Alaska recalls

Sold nationwide. Artivion recalled one CryoPatch SynerGraft pulmonary human cardiac patch (Model SGP010) because it came from a 64-year-old donor, which is older than the program's accepted range of newborn to 60 years. The patch was already implanted, and because long-term data on these patches are limited, early graft dysfunction cannot be ruled out. No injuries have been reported.

Moderate·FDA·Oct 30, 2026·Artivion

Sold nationwide. Illumina is recalling five diagnostic sequencing instruments and servers: NextSeq 550Dx, MiSeq Dx, NovaSeq 6000Dx, DRAGEN Server for NextSeq 550Dx, and VeriSeq Onsite Server V2. The recall covers about 2,700 units, all sold for in vitro diagnostic (laboratory testing) use. A cybersecurity weakness in how these devices communicate with customer-provided computers, storage, or servers could allow data transmission to be compromised. No injuries have been reported.

Moderate·FDA·Oct 30, 2026·Illumina5 products

Sold nationwide. Natus Medical is recalling Embletta MPR PG sleep monitors because the device may not correctly format its internal memory. Old study data may remain on the device and be updated with incorrect patient information, or recordings may fail to start or end early. No injuries have been reported.

Moderate·FDA·Oct 30, 2026·Natus Medical

Sold nationwide. Smith & Nephew recalled seven units of the EVOS 3.5MM Lateral Proximal Tibia Plate, 6 Hole Left, 91MM. The implants were labeled and laser etched as a standard lateral tibia plate, but they are actually a partial articular version. No injuries have been reported.

Moderate·FDA·Oct 30, 2026·Smith & Nephew

Sold nationwide. Accriva Diagnostics is recalling certain Hemochron Jr. APTT test cuvettes, used to check low-dose heparin levels in blood. The clot-activating reagent inside some cuvettes may be out of position or missing, which can cause error codes or falsely high results. Falsely high results could lead to a lower anticoagulant dose than needed, which could raise the risk of blood clots. No injuries have been reported.

Moderate·FDA·Oct 30, 2026·Accriva Diagnostics

Sold nationwide. Tandem Diabetes Care found that some Tandem Mobi insulin pumps can give false occlusion alarms when no blockage is present. This can cause the pump to stop insulin delivery until the user acknowledges the alarm and restarts therapy. Repeated interruptions could lead to high blood glucose, and in severe cases may require medical care or hospitalization.

Serious·FDA·Oct 30, 2026·Tandem Diabetes Care

Sold nationwide. House Foods America Corporation is recalling bulk vacuum-sealed seitan cubes because the labels leave out the ingredient list and wheat, a common allergen. The product, sold as two 5-pound packages per case and marked with code D2026OCT26, was shipped to nine distribution centers across the country. No injuries have been reported.

Serious·FDA·Oct 30, 2026·House Foods America

Sold nationwide. Pan Pepin, Inc. is recalling ParaBien Al Grano (UPC 0 21425 01513 4) because the product contains sesame, which is not listed on the label. The recall covers 3,127 units sold to customers in Puerto Rico. No injuries have been reported.

Serious·FDA·Oct 30, 2026·ParaBien

Sold nationwide. Preferred Pharmaceuticals is recalling certain lots of Artificial Tears Lubricant Eye Drops (labeled Visine, made by Geri-Care in Brooklyn, NY) because the manufacturer cannot assure the product is sterile. About 480 bottles were distributed nationwide. No injuries have been reported.

Moderate·FDA·Oct 30, 2026·Preferred Pharmaceuticals

Sold nationwide. AvKARE is recalling one lot of fludrocortisone acetate 0.1 mg tablets because testing found impurity or degradation levels above required limits. The recall covers lot 48353 (expiration 10/31/2026) in 50-tablet unit-dose cartons, NDC 50268-330-15, distributed nationwide. No injuries have been reported.

Moderate·FDA·Oct 30, 2026·AvKARE

Sold nationwide. Par Health USA is recalling certain lots of Brevital Sodium (methohexital sodium) for injection, a 500 mg multiple-dose vial sold in the US and Canada. The vials may contain particles identified as cellulose. No injuries have been reported.

Serious·FDA·Oct 30, 2026·Paragon 28

Sold nationwide. ArjoHuntleigh Polska is recalling about 8,780 Carevo height-adjustable shower trolleys, Model BAC1111-01. The side support panel can open unintentionally if the handles are not fully locked and extra force is applied during patient handling, which could cause a patient to fall and be seriously injured.

Moderate·FDA·Oct 29, 2026·Arjohuntleigh

Sold nationwide. Stryker Leibinger is recalling Precision Pointer Electromagnetic devices because the pointer tube can crack at a laser-welded joint during use. If that happens, loose parts could fall out while the device is inside a patient. No injuries have been reported.

Moderate·FDA·Oct 29, 2026·Stryker

Sold nationwide. Boston Scientific is recalling certain Nalu TD2 Therapy Discs and TD2 Patient Kits used with the Nalu Neurostimulation System. A firmware problem can cause the disc to try to restart and then fail, so it stops working. If no backup disc is available, the implanted pulse generator may also stop working, which could leave pain signals unblocked. No injuries have been reported.

Moderate·FDA·Oct 29, 2026·Boston Scientific

Sold nationwide. Novadoz Pharmaceuticals is recalling about 13,296 bottles of 1,000-count atorvastatin calcium 40mg tablets distributed nationwide. Some bottles may contain other tablets or capsules that are not atorvastatin. No injuries have been reported.

Moderate·FDA·Oct 29, 2026·MSN Laboratories

Sold nationwide. Brandywine Pharmaceuticals is recalling one lot of theophylline extended-release tablets, 100 mg, because stability testing for the product was interrupted at a third-party lab. Stability testing checks whether a medicine stays within its quality standards over time. No injuries have been reported.

Moderate·FDA·Oct 29, 2026·Brandywine Pharmaceuticals2 products

Sold nationwide. Meitheal Pharmaceuticals is recalling about 121,800 vials of Vecuronium Bromide for Injection, 10 mg, because the labels lack a required warning or prescription legend. No injuries have been reported. The FDA classified this as a Class III recall, which means it is unlikely to cause serious harm.

FDA·Oct 29, 2026·Meitheal Pharmaceuticals2 products

Sold nationwide. Direct Rx is recalling 493 jars of Lidocaine Ointment USP, 5.0%, 50g, because the product may contain less lidocaine than its label states. The affected lots are 03AP2511, 30AP2518, 18JU2519, and 18JU2520, with an expiration date of 04/30/2027. The product was distributed nationwide, and no injuries have been reported.

Moderate·FDA·Oct 29, 2026·Direct Rx

Sold nationwide. Longjili Trading is recalling about 50 Pamag Pieeoo twin-XL mattresses. The mattresses do not meet the mandatory federal flammability standard for mattresses, which can lead to serious injury or death from fire. No injuries have been reported.

Serious·CPSC·Oct 29, 2026·Longjili Trading

Sold nationwide. Harkla is recalling about 25,541 children's sensory compression swings in the U.S. because the ceiling hook can separate from its plate, posing a risk of serious fall injury. The company has received 29 reports of hook separation, including 14 injuries such as two concussions and a broken arm. The swings were sold online and in stores from March 2020 through December 2025.

Serious·CPSC·Oct 29, 2026·Harkla

Sold nationwide. Yinklev is recalling about 32,791 Jocoevol 6-drawer dressers sold on Amazon.com from December 2024 through July 2026 for about $160. The dressers can tip over if they are not anchored to the wall, posing risks of serious injury or death to children. They also do not meet a mandatory federal safety standard for clothing storage units.

Serious·CPSC·Oct 29, 2026·Yinklev

Sold nationwide. RootStim recalled about 11,000 minoxidil hair regrowth treatment bottles sold on Amazon from August 2025 through February 2026. The bottles are not child-resistant, which federal packaging rules require for minoxidil, so young children could open and swallow the product. No injuries have been reported.

Serious·CPSC·Oct 29, 2026·RootStim

Sold nationwide. HAIARA W5 PRO power banks sold on Amazon.com by Mitrytech are being recalled because the lithium battery can explode and ignite. The recall covers power banks with no date code printed on the side. About 11,000 units were sold for $18 to $22 from May 2025 through September 2026, and the company has received 600 reports of fire and other heat-related incidents, including three burn injuries.

Serious·CPSC·Oct 29, 2026·HAIARA

Sold nationwide. Bodum USA is recalling about 5.9 million French press coffee makers with replaceable glass carafes. The glass carafe can break during use, especially if it is cracked or damaged or if a metal spoon is used to stir the coffee. The company has received 70 reports of carafes breaking, including 48 reports of burns.

Serious·CPSC·Oct 29, 2026·Bodum

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