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Edermy is recalling two PIE medical device products that did not have the required FDA 510(k) clearance. The recall covers 27 PIE Trolley System units and 11,202 PIE PAK units, sold nationwide in 18 states. No injuries have been reported.

Moderate·FDA·Mar 4, 2026·Edermy2 products

Encore Medical is recalling 3 implant products, 54 units in total, because the labeling on the knee and humeral socket implants is incorrect. The implants were distributed across the US in 17 states. No injuries have been reported.

Moderate·FDA·Mar 4, 2026·Encore Medical3 products

Olympus is recalling 20 urological and gynecological resection sheath and inner sheath models sold across the US. The company received complaints that the ceramic tip of the resection sheath can break. No injuries have been reported, and the agency has not specified a remedy.

Moderate·FDA·Mar 4, 202620 products

Olympus is recalling the Cystoscope Outer Sheath model WA22810A because it is incompatible with GreenLight Laser systems used for prostate (BPH) treatment. Using this sheath with the laser can damage the tip of the device, potentially affecting the safety and function of the cystoscope.

Moderate·FDA·Mar 4, 2026

MRIMed's SL-111 battery for the Mobile Exam Light (model SL-110) can overheat while charging, causing internal components to melt and create smoke. This affects 314 batteries with specific lot numbers distributed nationwide and internationally.

Moderate·FDA·Mar 4, 2026

Medline reported that the manufacturer of its sterile saline wound wash may not have made the products to the required sterility assurance level. The recall covers five products: a saline wound wash sold under the Medline and Meijer names, plus several Medline convenience kits. No injuries have been reported, and the products were distributed across the US and to the Bahamas, Bermuda, and the Cayman Islands.

Moderate·FDA·Mar 4, 20265 products

Hitachi is recalling two proton beam therapy systems because a software problem in the patient positioning system may cause the patient's position to be slightly off target. The recall covers two products, with one unit affected in each, distributed to Texas and Washington, D.C. No injuries have been reported.

Moderate·FDA·Mar 4, 2026·Hitachi2 products

Wellsley Farms Farm-Raised Atlantic Salmon (32 oz packages) has been recalled because it may be contaminated with Listeria monocytogenes, a bacteria that can cause serious illness. The affected product was produced on June 30, 2025, with a best-by date of June 30, 2027.

Moderate·FDA·Mar 4, 2026

Valley Springs/Artesian Gold recalled three 1-gallon water products sold as Valley Springs 100% Natural Bottled Water (including a fluoride-added version) and Valley Springs Steamed Distilled Water. The water was bottled under insanitary conditions. The products were distributed in Illinois and Wisconsin, and no injuries have been reported.

Moderate·FDA·Mar 4, 2026·Valley Springs3 products

SB Food is recalling three Yoyo gummy candy products: Assorted Flavor, Tropical Flavor, and Grape Plus Flavor, each in 2.8 oz (80g) plastic bags. The gummies contain Carmoisine (E122, also called Acid Red 14), a color not permitted in this product. The products were sold in AR, GA, IA, IN, KY, MD, MN, NE, NY, OH, PA, TN, TX, VA and WA. No injuries have been reported.

Moderate·FDA·Mar 4, 20263 products

YO!MAN Lettuce (Spicy Flavor) contains cyclamates, an artificial sweetener not declared on the label. Cyclamates are banned in the United States and were not listed in the ingredient information. The affected product was distributed in limited quantities to New York, Pennsylvania, Florida, Louisiana, and Texas.

Moderate·FDA·Mar 4, 20262 products

Lubna Quality Products mung beans sold in 4lb bags were found to contain Thiamethoxam, a pesticide. The affected product was distributed to Texas and Louisiana in January 2025. No illnesses have been reported.

Moderate·FDA·Mar 4, 2026

Tiki Bar Candy Dark Chocolatey Peanut Butter & Pretzel bars contain peanuts listed in the ingredients, but the allergen warning label fails to clearly declare peanut as an allergen. This mislabeling poses a serious risk to people with peanut allergies. The recall affects only products distributed in Hawaii with a best-by date of 11/26 or earlier.

Moderate·FDA·Mar 4, 2026

Wizcure Pharma is recalling seven eye products sold nationwide: Vista dry eye drops (Vista Tears, Vista Gel, Vista Meibo Tears and Vista Gonio), Bio Glo and BioGlo fluorescein diagnostic test strips, and CHNaO fluorescein test strips. The FDA says the products were not made under current good manufacturing practices, so the company cannot assure they are sterile. No injuries have been reported.

Moderate·FDA·Mar 4, 2026·Wizcure Pharma7 products

The FDA says Agebox iKids-Growth capsules contain ibutamoren, an ingredient that is not listed on the label and is not approved for use in these products. The recall covers two products, both sold as 60-count bottles of Agebox iKids-Growth capsules: a Day Formula and a Night Formula. No injuries have been reported.

Moderate·FDA·Mar 4, 20262 products

Slate Run Pharmaceuticals is recalling Eptifibatide Injection 75 mg/100 mL vials because the carton label says "weight-adjusted bolus dosing" when it should say "weight-adjusted infusion." This labeling error could lead to incorrect administration of the medication. No injuries have been reported.

Moderate·FDA·Mar 4, 2026·Slate Run Pharmaceuticals

AvKARE is recalling one lot of Amantadine HCl 100 mg capsules because they failed to meet dissolution specifications—meaning the capsules may not break down properly in the body, affecting how much medicine you receive. This is a quality issue identified during manufacturing testing. No injuries have been reported.

Moderate·FDA·Mar 4, 2026·AvKARE

LEO Pharma is recalling specific lots of Adbry, a prescription injection used to treat atopic dermatitis, because one unit was found to contain wool fiber particles. This contamination raises concerns about sterility and safety. No injuries have been reported so far.

Moderate·FDA·Mar 4, 2026·Leo Pharma

Several beef jerky products sold in Hawaii and online contain soy lecithin that is not listed on the label. Soy is a common allergen that can cause serious reactions in people with soy allergies. The products are no longer being sold, but some may still be in home pantries.

Moderate·USDA·Mar 1, 2026

Andersen Windows is recalling opening control devices on 100 Series casement windows manufactured before November 19, 2025. These devices can break or detach after impact, allowing windows to open unexpectedly and creating a fall risk, especially for children. No injuries have been reported, but eight instances of device failure have been documented.

Moderate·CPSC·Feb 26, 2026

Moisture can get trapped inside these bath foam containers and build up pressure. When opened, pieces may shoot out forcefully and hit someone. The company has received three reports of injuries, including bruises, swelling, and a chipped tooth.

Moderate·CPSC·Feb 26, 2026·Surreal

A software update (version P1.2.1) for the Intuitive Surgical Da Vinci 5 surgical system can cause the user interface to disappear from external or tower monitors during use. This affects 12 systems distributed in six U.S. states. No injuries have been reported.

Moderate·FDA·Feb 25, 2026

Stryker is recalling certain MOLLI 2 surgical marker systems because the instructions for use need to be updated. Magnetized surgical tools used during the procedure may dislodge the markers that are placed to mark the surgical site. Stryker is providing updated labeling to address this issue.

Moderate·FDA·Feb 25, 2026

Centinel Spine's Prodisc C SK cervical disc replacement devices were labeled as 6mm but actually contained 5mm products. This mislabeling affects 20 units distributed across eight states. The size difference could affect surgical fit and patient outcomes.

Moderate·FDA·Feb 25, 2026·Centinel Spine

Medline is recalling 42 convenience kits and procedure packs that were sterilized and packaged on equipment with calibration problems. The kits went through the validated sterilization and packaging cycles, but the calibration issues could affect how reliably they are sterile. No injuries have been reported.

Moderate·FDA·Feb 25, 202642 products

The MONARCH Platform bronchoscopy device has a software issue that can cause the robotic arm to move unexpectedly. If the application restarts after you select a position but before loading the bronchoscope, the system may reset to the left side even if you selected right, potentially causing the arm to contact the patient or breathing tube.

Moderate·FDA·Feb 25, 2026·Auris Health

Olympus is removing 12 versions of its Thunderbeat surgical energy device from the market because it has continued to receive reports of adverse events. About 107,000 units are affected, and the devices were sold in the US and in Brazil, Canada, Germany, Mexico, and Japan. The recall notice does not list any reported injuries.

Moderate·FDA·Feb 25, 202612 products

Medica Corporation's capillary tubes used with EasyBloodGas and EasyStat devices are giving false potassium results—up to 20% higher than actual levels. This could lead doctors to misinterpret a patient's potassium levels and provide incorrect treatment.

Moderate·FDA·Feb 25, 2026·Medica

Immunotech's Estrone RIA diagnostic kit may rarely produce falsely high hormone test results in patients. This could potentially lead to unnecessary or incorrect medical decisions. The issue affects only specific lot numbers and occurs very infrequently.

Moderate·FDA·Feb 25, 2026·Immunotech

Baxter Healthcare released 5 Spectrum IQ infusion pumps (model 3570009) without completing required safety tests, including tests of the occlusion alarm that alerts users to blockages. The pumps were distributed in Ohio. No injuries have been reported.

Moderate·FDA·Feb 25, 2026