Minnesota recalls

BabyBond retractable safety gates can allow a child's torso to fit through the gap between the gate and floor, creating a serious entrapment risk. The gates were sold at Target.com between November 2024 and October 2025. No injuries have been reported, but the hazard poses a risk of serious injury or death.

Pieces inside DR Power leaf vacuums can come loose or debris can pierce the chute, causing material to shoot out and potentially cut users or bystanders. The company has received 46 reports of debris being ejected, though no injuries have been reported yet.

Agrish adult portable bed rails (models 2512, 2513, and 2516) can trap users between the rail and mattress, creating a serious risk of entrapment and suffocation. The rails do not meet federal safety standards. About 5,000 units were sold on Amazon between April and October 2025.

Beaver-Visitec International's BVI Leos Laser and Endoscopy System (Model OME6000U) has a manufacturing defect in the USB cable that connects the Nurse Monitor touchscreen to the System Controller. The cable is missing required ferrite components that protect against electromagnetic interference. Five units with specific serial numbers were affected and distributed in Florida, Michigan, Oklahoma, Texas, and Wisconsin.

Philips EPIQ Ultrasound Systems with the X5-1c transducer and certain software versions may unexpectedly restart on their own. This automatic reboot can damage the transducer. No injuries have been reported.

Sheathes3D Seamless Viral Barrier ultrasound probe covers may have manufacturing defects that could allow contamination during medical use. This poses a risk of infection to patients. The recall affects a limited quantity distributed in Washington State.

Ferndale Laboratories is recalling Mastisol Liquid Adhesive (lot 24161B, expiration 10-31-2029) because the butyrate tube can crack when you try to use it, making the product unusable. This affects 24,589 vials distributed in the US and UK.

Some units of the Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe (catalog VS0135.25, lot 2509040) may not fit smoothly through a 25-gauge cannula as intended. This could affect proper use during medical procedures. The recall affects 221 units distributed in the US and Japan.

Atomstack material processing laser products lack a required remote interlock connector that is designed to shut down the laser if the protective enclosure is opened. This safety feature is mandated by federal laser safety regulations to prevent accidental exposure.

Tom Bumble LLC is recalling Nutty Peanut Butter Flake Candy bars because they may contain foreign material. The affected products have Best By dates between May 21, 2026 and June 9, 2026. No injuries have been reported.

Bendon Inc. is recalling several heart-shaped and character-themed gummy candy products because they contain chlorophyllin copper complex, a color additive that is not approved for use in food in the United States. The affected products include Paw Patrol, Mickey Mouse, Stitch, SpongeBob, and Toy Story gummies with best-before dates of 08/19/2027. No injuries have been reported.

Zydus Pharmaceuticals is recalling certain bottles of trazodone 100mg tablets because some tablets have dents on the surface. The defect affects lot EA00237A with an expiration date of 04/30/2027. No injuries have been reported.

Glenmark Pharmaceuticals discovered that blister packs containing Ondansetron 4mg orally disintegrating tablets are not fully sealed, allowing tablets to fall out. The affected product was repackaged and distributed nationwide. This applies to lot #19251311 with an expiration date of April 2027.

Novo Nordisk has recalled specific batches of Wegovy (semaglutide) 1 mg injection pens because hair was found inside prefilled syringes. This affects two lot numbers distributed nationwide. No injuries have been reported.

Novo Nordisk discovered hair in some prefilled Wegovy injection pens. This affects specific lot numbers manufactured in Denmark. No injuries have been reported.

CareFusion 213, LLC is recalling BD ChloraPrep Triple Swabsticks (a skin antiseptic swab) because the manufacturer cannot confirm the product was properly sterilized. The affected lot (#5086623, expiring 3/31/2028) was distributed nationwide. No injuries have been reported.

Beckman Coulter Bicarbonate Reagent (catalog numbers OSR6137, OSR6237, OSR6637) used in laboratory analyzers may produce falsely high bicarbonate test results. This happens because a substance in blood samples called Lactate Dehydrogenase (LDH) interferes with the test. Affected lot numbers are listed in specific ranges for each catalog number.

A software problem in the Medtronic Restore Clinician Programmer App (versions before v.1.0.4489) can cause a Device Reset message that cannot be cleared. In rare cases, this prevents the pain management device from resuming therapy, causing patients to experience pain symptoms again. The implanted devices themselves are not affected—only the programmer application used by clinicians.

Cook Medical recalled Rösch-Uchida Transjugular Liver Access Sets (part number RUPS-100) used in liver procedures because some units were manufactured incorrectly. Affected devices may have been cut to the wrong length, not properly trimmed, or not inspected. Only 23 units were affected worldwide.

Cook Medical found that certain Ring Transjugular Intrahepatic Access Sets used in liver procedures were manufactured incorrectly. Affected devices may have been cut to the wrong length, trimmed improperly, or not inspected properly before shipment. This involves 15 units distributed worldwide.

Cook Medical recalled certain Flexor Check-Flo Introducer and Set models because some units were manufactured out of specification. Affected devices may have been cut to incorrect lengths, not properly trimmed, or not inspected properly. This is a medical device used in vascular procedures.

Diasol has recalled a bicarbonate dialysis liquid concentrate (product 100425-10-DEX100, lot PHV08042) because the FDA cannot confirm it is safe and effective for use. The recall affects approximately 2,200 gallons distributed across Missouri, California, Arizona, Texas, Illinois, and Massachusetts.

Safety and efficacy of dialysis acid concentrate cannot be assured

Diasol, Inc. is recalling specific lots of its 100230-10-DEX100 bicarbonate dialysis liquid concentrate because the safety and efficacy of the product cannot be assured. The affected product was distributed nationwide in Missouri, California, Arizona, Texas, Illinois, and Massachusetts. No injuries have been reported.

Diasol, Inc. is recalling a dialysis acid concentrate product because the safety and efficacy of the product cannot be assured. The recall affects 4,400 gallons of product distributed nationwide to medical facilities in Missouri, California, Arizona, Texas, Illinois, and Massachusetts.

Diasol has recalled specific lots of its liquid concentrate used in bicarbonate dialysis machines. The FDA determined that the safety and efficacy of this product cannot be assured. The recall affects 7,200 gallons distributed across six states.

Diasol is recalling specific lots of its bicarbonate dialysis liquid concentrate because the safety and efficacy of the product cannot be assured. The affected product was distributed nationwide to dialysis facilities in Missouri, California, Arizona, Texas, Illinois, and Massachusetts. No injuries have been reported.

Microbiologics Inc. is recalling certain LYFO DISK products containing Campylobacter jejuni subsp. jejuni (Catalog Number 0325L) because affected units may fail to recover the target microorganism as intended. This affects laboratory testing and quality control processes.

Microbiologics Inc. recalled certain KWIK-STIK 6-Pack bacterial culture products (Catalog Number 0325K) because affected units may fail to properly recover the target microorganism Campylobacter jejuni subsp. jejuni. This means laboratory and testing professionals using these products may not be able to verify that the cultures are viable or suitable for their intended testing purposes.

Microbiologics Inc. has recalled specific lots of KWIK-STIK 2-Pack test kits used to detect Campylobacter jejuni bacteria. The affected units may fail to correctly recover the target microorganism, which could lead to false negative test results in laboratory testing.