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Unichem Pharmaceuticals distributed 60,000 tablets of Doxazosin 4 mg with incorrect imprinting on the tablets themselves. This labeling error could cause confusion about the medication's identity and strength. The affected lot is GDSH25006, which expires in August 2027.

Moderate·FDA·Feb 18, 2026·Unichem Pharmaceuticals

Pro Numb is recalling two tattoo numbing sprays because they were made in ways that did not meet FDA manufacturing standards. The recall covers Pro Numb Tattoo Numbing Spray 5% Lidocaine and Pro Numb Tattoo Numbing Spray For Sensitive Skin 4% Lidocaine, sold nationwide in the USA. No injuries have been reported.

Moderate·FDA·Feb 18, 2026·Pro Numb2 products

Etac is recalling four Molift mobile patient hoist and sling bar products, covering 255 affected units. A customer reported that the bolt mounting the lifting bar broke during assembly and load testing. The company found that material deformation between the lifting bar and the device arm can limit joint mobility and stop the equipment from working properly. No injuries have been reported.

Moderate·FDA·Feb 11, 2026·Etac4 products

Fujirebio is recalling seven Lumipulse plasma test products used to measure amyloid and pTau217 for Alzheimer's disease. The tests can produce falsely elevated results, which may wrongly classify a patient as having Alzheimer's-related amyloid pathology or lead to unneeded additional testing. No injuries have been reported.

Moderate·FDA·Feb 11, 2026·Fujirebio7 products

Maquet Cardiopulmonary identified a durability problem with the connecting cable on its Venous Bubble Sensor (Model 701055720). Excessive bending of the cable can damage the sensor or loosen the connection, causing error messages on the connected medical device—either temporarily when the cable moves or permanently if the connection fails.

Moderate·FDA·Feb 11, 2026

FUJIFILM Healthcare Americas has recalled certain FDR Visionary Suite X-ray systems (Model CH-200) because internal electrical contacts can become welded together. This may allow power to continue flowing to the system even after it is turned off, which could cause the circuit to overheat, damage nearby parts, and create smoke.

Moderate·FDA·Feb 11, 2026

Wilson-Cook Medical is recalling certain nasal jejunal feeding tubes (model NJFT-10) because some units were shipped without the nasal transfer tube component, making them incomplete and unusable. The recall affects 60 units distributed in Australia.

Moderate·FDA·Feb 11, 2026

Olympus is recalling 30 sphincterotome devices, which are used with an endoscope during medical procedures. Some units were not thermoformed as required and could deform, losing performance. No injuries have been reported.

Moderate·FDA·Feb 11, 202630 products

Changchun Wancheng is recalling 11 product listings of home test strips and diagnostic tests, including urinary tract infection, ovulation, menopause, fertility and Vivoo tests. The devices were distributed in the U.S. before FDA clearance (510(k)), and they may give false or inaccurate results to users, which could lead to inappropriate medical treatment. The recall was distributed nationwide, with confirmed distribution in Texas, Georgia and California.

Moderate·FDA·Feb 11, 2026·Changchun Wancheng11 products

Vortex Surgical is recalling 13 ophthalmic surgical products, including laser probes, forceps, cannulas, and related kits, because the Tyvek pouch seals may have voids. A damaged seal can compromise the sterile barrier and allow bioburden contamination, which could lead to infection. No injuries have been reported.

Moderate·FDA·Feb 11, 2026·Vortex Surgical13 products

Focalyx Fusion, a software device used to guide prostate biopsies and diagnostic procedures, may not work properly on Windows 10 operating systems. This malfunction could harm patients during biopsy or delay needed treatment. The manufacturer recommends stopping use of affected software versions until the device is confirmed to work with Windows 11.

Moderate·FDA·Feb 11, 2026·Focalyx

Siemens is recalling three brain imaging software applications installed on certain CT systems because they have not received FDA 510(k) clearance. The recall covers 4 CT system models, with 97 units affected, distributed in the US and Canada, Costa Rica, India, and Israel. No injuries have been reported.

Moderate·FDA·Feb 11, 20264 products

A specific lot of Tornier surgical screws (catalog DWJ318, lot AZ4824290) is labeled as 5.0mm×18mm but actually contains 5.0mm×14mm screws. If the wrong size is used without detection during surgery, it could increase the risk of mechanical failure and the need for revision surgery.

Moderate·FDA·Feb 11, 2026·Tornier

Biomerieux VITEK 2 Gram-negative Susceptibility Cards used to test bacterial resistance to certain antibiotics may produce incorrect results or fail quality control checks. The affected cards test bacteria such as E. coli and Pseudomonas aeruginosa against five antibiotic types. Inaccurate results could lead to inappropriate treatment decisions.

Moderate·FDA·Feb 11, 2026

A software error in the Beckman Coulter CellMek SPS Sample Preparation System (model C44603, software version 2.3.90.0) causes samples to be dispensed incorrectly, potentially damaging the instrument and losing 60–100 microliters of sample fluid. This could lead to inaccurate test results and incorrect patient care decisions.

Moderate·FDA·Feb 11, 2026

Encore Medical is recalling two EMPOWR surgical device products, 68 units in total, because some packages may contain the wrong acetabular system or may have a packaging discrepancy. One acetabular system package was found to contain a different device, and other acetabular system and knee insert devices may be affected. The problem could delay surgery while devices are exchanged or lead to a revision surgery. No injuries have been reported.

Moderate·FDA·Feb 11, 2026·Encore Medical2 products

A software error allowed robotic instrument arms with bent or misaligned parts to remain in use during surgery. These parts can wear out and potentially fail during a procedure. Intuitive Surgical identified specific serial numbers of affected systems.

Moderate·FDA·Feb 11, 2026

Vantive is recalling eight Prismaflex and Oxiris dialysis set products distributed nationwide. The deaeration chamber on these sets may become dislodged from the Prismaflex Control Unit. No injuries have been reported.

Moderate·FDA·Feb 11, 2026·Vantive8 products

Olympus Corporation is recalling certain single-use electrosurgical knives (model KD-640L) used during endoscopic surgery. The cutting knife can overheat, burn, and break during use, which could affect the surgery. No injuries have been reported.

Moderate·FDA·Feb 11, 20262 products

Beckman Coulter has recalled specific lots of COULTER DxH Diluent and COULTER DxH ECO Diluent used in blood cell analysis systems. These affected lots can produce inaccurate platelet count readings during daily quality checks, which may lead to unreliable test results.

Moderate·FDA·Feb 11, 2026

Willy Pete's Chocolates Almond Despair dark chocolate contains almonds, but almonds are not listed in the ingredient statement. The product name and front label mention almonds, but people with tree nut allergies relying on the ingredients list may not know almonds are present.

Moderate·FDA·Feb 11, 2026

Imu-Tek Immuno-5 Colostrum Powder (7 oz) contains milk that is not listed on the label. This poses a serious risk to people and pets with milk allergies or sensitivity. The affected product is Lot #216 with an expiration date of 4/16/2027.

Moderate·FDA·Feb 11, 2026

Venzu Traders LLC cinnamon powder (3.5 oz/100g packages) may contain high levels of lead. The product was distributed in California, Nevada, and Washington. No illnesses have been reported, but lead exposure can cause serious health problems, especially in children.

Moderate·FDA·Feb 11, 2026

Spicely is recalling three organic spice products sold in jars: garlic salt, celery salt, and sumac. The labels say "NO SALT," but the products contain salt. No illnesses or injuries have been reported. The jars were sold in CA, CO, IL, IN, MI, NC, NY, OH, OR, PA, TX, UT, and WA.

Moderate·FDA·Feb 11, 2026·spicely3 products

Beacon Promotions is recalling two repackaged M&M's candy products because they contain milk, soy and peanut without those allergens being listed on the label. One is Make Your Mark peanut M&M's, and the other is M&M's candies labeled with promotional company names such as Next Up, Smith Pro, Jaxport, Climax Molybdenum and more. The candies were sent to 20 states, and no injuries have been reported.

Moderate·FDA·Feb 11, 20262 products

WinCo Foods is recalling Deli Margherita Pizza Thin Crust (17 oz, Item #67279) because some packages may contain metal fragments. The pizza is sold refrigerated as a take-and-bake product and was distributed to stores in the western and south-central United States.

Moderate·FDA·Feb 11, 2026

Prima Foods is recalling six BarbaCuban sauces, marinades and ketchup sold in 12 oz glass bottles and larger jugs, including 455 Everything Sauce (Original and Hot), 90 Miles to Mojo Marinade, Ram Air Red Zesty Ketchup, Cubama White Truffle Sauce and Havana Gold. The products may contain quinine, which is not listed on the label. The recall covers products distributed in Florida.

Moderate·FDA·Feb 11, 20266 products

Fazt & Loud LLC is recalling Lost and Found Energy Sour Gummy Bear drinks because the label says each can has 150mg of caffeine, but they actually contain 300mg—twice as much. This mislabeling affects 16oz cans from lot MO-00911 with a best-by date of 11/13/2027 distributed nationwide.

Moderate·FDA·Feb 11, 2026·Lost and Found Energy

Rich Products' Gluten Free 14" Seasoned Vegan Pizza Crust contains milk and egg that are not listed on the label. The product is labeled "vegan" and says it "may contain" milk and eggs, but the milk and egg are actually present in the product itself. This poses a serious risk to people with milk or egg allergies.

Moderate·FDA·Feb 11, 2026

Sun Pharmaceutical is recalling one lot of Diclofenac Sodium Topical Gel, 3% (Lot #AD92721, expiring 3/31/2027) because the gel's thickness is slightly lower than required specifications. The product was distributed nationwide and is sold by prescription only.

Moderate·FDA·Feb 11, 2026