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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, 20264 products

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

DePuy (Ireland) is recalling 2 ATTUNE Revision Hinge knee components, a housing component and an insert component, because the outer sterile packaging was found stuck to the inner sterile packaging, which could compromise sterility. The recall covers 226 units distributed to Minnesota, North Carolina, and Texas. No injuries have been reported.

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

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

A single lot of 10cc Luer Lok syringes (Lot 8298877) with an expiration date that had passed were distributed to hospitals and medical facilities in California, Florida, and Pennsylvania due to a failure in the distribution system's inventory controls. About 1,401 syringes were affected. No injuries have been reported.

Moderate·FDA·Jul 8, 2026·Mentor

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, 20268 products

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

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, 202615 products

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

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

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, 20263 products

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

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

Boehringer Ingelheim Pharmaceuticals is recalling one lot of Synjardy XR 12.5/1000 mg tablets due to manufacturing quality control issues. During production, an incorrect cleaning agent was used on equipment, and required testing of that equipment was not completed before the tablets were made.

Moderate·FDA·Jul 8, 2026·Boehringer Ingelheim

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

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

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

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, 202610 products

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

Kao USA recalled select lots of Oribe Serene Scalp Densifying Shampoo (8.5 oz and 33.8 oz) made between February 21–26, 2026 after detecting Pluralibacter gergoviae bacteria. People with weakened immune systems may be at higher risk of infection.

Moderate·FDA·Jul 1, 2026·Kao

Abiomed is recalling four Impella CP product sets that include 14 Fr Low Profile Introducer Kits, with 195 affected units in total. The introducer may form blood clots (thrombus) during prolonged use. No injuries have been reported, and the distribution covers the US states of FL, IL, MN, NJ, NY, and VA, plus Japan.

Serious·FDA·Jul 1, 20264 products

Medline is recalling 16 convenience kits that contain 10mL polycarbonate colored syringes. The company found design changes to these kits that were not cleared by the FDA, and the products were not included in an earlier report. The kits were shipped nationwide and to Barbados, and no injuries have been reported.

Moderate·FDA·Jul 1, 202616 products

Boston Scientific has recalled one INTERA 3000 Hepatic Artery Infusion Pump (model AP-0300H) due to the potential for leakage along the drug pathway from the pump through the catheter end. This is an implantable device used to deliver medication directly to the liver. The affected device was distributed in Ohio.

Moderate·FDA·Jul 1, 2026

Philips Telemetry Monitor 5500 (model 867232) devices may unexpectedly reset to a default state, causing them to lose their configuration settings and disconnect from the hospital's central monitoring system. This could prevent the monitor from reconnecting to the PIC iX central system until manually reconfigured.

Moderate·FDA·Jul 1, 2026

Zimmer discovered that 12 units of the Persona Revision Trabecular Metal Femoral Distal Augment (Model 42-5572-066-10, Size 9/9+, 10mm thickness) contained an incorrect posterior augment component in the package instead of the correct distal augment. No patient injuries have been reported.

Moderate·FDA·Jul 1, 2026

Medtronic recalled three models of its Octopus tissue stabilizers, covering 1,012 units in total. During manufacturing, the company found that the tubing was attached backwards, with the short tube on the bottom of the canister and the long tube on top. No injuries have been reported.

Moderate·FDA·Jul 1, 20263 products

Certain lots of Dexcom G7 continuous glucose monitoring sensors that were designated for destruction were stolen and later sold to pharmacies and distributors without authorization. Two affected lots have different risks: one was not properly sterilized and poses an infection risk, and the other may not provide accurate readings or detect dangerous blood sugar levels.

Moderate·FDA·Jul 1, 2026

Surgify Medical is recalling 19 Surgify Halo drill burr products used in bi-portal endoscopic spinal surgery because the burrs may break during use. The recall was filed as a Class II device recall, and no injuries have been reported. The products were distributed nationwide, including to MN, MA, IN, LA, CA, NY, and FL.

Moderate·FDA·Jul 1, 2026·Surgify Medical19 products

A software issue in the Thuvera Laser Console (Software Version 2.2) causes the device to display a false error code 5018. This anomaly may lead clinicians to misinterpret the device status during operation.

Moderate·FDA·Jul 1, 2026·IPG Medical

GE Healthcare's AW Server 3.2 ext.6.5 has a software issue that can cause the system to display a previous patient's medical images instead of the correct patient's images when launching certain applications. There is no warning or error message when this happens. If a radiologist or clinician does not notice the error, they could misread images, make wrong diagnoses, or recommend incorrect treatment.

Moderate·FDA·Jul 1, 2026