Delaware recalls

Sold nationwide. Boston Scientific is recalling 12 sizes of its CRE and CRE Pro Wireguided balloon catheters because the pouches they are packaged in may not keep the devices sterile. The recall covers 81,543 units per product and was distributed in the US and many other countries. No injuries have been reported.

Moderate·FDA·Jul 8, 2026·Boston Scientific12 products

Sold nationwide. The IntelliCuff portable cuff pressure controller may display a "Cuff System Leakage" error and cause the motor to pump continuously instead of maintaining the pressure set by the user. This can prevent the device from working as intended.

Moderate·FDA·Jul 8, 2026·Hamilton Medical AG

Sold nationwide. Certain lots of the Medtronic Harmony Delivery Catheter System may have a manufacturing defect that increases the risk of the distal tip detaching from the delivery system during use. This could occur under specific procedural or anatomical conditions. About 1,881 units worldwide are affected.

Serious·FDA·Jul 8, 2026·Medtronic Heart Valves Division

Sold nationwide. Remel, Inc. is recalling certain 100mm and 150mm GC Agar Base lab culture plates because some strains of gonorrhea bacteria may grow poorly or not at all on them. The recall covers specific lot numbers and was distributed in the US, Canada, Singapore, and the United Kingdom. No injuries have been reported.

Moderate·FDA·Jul 8, 2026·Remel

Sold nationwide. Windstone Medical Packaging is recalling four Aligned Medical Solutions surgical convenience kits, 1,525 units in total. The kits contain Webcol Large Alcohol Prep Pads that Cardinal Health recalled after a bacterium, Paenibacillus phoenicis, was found during a routine sterilization audit. The kits were distributed nationwide, with confirmed distribution in PA, GA, CA, and WA. No injuries have been reported.

Serious·FDA·Jul 8, 2026·Windstone Medical Packaging4 products

Sold nationwide. Medacta's Short Monobloc Stem Broaches (sizes 7–16), used during shoulder replacement surgery, have a manufacturing issue that causes the surgical instruments to be positioned slightly off-center during the procedure. This misalignment may increase the risk of fractures in the upper arm bone.

Moderate·FDA·Jul 8, 2026·Medacta Usa Inc

Sold nationwide. Certain lots of DePuy Synthes ATTUNE Revision Hinge Knee Insert components were found with external sterile packaging adhered to the internal sterile packaging. This contact may have compromised the sterility of the surgical implant inside.

Moderate·FDA·Jul 8, 2026·DEPUY (IRELAND)2 products

Sold nationwide. Specific lots of Medline reprocessed St. Jude Medical Response diagnostic electrophysiology catheters may contain small particles of residual material on surfaces that contact patients. If these particles dislodge during use, they could potentially cause blood clots, inflammation, or infection.

Serious·FDA·Jul 8, 2026·Medline

Sold nationwide. Medline is recalling 8 convenience kits that contain Swan-Ganz catheters made by Becton Dickinson (BD). BD received complaints that the blue hub on these catheters can leak or break, which may lead to infection, medication loss, or blood loss. No injuries have been reported, and the kits were distributed in AZ, CA, FL, IL, MO, NJ, OH, OK, TN, TX, and WI.

Moderate·FDA·Jul 8, 2026·Medline8 products

Sold nationwide. Insulet is recalling three Omnipod pod lines (Omnipod 5, Omnipod DASH, and Omnipod Eros), about 7 million units in total. Damage to the soft cannula during manufacturing can let insulin leak around the pod instead of being delivered, so users may get too little insulin. This can cause high blood sugar, and in severe cases prolonged high blood sugar can lead to diabetic ketoacidosis, hyperglycemic hyperosmolar syndrome, or death. No injuries have been reported.

Serious·FDA·Jul 8, 2026·Insulet3 products

Sold nationwide. Four Hillrom VOLARA System patient circuit kits are included in this recall. Air and medication can leak from the nebulizer cup during therapy, which can lower a patient's oxygen level and make the treatment less effective. The problem has been linked to the nebulizer cup not being locked properly after medication is added during setup. No injuries have been reported.

Serious·FDA·Jul 8, 2026·Baxter4 products

Sold nationwide. Medline is recalling 15 convenience kits that contain Huons lidocaine ampules. Huons issued the recall after an FDA inspection of its manufacturing site found quality problems with the ampules. No injuries have been reported.

Moderate·FDA·Jul 8, 2026·Medline15 products

Sold nationwide. Certain coaxial breathing circuit sets used with Hamilton Medical ventilators (models C1, T1, and MR1) may have expiratory valve membranes that stick to the valve body. This defect is not always detectable before use and can trigger an "exhalation obstructed" alarm during ventilation, potentially leading to inadequate ventilation and oxygen desaturation in patients.

Serious·FDA·Jul 8, 2026·Hamilton Medical AG

Sold nationwide. Nara Organics Whole Milk Organic Infant Formula in two sizes may be contaminated with Clostridium botulinum, a bacterium that can cause botulism. The contamination was identified in specific lot codes with use-by dates between March 2027 and February 2028. No illnesses have been reported.

Serious·FDA·Jul 8, 2026·nara organics

Sold nationwide. PH Labs is recalling two dietary supplements, Ocular Plus and Vista MAX, because they contain Yellow No. 5 dye that is not listed on the label. Ocular Plus was distributed by L.A. Farmacia Natural and Vista MAX by Vision of Health, with about 6,967 units of each affected. The products went to two local retail stores, and no injuries have been reported.

Moderate·FDA·Jul 8, 2026·PH Labs2 products

Sold nationwide. MOGO Pure Moringa Oleifera capsules may be contaminated with Salmonella Typhimurium. The contamination was discovered during testing. Affected bottles were sold online through Amazon, eBay, Etsy, and mogomiranga.com.

Serious·FDA·Jul 8, 2026·MOGO

Sold nationwide. Cipla USA is recalling specific lots of Cinacalcet Hydrochloride 30 mg tablets because they contain elevated levels of N-nitroso-cinacalcet, a manufacturing impurity that exceeds FDA safety limits. The affected bottles were distributed nationwide.

Moderate·FDA·Jul 8, 2026·Cipla3 products

Sold nationwide. Lannett Company distributed amphetamine extended-release capsules that contained only immediate-release pellets but were labeled as extended-release. This labeling error could result in incorrect dosing and medication timing for patients who depend on the extended-release formulation.

Moderate·FDA·Jul 8, 2026·Lannett

Sold nationwide. Asclemed USA Inc. is recalling two lidocaine HCl 1% injection products in 5 mL single-dose ampules, sold nationwide. One is sold as Accucaine kits and the other is an unbranded lidocaine injection; both were distributed by Enovachem Pharmaceuticals. The recall was issued because the products may not be sterile, and no injuries have been reported.

Moderate·FDA·Jul 8, 2026·Asclemed USA Inc.2 products

Sold nationwide. Accord Healthcare is recalling one lot of levothyroxine sodium 300 mcg tablets because they may contain less active ingredient than labeled. This means the medication may not work as intended for patients who need it to manage thyroid conditions.

Moderate·FDA·Jul 8, 2026·Accord Healthcare

Sold nationwide. Lupin Pharmaceuticals is recalling multiple lots of prednisolone acetate ophthalmic suspension 1% (an anti-inflammatory eye drop) due to the presence of a foreign substance in some bottles. The affected lots were distributed nationwide. No injuries have been reported.

Moderate·FDA·Jul 8, 2026·Lupin

Sold nationwide. Accord BioPharma is recalling one lot of IMULDOSA (ustekinumab-srlf) injection due to lack of assurance that the product is sterile. The affected lot may not meet sterility standards required for injectable medications. No injuries have been reported.

Moderate·FDA·Jul 8, 2026·ACCORD BIOPHARMA INC

Sold nationwide. CareFusion is recalling 10 antiseptic skin prep products sold as BD ChloraPrep (Hi-Lite Orange, Clear and Scrub Teal), BD PurPrep, and ChloraPrep FREPP. Applicators that were meant to be sterilized before use were instead shipped to customers outside the intended distribution channel, so they may not be sterile. No injuries have been reported.

Moderate·FDA·Jul 8, 2026·CareFusion10 products

Sold nationwide. Lupin Pharmaceuticals is recalling certain lots of its Glucagon Emergency Kit because the syringe plunger may not move smoothly during use. This defect was discovered during stability testing and could prevent the kit from working properly in an emergency.

Moderate·FDA·Jul 8, 2026·Lupin

Sold nationwide. Mars Petcare discovered that two lots of Pedigree High Protein Chopped Chicken & Duck Flavor wet dog food were fraudulently diverted into stores after being sent for destruction due to quality concerns. The affected cans may contain pieces of sharp metal and plastic that could harm dogs if eaten.

Serious·FDA·Jul 3, 2026·Pedigree

Sold nationwide. Winco Fireworks International is recalling Roman Candles 8 Shot fireworks (Model RCLR-W8012) because they can malfunction. During use, shots may blow out the side of the tube instead of firing normally, creating a risk of serious injury from explosions and burns.

Serious·CPSC·Jul 2, 2026·Winco Fireworks

Sold nationwide. Winco Fireworks International is recalling Unity 7 Shot 200 Gram Aerial Cake fireworks (model MEF6096) because they can tip over during use, creating a risk of serious injury from explosion and burns. The affected fireworks were sold in red, white and blue packaging at Pyro City and independent fireworks retailers nationwide between January and May 2026.

Serious·CPSC·Jul 2, 2026·Winco Fireworks

Sold nationwide. Small metal wire bristles can detach from Cuisinart grill brushes during use and stick to food or the grill. If swallowed, these bristles can cause serious internal injuries requiring surgery. Conair has received 54 reports of detached bristles, including 3 cases where consumers needed medical treatment to remove bristles from their throat or digestive tract.

Serious·CPSC·Jul 2, 2026·Conair

Sold nationwide. Junpower CR2032 lithium coin batteries sold on Amazon lack the child-resistant packaging and warning labels required by federal law. If swallowed, these batteries can cause serious internal injuries or death. About 67,000 units were sold between December 2023 and September 2024.

Serious·CPSC·Jul 2, 2026·JSNJ_Tech

Sold nationwide. The LED board inside Metalux Optimized High Bay light fixtures can overheat or contact the lens and nearby combustible materials, creating a fire hazard. The company has received nine reports of these fixtures catching fire. About 42,000 fixtures sold since April 2020 are affected.

Serious·CPSC·Jul 2, 2026·Cooper Lighting