Colorado recalls

Sold nationwide. Little Giant ladders with Rapid Locks can suddenly retract if the locks are not fully engaged, which can cause a fall. The company received 25 reports of retraction, including 19 reports of injuries, three of them head injuries such as traumatic brain injury and skull fracture.

Serious·CPSC·Nov 5, 2026·Little Giant Ladder Systems

Sold nationwide. Arlopu slide playsets have openings where a child's torso can fit through but the head cannot, which may cause serious injury or death from entrapment. On model KT-CS17, the basketball nets can come unhooked from the rim and form a loop large enough for a child's head, which may cause entanglement or strangulation. Arlopu has received one report of an entrapment incident involving neck abrasions on a child.

Serious·CPSC·Nov 5, 2026·Arlopu

Sold nationwide. Bose is recalling lithium-ion battery packs sold for the S1 Pro and S1 Pro+ Bluetooth speaker systems. The battery packs can overheat and ignite, posing a risk of fire. The firm has received seven reports of battery packs melting, producing smoke or catching fire, including six reports of property damage, and no injuries have been reported.

Serious·CPSC·Nov 5, 2026·Bose

Sold nationwide. Intelerad has identified a cybersecurity vulnerability in IntelePACS software that could allow a malicious user to take over an administrator session, delete or modify image or study data, or lock legitimate users out. A separate software issue may cause unintended deletion of image data from an external archive integration.

Moderate·FDA·Nov 4, 2026·Intelerad

Sold nationwide. GE HealthCare found a nonconformance in certain Senographe Pristina VIA systems. In 3D+2D manual mode, when the anode track and filter combination is configured differently, the collimator blades might show in the image or the collimator might open more than expected, and the wrong collimator filter might be used for the selected anode track. This could deliver a minor additional X-ray dose to the patient and cause obvious image artifacts.

Moderate·FDA·Nov 4, 2026·GE3 products

Sold nationwide. Nalpac Ltd. is recalling DTF Sexual Chocolates. The product contains sildenafil and tadalafil, which are not listed on the label. The product was sold to about 16 customers, some with multiple stores, and 253 boxes are affected.

Serious·FDA·Nov 4, 2026·DTF

Sold nationwide. American Regent is recalling one lot of Cyanocobalamin Injection, USP, 1000 mcg/mL, in 25 x 1 mL multi-dose vials. The recall notice identifies the particulate matter in the product as glass. The product was distributed nationwide, and no injuries have been reported.

Moderate·FDA·Nov 4, 2026·American Regent

Sold nationwide. Corin Medical is recalling 22 Unity Knee ASC Modular Handles, part number 1232040, which are included in the Corin Unity ASC Instrument System. The locking mechanism may fail, so instruments already attached may not disengage and the handle may not fit securely onto unattached instruments. No injuries have been reported.

Moderate·FDA·Nov 3, 2026·Corin Medical

Sold nationwide. Remel, Inc. is recalling one lot of Yeastone Broth used in antibiotic susceptibility testing of mycological clinical specimens. The affected lot did not meet specifications and may report false susceptibility to Azole-family antifungal agents. No injuries have been reported.

Moderate·FDA·Nov 3, 2026·Remel

Sold nationwide. Baxter is recalling five surgical table and operating table column models: TruSystem 7500, TruSystem 7000 U, TS7500 MOBIUS, and TruSystem 7500 Hybrid Plus. The main lift may unexpectedly drop to its lowest position during use, and the tabletop could not be raised again after a drop. This has been linked to unexpected wear of the main lift assembly, also called the telescopic spindle. An uncontrolled drop may cause abrupt patient displacement, which could lead to traumatic injury, airway compromise, or surgical complications. Baxter has received three complaints and no patient injuries have been reported.

Serious·FDA·Nov 3, 2026·Baxter5 products

Sold nationwide. restor3d Inc. recalled certain Veritas Reverse Total Shoulder Replacement implants, sizes 1 and 2 with the 40 mm polymer liner. The FDA says this pairing may leave some polyethylene components without adequate retention strength, potentially causing dislocation, reduced range of motion, or revision surgery. No injuries have been reported.

Moderate·FDA·Nov 3, 2026·Restor3d

Sold nationwide. The recall covers 118 Shimadzu Trinias Opera Smart, Opera Grand and Smart OBL interventional fluoroscopic X-ray systems with C-arm support. The mounting bolts securing the C-arm drive unit may not be torqued to specification, potentially compromising structural stability and safe operation. No injuries have been reported.

Moderate·FDA·Nov 3, 2026·Shimadzu

Sold nationwide. Henry Schein is recalling 13 Perma Sharp surgical suture products, sold under Henry Schein and HSI item numbers, because the products lack 510(k) clearance from FDA. The recall covers U.S. nationwide distribution and shipments to Canada, Uganda, and the Cayman Islands. No injuries have been reported.

Moderate·FDA·Nov 3, 2026·Henry Schein13 products

Sold nationwide. Baxter is recalling two products: the TruSystem 7000 U Operating Table (dV), product code 1723633, and the mobile column TruSystem 7500 U, product code 1730720. The main lift may unexpectedly drop to its lowest position during use, and the tabletop may not be able to be raised again, which could cause abrupt patient displacement during surgery. The notice lists possible serious outcomes including traumatic injury and airway compromise. The products were distributed nationwide, with confirmed distribution in IL, MO and TX.

Serious·FDA·Nov 3, 2026·Baxter2 products

Sold nationwide. AVID Medical, Inc. is recalling Halyard MINOR PACK kits, model VASF105-08, because the header bags may have open seals, which could compromise sterility. The notice covers 108 kits. No injuries have been reported.

Moderate·FDA·Nov 3, 2026·AVID Medical

Sold nationwide. FDA analysis found undeclared sildenafil in Boner Bears Chocolate Syrup, which was sold to consumers through the firm's website. Sildenafil is not listed on the product label. No injuries have been reported.

Serious·FDA·Nov 3, 2026·Boner Bears

Sold nationwide. Fresenius Medical Care is recalling certain lots of DELFLEX Peritoneal Dialysis Solution with 1.5% Dextrose, 2,000 mL single-dose bags with an attached stay safe Exchange Set. Complaints reported potential leaks from small perforations in the print area of the primary bag, so the solution may not be sterile. No injuries have been reported.

Moderate·FDA·Nov 3, 2026·NxStage5 products

Sold nationwide. Hikma Pharmaceuticals USA Inc. is recalling 29,085 bottles of Ciprofloxacin Tablets, USP, 500 mg, 100-count. The FDA found N-nitroso-ciprofloxacin levels above its recommended interim control limit, a problem under current good manufacturing practice (CGMP) rules. No injuries have been reported.

Moderate·FDA·Nov 3, 2026·Hikma Pharmaceuticals2 products

Sold nationwide. Snack Right Super Foods, doing business as Brad's Raw Chips, is recalling certain Brad's kale chip products because they may contain thallium, a naturally occurring metal that kale can absorb from soil. The notice says high-level exposure can cause stomach illness, nerve damage and hair loss. The products were sold nationwide through KeHE and UNFI, with about 25,000 bags estimated in commerce.

Moderate·FDA·Nov 2, 2026·Brad's Raw Chips

Edwards Lifesciences is recalling 164 Commander M Delivery Systems, model 9880CM29A, from four lots. A manufacturing issue may cause the cardiovascular balloon to rupture. The notice reports no injuries.

Serious·FDA·Nov 2, 2026·Edwards Lifesciences

Sold nationwide. FDA classified this as a Class I recall of 11 Cardinal Health Presource PBDS kits, distributed in the US and Canada. Each kit contains BD Alaris Pump Infusion Sets for use with the BD Alaris Pump Module Model 8100, and the infusion sets were recalled for performance issues. The kits are labeled with names such as anesthesia, cath lab, C-section, labor, and emergency kits. No injuries have been reported.

Serious·FDA·Nov 2, 2026·Cardinal Health11 products

Sold nationwide. Vitality Works Inc. is recalling one lot of 365 Whole Foods Market Standardized + Full Spectrum Blend Ashwagandha Capsules (120 count) because it may be contaminated with Salmonella. The product was sold online at Amazon.com and at Whole Foods Market stores in several states and D.C. No illnesses have been reported.

Serious·FDA·Oct 30, 2026·Vitality Works

Sold nationwide. Once Upon A Farm is recalling all lots and varieties of its Tractor Wheels Organic Toddler Soft-Baked bars. The company says the bars can quickly turn into a dense, dry, sticky mass when they contact saliva and are chewed, which may pose a choking hazard for toddlers ages 1.5 to 2.5. The company reports three consumer complaints of choking and no injuries to date.

Serious·FDA·Oct 30, 2026·Once Upon A Farm

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