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The Adapter for Head Positioning (Model 1739994) used with Baxter operating tables may become loose during patient positioning and move unintentionally. This affects 13 units distributed worldwide, primarily in Minnesota, Maryland, Pennsylvania, Canada, and numerous other countries.

Moderate·FDA·Jul 8, 2026

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, 202612 products

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

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

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

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

Fry Pie Factory pepperoni rolls may contain milk that is not listed on the label. Additionally, some units were not kept refrigerated as required, which can allow harmful bacteria to grow. The recall affects 850 individually packaged 5 oz rolls with sell-by dates from June 12, 2026 through June 21, 2026, distributed in Ohio and West Virginia.

Moderate·FDA·Jul 8, 2026

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, 20262 products

Mars Snacking is recalling two MorningStar Farms vegan products, Buffalo Chik'n Nuggets and Hot & Spicy Sausage Patties, because they may contain pieces of plastic. Both are sold in resealable plastic bags and were distributed in many U.S. states and Puerto Rico. No injuries have been reported.

Moderate·FDA·Jul 8, 2026·MorningStar Farms2 products

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·Lannett

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

Wells Enterprises recalled Blue Ribbon Classics French Vanilla ice cream in 1-gallon containers due to elevated coliform levels detected in the product. The affected ice cream was distributed to one customer in Kenosha, Wisconsin. No illnesses have been reported.

Moderate·FDA·Jul 8, 2026·Blue Ribbon Classics2 products

Certain Harbor Freight Kenway 12V LED Towing Light Kits (model 64282) and 12V Submersible Lights (model 64274) may not illuminate properly. This reduces trailer visibility to other drivers and increases crash risk.

Moderate·NHTSA·Jul 7, 2026·Harbor Freight Tools

Ola-Ola Pounded Yam packages distributed between December 2025 and May 2026 may contain milk (in the form of sodium caseinate) that is not listed on the label. A temporary breakdown in the company's production and packaging processes caused some products to be packaged without proper allergen disclosure. No illnesses have been reported.

Moderate·FDA·Jul 6, 2026

Street's Beef Jerky Teriyaki contains wheat, a known allergen, that is not listed on the product label. The affected products were produced between August 2025 and July 2026 and were sold at three retail locations in Oklahoma. No illnesses have been reported.

Moderate·USDA·Jul 3, 2026

WARN Industries is recalling certain wireless remote kits (part numbers 90287 and 90289) because the handheld remote may not work correctly with some older winches, causing them to move unexpectedly. An unintended winch movement can result in injury.

Moderate·NHTSA·Jul 2, 2026·WARN Industries, Inc.

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

Eunha Fisheries is recalling certain sliced Korean halibut and flounder sashimi products because the included soy sauce and vinegar red pepper paste packets contain wheat, soy, and sesame allergens that are not labeled on the individual condiment packets themselves. People with allergies or sensitivities to these allergens could have a serious or life-threatening reaction.

Moderate·FDA·Jul 1, 2026

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