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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

Stryker Neurovascular's INZONE Detachment System devices may experience premature battery drain, causing them to fail to power on, display faint indicators, or be unable to detach an embolization coil as intended. If a device fails during a procedure, medical staff may need to use an alternative technique to complete the intervention.

Moderate·FDA·Jul 1, 2026

Acumed Hexalob Screws used in wrist fixation systems may break during use due to a manufacturing error. The affected screws come in various sizes (2.7mm and 3.0mm) and have been distributed nationwide. No injuries have been reported.

Moderate·FDA·Jul 1, 2026·Acumed

Zimmer Biomet is recalling five Off-Axis shoulder system reamer guide products distributed nationwide. The company received five complaints that the plastic guides caught during reaming and broke. No injuries have been reported.

Moderate·FDA·Jul 1, 20265 products

PFM Medical's Multi-Snare Set catheters (5 mm and 10 mm models) failed to meet biocompatibility safety standards. If used, the device material could cause localized inflammation and tissue irritation when in contact with blood vessels.

Moderate·FDA·Jul 1, 2026·PFM Medical

TMJ Solutions Inc. has recalled one custom temporomandibular joint implant (model CHG020) that may contain incorrect patient-specific components. The mismatch caused a poor fit, resulting in a right-sided open bite for the affected patient.

Moderate·FDA·Jul 1, 2026·TMJ Solutions

Philips is recalling two Avalon fetal monitor models, the FM20 and FM30, because the speaker connector may have been assembled incorrectly. Device cables can be pulled out of the housing, which may cause intermittent or permanent loss of speaker output. The recall includes 454 affected units, and no injuries have been reported.

Moderate·FDA·Jul 1, 20262 products

Boichik Bagels is recalling three products sold in California: whitefish salad, tuna salad, and pumpernickel mix bagels (6 per package). The salads list eggs in their ingredients, but eggs are missing from the allergen "contains" statement on the labels. No illnesses have been reported.

Moderate·FDA·Jul 1, 20263 products

Produce Innovations roast beef and Swiss closed-face sandwiches were labeled as turkey and cheddar. The mislabeling could expose people with allergies or dietary restrictions to ingredients they were not expecting. This affects 112 units distributed to medical facilities and vending machines in Illinois, Iowa, Kansas, and Missouri.

Moderate·FDA·Jul 1, 2026

El David Gelee Bonbons with fruits (400g boxes) contain two food dyes—FD&C Yellow 5 and FD&C Red 40—that are not listed on the package label. People with allergies or sensitivities to these dyes could have a reaction if they eat the product without knowing the dyes are present.

Moderate·FDA·Jul 1, 2026

Motor City Pizza Co. 5 Cheese Bread products may contain Salmonella, a bacteria that can cause serious illness. The affected products were distributed nationwide to major retailers including Costco, Walmart, Target, and Kroger.

Moderate·FDA·Jul 1, 2026

Joy Gourmet Foods is recalling 14 flavors of lassi, a yogurt-based drink, because the products may not have been adequately pasteurized. The flavors include Mango, Rose, Sweet, Salty, Pineapple, Strawberry, Mango-Pina-Strawberry, Mango-Pina-Orange, Plain Chaash, Masala Chaash, Mint, Peach, Orange and Saffron Cardamon, sold in 16 oz. and some 64 oz. sizes. The recall covers products distributed in New York, New Jersey and Pennsylvania, and no illnesses have been reported.

Moderate·FDA·Jul 1, 2026·Joy14 products

Sun Pharmaceutical discovered that some bottles labeled as containing 6mg Perampanel tablets actually contained 10mg tablets instead. This mix-up affects one lot (AE01763) distributed nationwide. Patients taking the wrong strength could receive an incorrect dose of this seizure medication.

Moderate·FDA·Jul 1, 2026

Elevate Oral Care's Povi-One 10% Povidone-Iodine Oral Antiseptic does not contain the full strength stated on the label. Five specific production lots distributed nationwide do not meet the required potency standard, which means the product may not work as intended for oral antiseptic purposes.

Moderate·FDA·Jul 1, 2026·Elevate Oral Care

Some bottles of Lacosamide 100mg tablets may contain Selexipag 1000 mcg tablets instead. This mix-up happened during manufacturing and could cause patients to take the wrong medication. The recall affects specific lots distributed nationwide.

Moderate·FDA·Jul 1, 2026·Annora Pharma

CareFusion is recalling four sizes of BD ChloraPrep Clear and BD ChloraPrep FREPP Clear skin antiseptic applicators because wrinkles in the paper lid may break the seal, so the products may not stay sterile. No injuries have been reported. The products were distributed nationwide in the U.S. and to other countries.

Moderate·FDA·Jul 1, 20264 products

PReye LLC is recalling all lots of PReye Vitamin See Antioxidant Preservative Free Eye Drops due to lack of assurance of sterility. The recall affects approximately 50 to 60 bottles distributed in Colorado. No injuries have been reported.

Moderate·FDA·Jul 1, 2026·PReye

ANI Pharmaceuticals is recalling hydroxyzine hydrochloride oral solution (10 mg/5 mL, 473 mL bottles) due to the presence of a foreign substance in one lot. The affected product was distributed nationwide. No injuries have been reported.

Moderate·FDA·Jul 1, 2026·ANI Pharmaceuticals

Central Admixture Pharmacy Services issued a recall for one patient-specific Total Parenteral Nutrition (TPN) bag that did not contain copper and famotidine as listed on the label. The bag was prepared for a pediatric patient in Massachusetts. No injuries have been reported.

Moderate·FDA·Jul 1, 2026·Central Admixture Pharmacy Services

Direct Rx's packaged Duloxetine D/R 30 mg capsules contain levels of N-nitroso-duloxetine, a potentially harmful impurity, above FDA's recommended limit. This is a manufacturing quality issue affecting specific lots distributed nationwide.

Moderate·FDA·Jul 1, 2026·Direct Rx

Amgen is recalling five bottle sizes of two prescription heart and thyroid-related drugs, Corlanor (ivabradine) and Sensipar (cinacalcet), because the tablets may contain a foreign substance. The products were distributed nationwide, and no injuries have been reported.

Moderate·FDA·Jul 1, 2026·Amgen5 products

Ajanta Pharma USA Inc. is recalling one lot of fenofibrate 200 mg capsules due to manufacturing quality deviations discovered during inspection. The affected lot (PA02216, expiring 12/2029) was distributed nationwide.

Moderate·FDA·Jul 1, 2026

MAJOR Pharmaceuticals is recalling Methylergonovine Maleate Tablets, USP, 0.2 mg due to subpotency — meaning the tablets contain less active ingredient than labeled. The affected lots were distributed nationwide. This is a prescription medication used to control bleeding after childbirth.

Moderate·FDA·Jul 1, 2026

A hardware failure in certain Nissan transmissions can prevent the instrument panel from displaying which gear the vehicle is in. This missing information increases the risk of a crash.

Moderate·NHTSA·Jun 30, 2026

Private Selection Honey Dijon Boneless Skinless Chicken Breasts sold at Kroger and Fred Meyer contain eggs, a known allergen that is not listed on the label. The mislabeling occurred when an incorrect ingredients label was applied to the back of the package. The product is no longer being sold, but some packages may remain in home freezers.

Moderate·USDA·Jun 25, 2026