Delaware recalls

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

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

Sold nationwide. CooCooBaby Classic and Deluxe Baby Loungers have design flaws that create unsafe sleeping conditions for infants. The sides are too short to keep a baby secure, the sleeping pad is too thick and can cause suffocation, and babies can fall out or get trapped at the foot opening.

Serious·CPSC·Jun 18, 2026·CooCooBaby

Sold nationwide. Joolz Aer2 Car Seat Adapters can fail to attach properly to Joolz Aer2 strollers, allowing the car seat to fall. The company has received one report of the adapters detaching. No injuries have been reported so far.

Serious·CPSC·Jun 18, 2026·Joolz

Sold nationwide. SHEIN Distribution Corporation is recalling Michley-branded children's pajamas sold online because they don't meet mandatory flammability standards for sleepwear. The recalled one-piece pajamas came in green, pink, yellow, and purple with animal patches, in sizes 80–130. They pose a risk of serious burn injuries.

Serious·CPSC·Jun 18, 2026·Shein

Sold nationwide. Arizer Solo III portable vaporizers with certain serial numbers contain a defective lithium-ion battery that can overheat, explode, or ignite, posing a serious fire and burn risk. The company has received four reports of batteries exploding or catching fire. About 5,000 units sold between May 2025 and January 2026 are affected.

Serious·CPSC·Jun 18, 2026·Arizer Tech

Sold nationwide. Veseacky children's pajama sets sold on Amazon do not meet mandatory federal safety standards for sleepwear and pose a risk of serious burns to children. The sets consist of a long-sleeve button-up top and matching pants, sold in various colors and prints from October 2020 through January 2026.

Serious·CPSC·Jun 18, 2026·Veseacky

Sold nationwide. Arrogantf white spa and hot tub drain covers do not meet federal safety standards for entrapment protection. They pose a risk of serious injury or death from entrapment and drowning, particularly to children. About 340 units were sold online through Amazon between September 2025 and March 2026.

Serious·CPSC·Jun 18, 2026·Arrogantf

Sold nationwide. GOPO Toys pull string teething toys have silicone strings that are longer and thinner than safety standards allow. The strings can reach the back of a child's throat and become lodged, causing choking or respiratory distress. The company has received three reports of strings reaching children's throats.

Serious·CPSC·Jun 18, 2026·GOPO Toys

Sold nationwide. BABESIDE toy sets sold on Amazon contain small parts that pose a choking risk to children under 3: a pacifier and a plush bear with detachable eyes. These pieces are not safe for young children and violate federal small parts rules.

Serious·CPSC·Jun 18, 2026·Huitong Crafts

Sold nationwide. Boston Scientific is removing Orca Sterile Single Use Air/Water and Suction Valves from distribution because the suction button is sticking more often than expected. These valves are used during gastrointestinal endoscopic procedures to control air and water flow on endoscopes. No injuries have been reported.

Moderate·FDA·Jun 17, 2026·Boston Scientific

Sold nationwide. AVID Medical is recalling four Halyard kit types because sealed pouches were distributed without validated sterilization. The kits may not be sterile, and the recall includes 476 kits total, distributed in Iowa. No injuries have been reported.

Moderate·FDA·Jun 17, 2026·AVID Medical4 products

Sold nationwide. Elekta's MOSAIQ Oncology Information System software (version 3.2) may fail to load an adapted baseline shift plan during cancer treatment delivery if a communication error occurs. This could affect the accuracy of radiation therapy positioning. No injuries have been reported.

Moderate·FDA·Jun 17, 2026·Elekta

Sold nationwide. Abbott's Merlin PCS 3650 programmer software (versions 25.0.1 through 28.7.1) may malfunction during pacing capture threshold tests on pacemakers. When this occurs, the programmer may fail to successfully send the command to stop the test.

Moderate·FDA·Jun 17, 2026·Abbott

Sold nationwide. Boston Scientific is recalling the Model SC-4318 Clik X Anchor (Lot #35107836) because sterile anchors may lack proper sterility assurance. Approximately 43 units were distributed across six U.S. states.

Moderate·FDA·Jun 17, 2026·Boston Scientific

Sold nationwide. Boston Scientific is recalling two lines of reusable electrodes, CSK and TCN, because they may not meet expected performance levels. The recall covers 2 products with about 81,000 units total, distributed across the US and several other countries. No injuries have been reported.

Moderate·FDA·Jun 17, 2026·Boston Scientific2 products

Sold nationwide. Some units of Inter-Med's Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit (catalog 504600-28) contain the package insert for Ferric Sulfate Gel instead. The wrong insert gives incorrect first aid instructions—specifically, it tells users to induce vomiting if the gel is swallowed, when the correct instructions say not to induce vomiting.

Moderate·FDA·Jun 17, 2026·Inter-Med