Alaska recalls

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·BD

Sold nationwide. 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

Sold nationwide. 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

Sold nationwide. 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, 2026·Medline30 products

Sold nationwide. The Mito Red Light Super Mobile near-infrared therapy device contains a lithium-ion battery that may malfunction and catch fire or burst into flames. The device has been distributed worldwide, including across the United States.

Serious·FDA·Jun 24, 2026·Mito Red Light

Sold nationwide. 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, 2026·GE3 products

Sold nationwide. 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

Sold nationwide. 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, 2026·Howmedica Osteonics2 products

Sold nationwide. 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·Accriva Diagnostics

Sold nationwide. 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·Medtronic

Sold nationwide. 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, 2026·Steris2 products

Sold nationwide. 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·Steris

Sold nationwide. 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, 2026·Medline34 products

Sold nationwide. 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, 2026·Philips2 products

Sold nationwide. Arrow is recalling 35 kits and sets that contain lidocaine, bupivacaine, or 0.9% sodium chloride from a supplier that was itself recalled for quality issues. If the sterility of these water-based injectable drugs is compromised, it could lead to serious or life-threatening injuries. No injuries have been reported, and the products were distributed nationwide.

Serious·FDA·Jun 24, 2026·Arrow35 products

Sold nationwide. A software error in certain Automated Impella Controller devices (used to manage left heart support blood pumps) may affect device function. The error affects controllers with software versions 6.0.1, 6.0.2, 6.0.3, 7.1 and above across multiple regions worldwide.

Serious·FDA·Jun 24, 2026·Abiomed

Sold nationwide. Datex-Ohmeda is recalling three infant resuscitation and warmer products, 550 units in total, because a blender knob shaft can loosen. This can cause the system to deliver an oxygen concentration that differs from the level set by the user, which could lead to too little or too much oxygen for the patient. Only units with a specific blender installed during service are affected.

Serious·FDA·Jun 24, 2026·Datex-Ohmeda3 products

Sold nationwide. 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·Adndale

Azuma Foods Tako Wasabi seasoned octopus contains fish that is not declared on the label. People with fish allergies could have a serious allergic reaction if they eat this product. The recall affects frozen retail packs and foodservice units distributed across multiple states.

Serious·FDA·Jun 24, 2026·azuma foods

Sold nationwide. 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

Sold nationwide. 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

Sold nationwide. 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

Sold nationwide. Sandoz is recalling one lot of Focalin XR (dexmethylphenidate HCl) 5 mg extended-release capsules because some bottles have incorrect or missing lot numbers and expiration dates on the label. The affected lot (VA0099422) was distributed nationwide. This is a labeling issue only; the medication itself has not been found to be unsafe.

FDA·Jun 24, 2026·Sandoz

Sold nationwide. 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

Sold nationwide. 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·Paragon 28

Sold nationwide. Ajanta Pharma USA Inc. distributed bottles labeled as Aripiprazole 30 mg that actually contained Voriconazole 50 mg, a different medication used to treat fungal infections. This mix-up affected 6,143 bottles (Lot PA00805, expiring 01/31/2029) distributed nationwide. The error was discovered and reported to the FDA.

Serious·FDA·Jun 24, 2026·Ajanta Pharma

Sold nationwide. 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

Sold nationwide. VistaPharm is recalling four sizes of Kerr Insta-Char activated charcoal with cherry flavor, in aqueous and sorbitol bases. The product did not meet the FDA over-the-counter monograph M023 standard. No injuries have been reported.

Moderate·FDA·Jun 24, 2026·Pain Train Salsa4 products

Sold nationwide. Glenmark Pharmaceuticals is recalling specific lots of Alyacen 7/7/7 (a birth control pill) because testing found higher-than-allowed impurity levels in the tablets. The affected lots were distributed nationwide. No injuries have been reported.

Moderate·FDA·Jun 24, 2026·Glenmark

Sold nationwide. MorningStar Farms is recalling two products because they may contain plastic pieces. The affected items are Buffalo Chik'n Nuggets (10.5 oz) and Hot & Spicy Sausage Patties (8 oz) with specific "Better if Used Before" dates in early July 2027.

Moderate·FDA·Jun 18, 2026·Morningstar Farms