, start-up failure, and a software defect that can show incorrect negative pressure readings. No injuries have been reported.

Serious·FDA·Oct 28, 2026·Abiomed3 products

Sold nationwide. American Regent Inc. is recalling one lot of BetaVet, a betamethasone injectable suspension for intra-articular use in horses, sold in 5 mL single-dose vials. The vial crimps or seal may be loose or defective, which could affect the container's integrity. The recall covers lot 26038L2C1 (expires July 2027) and was distributed nationwide; no injuries have been reported.

Moderate·FDA·Oct 28, 2026·BetaVet

Sold nationwide. JXK Enterprises, Inc. is voluntarily recalling Boner Bears Chocolate, Lot #BB21125, sold as a male enhancement product. FDA lab testing found sildenafil, the active ingredient in the prescription drug Viagra, which is not listed on the label. The product was sold nationwide online through www.elyxr.com.

Serious·FDA·Oct 28, 2026·Boner Bears

Sold nationwide. GF Blends is recalling three gluten-free baking mixes because they may contain wheat gluten that is not listed on the label. The products are sold as Gluten Free Truly AIP flour, bread mix and the EAT G.A.N.G.S.T.E.R pizza crust and flat bread mix, and were sold nationwide online at eatgangster.com, trulyaip.com and Amazon.com. No injuries have been reported.

Serious·FDA·Oct 28, 2026·Gluten Free Truly AIP3 products

Sold nationwide. Eagle Pharma Outsourcing is recalling two compounded IV infusion products nationwide: phenylephrine HCl (100 mg in 250 mL saline, 50 containers) and oxytocin (30 units in 500 mL saline, 5 containers). The company cannot assure that the products are sterile. No injuries have been reported.

Moderate·FDA·Oct 28, 2026·Eagle Pharma Outsourcing2 products

Sold nationwide. AvKARE is recalling one lot of amitriptyline hydrochloride 10 mg tablets because they failed dissolution specifications. The recall covers 3,534 cartons of 50-count unit dose cards distributed nationwide. No injuries have been reported.

Moderate·FDA·Oct 28, 2026·AvKARE

Sold nationwide. Medtronic is recalling three CareLink SmartSync products, including the programmer, RF head patient connector and Device Manager app, because a software problem can cause an inaccurate displayed longevity estimate for implanted pulse generators. No injuries have been reported. The recall covers about 61,000 units distributed worldwide.

Moderate·FDA·Oct 27, 2026·Medtronic3 products

Sold nationwide. BioMerieux is recalling a limited number of EMAG nucleic acid sample preparation instruments used in clinical labs. After updating to firmware SP4 Patch 2, a random software error (Error 10003, Heater timeout) can cause delayed or no results when analyzing clinical samples. No injuries have been reported.

Moderate·FDA·Oct 27, 2026·bioMérieux

Sold nationwide. Philips is recalling 9 Azurion imaging system models, including Azurion 3, 5, 7 and S configurations. Some of these PCs may contain solid-state drives (SSDs) that are not specified in the Medical Device File, which could lead to reduced reliability over time, such as loss of imaging, a blank or black display, or trouble storing or accessing images. No injuries have been reported. The recall covers units distributed in the US and many other countries.

Moderate·FDA·Oct 27, 2026·Philips9 products

Sold nationwide. Canon Medical Systems is recalling 15 Alphenix interventional angiography X-ray systems (model INFX-8000C). A software issue can cause an internal error if F-Store or image acquisition is performed while the clinical analysis function is in use. The systems were distributed to hospitals and facilities in 18 states.

Moderate·FDA·Oct 27, 2026·Canon3 products

Sold nationwide. Fei Fah Medical Manufacturing recalled its Ultra Strength Electric Medicated Balm because it did not meet FDA manufacturing quality standards (CGMP). The recall covers about 171,120 units sold nationwide in 70g and 10g sizes. No injuries have been reported.

Moderate·FDA·Oct 27, 2026·Fei Fah Medical Manufacturing

Sold nationwide. ABC Compounding Co. is recalling 19 antiseptic hand soap, antiseptic foam and hand-and-body wash products nationwide. The recall cites manufacturing practice violations (cGMP deviations), and no injuries have been reported. The products come from several makers and sellers, including ABC Compounding, and are sold under names such as Palm, Lynx, Aero Foamy, PRO CHEM and Chemseptic.

Moderate·FDA·Oct 27, 2026·ABC Compounding19 products

Sold nationwide. Greenwich Rx is recalling 4,319 vials of its 200 mg/mL glutathione injection (10 mL multi-dose vials, for subcutaneous use only) because they may be contaminated with microbes. The recall covers 12 lots with beyond-use dates from October 2 to November 26, 2026, distributed nationwide. No injuries have been reported.

Serious·FDA·Oct 27, 2026·Greenwich Rx

Sold nationwide. Philips North America has recalled Model 712010 devices due to a potential for the device to fail immediately after exposure, which could cause the system to stop working. Approximately 563 units are affected.

Moderate·FDA·Oct 26, 2026·Philips

Sold nationwide. Par Health USA's Argatroban Injection vials contain unwanted particles—including cellulose, polystyrene, plastic, stainless steel, or rubber stopper material—in the solution. The contamination affects multiple lot numbers distributed nationwide. No injuries have been reported.

Serious·FDA·Oct 26, 2026·Paragon 282 products

Sold nationwide. ValuHealth Extra Strength Pain Relief Acetaminophen 500 mg bottles have an incorrect label on the bottle itself. The outer carton correctly says "Acetaminophen 500 mg," but the label on the bottle says "Pain Relief PM" — a different product. This mismatch could cause confusion about what you're taking.

Moderate·FDA·Oct 26, 2026·Prodose

Sold nationwide. GSMS Incorporated is recalling 30-count packs of Carboxymethylcellulose Sodium 0.5% Lubricant Eye Drops (NDC 51407-945-30), made by Huons Co., Ltd. in South Korea. Testing detected polyethylene (PE)-related oligomers, so the product failed its impurities and degradation specification. No injuries have been reported.

Moderate·FDA·Oct 26, 2026·Huons

Sold nationwide. Strides Pharma is recalling one lot of Cinacalcet 30 mg tablets because they failed to meet dissolution specifications, meaning the tablets may not break down properly in the body. This could result in inconsistent or reduced drug effectiveness. The affected lot is 7717825A, expiring 11/30/2028.

Moderate·FDA·Oct 26, 2026·Strides

Sold nationwide. Macleods Pharma USA is recalling specific lots of Olmesartan Medoxomil, Amlodipine, and Hydrochlorothiazide combination tablets (40 mg/10 mg/12.5 mg) because they failed to meet dissolution specifications. This means the tablets may not break down properly in the body, potentially reducing how well the medication works.

Moderate·FDA·Oct 26, 2026·MacLeods Pharma

Sold nationwide. Tonight We Ride, LLC recalled all lots of Ultimate Forza Male Supplement capsules because they contain three undeclared active ingredients: sildenafil and tadalafil (prescription drugs sold as Viagra and Cialis) and dapoxetine (not approved by the FDA). These ingredients were found through third-party testing and pose health risks, especially for people taking nitrate medications or with heart conditions.

Serious·FDA·Oct 24, 2026·Tonight We Ride

Sold nationwide. Certain Ziehm Orthoscan VERSA accessory carts and Versa Mini C-Arm systems have welds that do not meet specifications. This defect could cause the monitor arm mounting structure to separate from the cart during use.

Moderate·FDA·Oct 23, 2026·Ziehm Imaging

Sold nationwide. Medtronic has recalled certain OmniaSecure Model 3930M ventricular leads (used in heart devices for pacing and defibrillation) due to reports of difficulty achieving proper fixation during implantation. This implantation difficulty could potentially cause tissue trauma during the surgical procedure.

Moderate·FDA·Oct 23, 2026·Medtronic

Eden Brothers Broccoli Seeds (Calabrese variety) in 1 oz and 1 pound pouches may be contaminated with Salmonella. The affected product was packed in 2027 under lot numbers 1022067 and 1022068, and was distributed nationwide.

Serious·FDA·Oct 23, 2026·EDEN BROTHERS