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The lithium-ion battery in the Super Off-Road 12,000 mAh Solar Wireless Power Bank can swell and overheat, creating a burn hazard. The company has received two reports of battery swelling. About 7,400 units were distributed as promotional items between January 2019 and December 2023.

Moderate·CPSC·Jun 25, 2026

The HeartMate 3 System Controller, which powers and monitors left ventricular assist devices (LVADs), may experience failures in its 11-volt backup battery. This backup battery is critical for emergency power when other power sources are unavailable.

Moderate·FDA·Jun 24, 20263 products

Merit Medical Systems' Splashwire Hydrophilic Guide Wire — used by doctors in vascular procedures — has been recalled because some product pouches were not sealed properly. Unsealed pouches can allow contamination or damage to the sterile device before use.

Moderate·FDA·Jun 24, 2026

Inspire Medical Systems is recalling two implant lead products, the Respiratory Sensing Lead and the Stimulation Lead, because they carry a Use By Date that goes beyond their validated three-year shelf life. The agency says material can degrade past the labeled date, which may lead to unplanned or premature revision surgery. No injuries have been reported.

Moderate·FDA·Jun 24, 2026·Inspire2 products

BD Connecta BD Luer-Lok 360 stopcocks used to administer IV fluids and medications may have a connection problem at Port C. When a plastic luer-lok syringe is attached, the connection may over-thread or continue spinning instead of tightening securely, making it feel unstable.

Moderate·FDA·Jun 24, 2026

A firmware bug in the iLet Bionic Pancreas can cause the lock screen to fail to unlock when users slide the unlock slider. When this happens, users become stuck on the lock screen and cannot change insulin cartridges or enter meal information. The pump will continue delivering insulin until the cartridge empties and the battery drains, which may lead to high blood sugar.

Moderate·FDA·Jun 24, 2026·Beta Bionics

Staar Surgical's ICL Calculation Software Version 8.00 contains a coding error that can produce incorrect implantation orientation diagrams for toric intraocular lenses. The error occurs when multiple toric lens calculations are generated for the same eye between April 13–16, 2026. An incorrect diagram could lead to improper lens alignment during surgery.

Moderate·FDA·Jun 24, 2026·Staar Surgical

Medline recalled 30 products, including urethral catheters, catheterization trays, intermittent latex catheters, and medical procedure kits. During an internal review, the company found that some samples did not meet performance specifications, including surface irregularities, connectors that detached early from the catheter funnel, and some catheters with outer diameters outside specification. No injuries have been reported.

Moderate·FDA·Jun 24, 202630 products

GE HealthCare is recalling three Giraffe OmniBed product lines, about 43,300 units in total, used as infant incubators and warmers. Under certain conditions, such as impact during transport, fasteners holding the canopy soffit beneath the control panel can come loose, and a fastener could fall into the patient compartment. In rare cases, the canopy soffit could become loose or detach, which could potentially injure a patient. No injuries have been reported.

Moderate·FDA·Jun 24, 20263 products

ConMed is recalling 11 AirSeal access port and obturator products used in minimally invasive (laparoscopic) surgery. The recall is for a potential problem that could cause overpressure alerts during procedures. No injuries have been reported, and the products were distributed nationwide and internationally.

Moderate·FDA·Jun 24, 2026·ConMed11 products

Stryker identified that some Triathlon Universal Baseplate Size 3 units (lot UZD9IB) were packaged in boxes labeled as Size 4, while Size 4 units (lot TYX7OB) were packaged in boxes labeled as Size 3. This labeling mix-up could result in using the wrong implant size during surgery.

Moderate·FDA·Jun 24, 20262 products

Accriva Diagnostics' directCHECK ACT-LR whole blood quality control product (level 2, lot A6DLA001) has incorrect performance range information on its label. This labeling error could lead to misinterpretation of test results if the correct reference range is not known.

Moderate·FDA·Jun 24, 2026

AMD Medicom is recalling two Ritmed neurological sponge products used during brain and spine surgery. The sponges may not consistently meet the limit for endotoxin, a bacterial substance, in devices that contact cerebrospinal fluid. No injuries have been reported.

Moderate·FDA·Jun 24, 2026·AMD Medicom2 products

Smith & Nephew identified a manufacturing error in certain TRIGEN Proximal Straight Humeral Nails (8/7 X 16, Ref: 71760816) in which the distal holes are missing. If implanted without detection, the affected nail could require revision surgery. Five units were distributed internationally.

Moderate·FDA·Jun 24, 2026·Smith & Nephew

Medtronic has identified a firmware anomaly in the O-arm O2 Imaging System detector panel that can cause image artifacts during surgical imaging. The issue affects specific serial numbers of the O-arm O2 model BI70002000. No injuries have been reported.

Moderate·FDA·Jun 24, 2026

Steris is recalling two surgical lighting systems, HarmonyAIR A-Series and ALYON, totaling about 2,650 units. The plus and minus buttons used to adjust light intensity on the light heads may detach. No injuries have been reported.

Moderate·FDA·Jun 24, 20262 products

Paint on the light heads of Steris HarmonyAIR A-Series Surgical Lighting Systems may chip or peel. This could potentially affect the lighting system's performance or introduce debris into the surgical field. The FDA has classified this as a Class II recall.

Moderate·FDA·Jun 24, 2026

Medline is recalling 34 convenience and procedure kits because they contain a recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. The adhesive's butyrate tubing may crack during use, making the product unusable for application. No injuries have been reported.

Moderate·FDA·Jun 24, 202634 products

Philips is recalling two imaging systems used in medical settings, the Allura Xper and MultiDiagnost Eleva, covering 2 product entries. The hand switch button may not fully release after use, which could cause loss of imaging function or unintended radiation exposure and extra contrast injection. No injuries have been reported.

Moderate·FDA·Jun 24, 20262 products

Dkiru LLC's Adndale Magnesium Glycinate Gummies 400 mg contain melatonin that is not listed on the label. The affected product is sold in 90-count plastic bottles (UPC 860008784551) with three affected lot numbers expiring between August and September 2026. Melatonin is a sleep aid not declared in the ingredient list, which poses a risk to consumers who may not expect it or who should avoid it due to other medications or health conditions.

Moderate·FDA·Jun 24, 2026

International Food Products is recalling three 50-pound bulk ingredient products after testing found Salmonella. They are Legacy Tex Dressing Stabilizer Blend #7604-50, Dairy House Ingredient Systems Vanilla Dairy Powder, and Dairy House Ingredient Systems Strawberry Dairy Powder 05#5072-50. About 658 bags were affected, and the products were shipped to Texas, Tennessee and Oklahoma. No illnesses have been reported.

Moderate·FDA·Jun 24, 20263 products

Fairhope Roasting Company Cold Brew Coffee Concentrate in 1-gallon jugs is missing a "Keep Refrigerated" statement on the label, even though the product requires refrigeration to stay safe. This labeling error could lead to improper storage and potential spoilage or foodborne illness. The affected batches were distributed to food service operations in Alabama.

Moderate·FDA·Jun 24, 2026·Fairhope Roasting Company

Great Value Hawaiian Roll 4-packs were found to have an oily and sticky substance on the food-contact surface of the packaging. The affected product was identified at wholesale distribution centers before reaching store shelves, and all units have been accounted for.

Moderate·FDA·Jun 24, 2026·Great Value

Nutrisystem Chocolate Cheesecake 2 oz frozen packages contain soy that is not declared on the label. People with a soy allergy who eat this product could have an allergic reaction. The recall affects 5,184 units with lot code CH030426 distributed across 25 states.

Moderate·FDA·Jun 24, 2026

Mid Dolciaria is recalling two cannoli products sold in boxes: Cannoli Siciliani (240g) and .155 Crunchy Cannoli Gluten Free (190g). The products contain chlorophyll E140 and E141, colorings that are not approved for use in these foods. No illnesses or injuries have been reported.

Moderate·FDA·Jun 24, 2026·Mid Dolciaria2 products

Dabur is recalling 14 antibiotic and antifungal creams, ointments and first aid products, including Lucky Super Soft, Circle K, Lil Drug Store, Rapidol, Cura Hongos and Med Pride. The FDA found manufacturing quality problems (CGMP deviations) during an inspection. No injuries have been reported.

Moderate·FDA·Jun 24, 2026·Dabur14 products

Inventia Healthcare Limited's chlorthalidone 25 mg tablets failed to meet dissolution specifications, meaning the tablets may not break down properly in the body and deliver the full dose. This affects 100-tablet and 1000-tablet bottles distributed nationwide. No injuries have been reported.

Moderate·FDA·Jun 24, 2026·Inventia Healthcare

Keystone Industries is recalling 7 topical anesthetic gels containing 20% benzocaine, sold as Pearson Quality, Quala, DHP, Burkhart, Dental City, PureLife, and safco SensiCaine-Ultra. The recall is due to a container defect: some bottles may have incomplete seals. No injuries have been reported.

Moderate·FDA·Jun 24, 2026·Keystone Industries7 products

Par Health USA's buprenorphine HCl injection (0.3 mg/mL) has been found to contain crystallization identified as buprenorphine free base in certain lots. This affects vials distributed nationwide. The FDA has classified this as a Class II recall.

Moderate·FDA·Jun 24, 2026

IntegraDose Compounding Services LLC is recalling Vasopressin 2 Units/2 mL syringes because the drug may contain less active ingredient than labeled. This affects two specific lots distributed nationwide. No injuries have been reported.

Moderate·FDA·Jun 24, 2026·IntegraDose