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Bard Peripheral Vascular is recalling multiple central venous catheter trays and kits because the outer packaging may be damaged, which could compromise the sterile barrier that protects the medical device. The recall affects several Broviac and Hickman catheter products with specific lot numbers manufactured between April 2028 and August 2030.

Moderate·FDA·Feb 25, 2026

Integra LifeSciences is recalling three wound dressing products, including MediHoney Gel, MediHoney Calcium Alginate, and a CVS private label dressing. The packaging may fail, which could break the sterile barrier and let the dressing become contaminated. No injuries have been reported.

Moderate·FDA·Feb 25, 20263 products

Wilson-Cook Medical is recalling certain Teslatome Bipolar Sphincterotomes (medical devices used during endoscopic procedures) because some units may contain a manufacturing defect—a void in the material that separates internal channels. This defect can cause electrical current to flow incorrectly during the cutting procedure.

Moderate·FDA·Feb 25, 2026

Pure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep Reset contain bovine colostrum, which is a milk product, but the label does not warn about the milk allergen. People with milk allergies could have a serious reaction if they use this product.

Moderate·FDA·Feb 25, 2026

Woodland Foods LLC is recalling specific lots of Woodland Gourmet Arrowroot Flour (55 lb. bags) because they may contain foreign material. The affected product was distributed in Kentucky. No injuries have been reported.

Moderate·FDA·Feb 25, 2026·Woodland Gourmet

Indian Kitchen Mart is recalling four cookware products because they may contain lead that can leach into food. The products are sold under the IKM and Indian Kitchen Mart labels, and the kadai also carries the A-Cook name. The recall covers units distributed in California and Colorado, and no injuries have been reported.

Moderate·FDA·Feb 25, 20264 products

Steris Corporation identified that a limited batch of MNA-6x0 adapter components used in the Barco MNA with HexaVue IP Integration System were manufactured with an incorrect configuration file. This affects 10 units with specific serial numbers distributed across seven states.

Moderate·FDA·Feb 18, 2026

The labeling for the Surepulse VS Cap Large, a component of the VS Newborn Heart Rate Monitor, contains an incorrect sizing guide. This labeling error could lead to improper fit of the cap during use. No injuries have been reported.

Moderate·FDA·Feb 18, 2026·SurePulse Medical5 products

Philips is recalling eight Azurion 3, 5, and 7 X-ray system models. Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed, even when a table lock is active. No injuries have been reported.

Moderate·FDA·Feb 18, 20268 products

Alphatec Spine has recalled its ATEC Lateral Navigation Disc Prep Osteotome (10mm, model 266-01-000-10-N) used in spinal surgery due to an incorrect connection geometry in the navigated array. This defect could affect how the instrument connects to the Medtronic StealthStation navigation system during surgery. Seven units were distributed across 14 U.S. states.

Moderate·FDA·Feb 18, 2026·Alphatec Spine2 products

Certain Laerdal Compact Suction Unit 4 RTCA models made during a specific time period may emit electromagnetic noise above acceptable levels for aircraft use. No injuries have been reported. The affected units have specific catalog numbers: 880052, 880062, or 881152.

Moderate·FDA·Feb 18, 2026·Laerdal

Halyard TRANSPORT BAG KIT (Kit Code LIFE0080-01) may have a defective Tyvek bag seal that could compromise the sterility of the kit. The issue affects approximately 1,500 units distributed in New Jersey. No injuries have been reported.

Moderate·FDA·Feb 18, 2026

Straumann USA LLC recalled certain WB Impression Post Closed Tray kits because they contain magenta impression caps instead of the correct brown caps. This mix-up could lead to using the wrong component during dental implant procedures. The recall affects 561 units distributed nationwide.

Moderate·FDA·Feb 18, 2026

Medline is recalling 11 kit products that contain BD ChloraPrep Triple Swabsticks. BD found that the applicator packaging may have an open seal. No injuries have been reported.

Moderate·FDA·Feb 18, 202611 products

Philips is recalling four CT scanner models because one or more of the 32 fasteners that attach the rotor to the gantry bearing may not be tightened to specification. If several fasteners are loose, rotor parts could become unsecured or displaced, and in theory could be expelled. The company reports no injuries and no observed parts being expelled during gantry rotation.

Moderate·FDA·Feb 18, 20264 products

Hologic's Brevera Breast Biopsy System disposable 9 gauge needles may contain tiny particles that could be deposited into breast tissue during a biopsy procedure. This affects approximately 681,870 units distributed nationwide. No injuries have been reported so far.

Moderate·FDA·Feb 18, 2026

TKS Co-pack Manufacturing is recalling 2 products: Aonic Complete Hers and Aonic Complete His, single-serving 34 ml liquid dietary supplement shots in plastic bottles. The recall was issued because the products may contain coliforms, E. coli, or Pseudomonas aeruginosa. The products were distributed to a customer in Utah, and no injuries have been reported.

Moderate·FDA·Feb 18, 20262 products

Karison Foods & Snacks is recalling five 12-ounce Karison sweets: Besan Laddoo, No Sugar Added Besan Laddoo, Punjabi Pinni, Alsi Pinni and Panjiri. The products contain milk, which is not listed on the ingredient label. The sweets were distributed in New York, New Jersey and Virginia, and no injuries have been reported.

Moderate·FDA·Feb 18, 20265 products

Ventura Foods LLC recalled multiple brands of peanut butter after finding pieces of blue plastic in a production filter. The affected products were distributed under several brand names including US Foods, Dyma Brands, Flavor Fresh, House Recipe, Katy's Kitchen, Gordon Food Service, and Poco Pac, shipped to 39 states. No injuries have been reported.

Moderate·FDA·Feb 18, 2026·Ventura Foods3 products

Cacao Art Crunchy Caramel artisan dark chocolate bars contain milk from butter and cream ingredients, but milk is not listed on the package label. This poses a serious risk to anyone with a milk allergy. The product was distributed only in Florida.

Moderate·FDA·Feb 18, 2026

Domino Foods' Sodexo Stars Saccharin (pink) packets contain aspartame that was not listed on the label. People with phenylketonuria (PKU) or those avoiding aspartame need to know what's in their sweetener. The affected packets were distributed across 14 states.

Moderate·FDA·Feb 18, 2026

Red Button Movie House Popcorn (24 oz bags) may contain foreign material such as glass, plastic, or metal fragments. The affected product was distributed to stores in Utah, Arizona, Idaho, Colorado, Montana, Oregon, Nevada, and Wyoming. No injuries have been reported so far.

Moderate·FDA·Feb 18, 2026·Red Button Movie House

MG Foods Spicy Breakfast Burritos may contain small hard plastic fragments. The recall affects 3,099 units with Fresh Thru dates between January 21 and January 27, 2026, distributed across the Midwest. No injuries have been reported.

Moderate·FDA·Feb 18, 2026·MG Foods

Island Crab Corporation's smoked grouper dip contains milk, eggs, and sodium metabisulfite that are not listed on the label. This product was distributed in Florida in 7-pound plastic tubs with expiration dates between January 20 and January 26, 2026. People with allergies or sensitivities to these ingredients could have a serious reaction if they consume this product without knowing these ingredients are present.

Moderate·FDA·Feb 18, 2026

McCain is recalling two frozen potato products, Ore-Ida Tater Tots shaped potatoes (item OIF00215A) and Sonic Tots (item SON00543), because they may contain small hard plastic fragments. They were sold in 30-pound cases of six 5-pound clear, unlabeled bags, and the recall covers 21,557 cases of Ore-Ida and 67 cases of Sonic, distributed in 28 states. No injuries have been reported.

Moderate·FDA·Feb 18, 2026·Ore-Ida2 products

Preema brand Bright Red and Orange Food Colour Powders contain carmoisine, a banned food dye, and undeclared FD&C Yellow 5 and FD&C Red 40. These undeclared dyes may cause allergic reactions in sensitive individuals and can affect attention in children. The products were distributed in New York and Massachusetts.

Moderate·FDA·Feb 18, 2026

Meitheal Pharmaceuticals is recalling Cetrorelix Acetate 0.25 mg injection kits because some contain missing or duplicated needles in the delivery system. This affects lot Q4E0112A with an expiration date of April 30, 2027. The defect could prevent proper injection or cause unsafe handling.

Moderate·FDA·Feb 18, 2026·Meitheal Pharmaceuticals

American Health Packaging is recalling certain oxycodone hydrochloride 5 mg tablets because the blister card seals are defective or missing. This allows tablets to fall out of their compartments. The recall affects 31,676 packages distributed nationwide with specific lot numbers and expiration dates.

Moderate·FDA·Feb 18, 2026

Fresenius Kabi Compounding has recalled five specific lots of ketamine HCl injection (10 mg per mL) distributed nationwide because the manufacturer cannot confirm the product remains sterile. The affected lots were produced between February and April 2026.

Moderate·FDA·Feb 18, 20265 products

Asteria Health is recalling estradiol hormone pellets (10 mg) because they may contain metal particles. The affected pellets were distributed nationwide. No injuries have been reported so far.

Moderate·FDA·Feb 18, 2026·Asteria Health25 products