Check a product

Viatris is recalling one lot of Xanax XR (alprazolam) 3 mg extended-release tablets because they failed to meet dissolution specifications—meaning the tablets may not break down and release the medication properly in your body. This affects only lot #8177156 with an expiration date of 02/28/2027, distributed nationwide. No injuries have been reported.

Moderate·FDA·Apr 15, 2026·Viatris

Preferred Pharmaceuticals' Artificial Tears Lubricant Eye Drops in 0.5 oz bottles may not be sterile due to a manufacturing issue. The FDA is recalling specific lots because sterility cannot be assured. No injuries have been reported.

Moderate·FDA·Apr 15, 2026

Fagron Sterile Services is recalling certain lots of Vancomycin HCl added to 0.9% Sodium Chloride Injection bags (NDC 71266-5085-01). The bags may not be sterile, and a blue break-off part on the administration port could detach. About 16,130 bags were distributed nationwide, and no injuries have been reported.

Moderate·FDA·Apr 15, 2026·Fagron Compounding Services5 products

Fresenius Kabi is recalling 14 sodium chloride and dextrose IV fluid bags because the company cannot assure they are sterile. The products were sold under the Fresenius Kabi, BD and Fresenius Medical Care names and were distributed nationwide, to Alaska and to Puerto Rico. No injuries have been reported.

Moderate·FDA·Apr 15, 202614 products

Cipla is recalling two versions of its lanreotide injection, 120 mg/0.5 mL pre-filled syringes, sold nationwide. The recall was prompted by an FDA observation at the contract manufacturing site about visual inspection procedures, so the product cannot be assured to be sterile. No injuries have been reported.

Moderate·FDA·Apr 15, 20262 products

Morovan gel nail polish remover (15ml bottle, turquoise with white cap) was found to contain methylene chloride and chloroform—chemicals prohibited in cosmetics. Methylene chloride may cause cancer and is not allowed in cosmetics at any level under FDA regulations. About 4,000 units were sold on Amazon between August 2025 and January 2026.

Moderate·FDA·Apr 9, 2026

Quality Meat Sky Ranch marinated beef and pork products sold at Lotte Plaza Market locations contain sesame oil, but sesame was not listed on the label. The affected products were produced between December 1, 2025, and April 6, 2026. No illnesses have been reported, but the products should not be consumed by people with sesame allergies.

Moderate·USDA·Apr 9, 2026

Head USA ski boots from 2015–2022 with fluorescent yellow shells or soles can deteriorate and break during use, creating a serious fall risk. The company has identified specific model numbers and article codes affected by this defect. No injuries have been reported, but the boots pose a hazard if worn.

Moderate·CPSC·Apr 9, 2026

The wires in this decorative light-up buck can be connected incorrectly at the factory, causing a resistor to overheat. This creates a risk of burns or fire. The company has received five reports of smoke and burning smells.

Moderate·CPSC·Apr 9, 2026

Blaine Labs is recalling three lot numbers of Revitaderm and Tridergel wound care gel (1 oz. and 3 oz. bottles/tubes) because they may contain Lysinibacillus fusiformis, a bacterium found in the environment. The affected products were distributed to healthcare providers only, not sold in stores. No injuries have been reported so far.

Moderate·FDA·Apr 8, 2026·Blaine Labs

Cardinal Health Monoject Tuberculin Syringes labeled as 1 mL Luer Lock (Catalog 1180100777) actually contain U-100 Insulin syringes inside the packages. This mislabeling could lead to incorrect dosing if the syringes are used without checking the actual contents. The affected lot numbers are 531164X and 531162X.

Moderate·FDA·Apr 8, 2026

GE Healthcare SIGNA Premier whole-body MRI scanners may have steel fittings instead of brass fittings on the magnet rear. During service work while the magnet is powered up, the magnetic field could pull on these steel parts, risking injury to technicians.

Moderate·FDA·Apr 8, 2026

Oxoid's Microbact 12L Kit (lot 4494873) may produce ambiguous color reactions in test wells that could lead to incorrect organism identification. This affects a limited number of kits distributed in Georgia and California.

Moderate·FDA·Apr 8, 2026·Oxoid

Burlington Medical is recalling 13 radiation protective products, including thyroid shields, vests, kilts, and aprons. The shielding may weaken over time, which shortens how long the garments provide protection. No injuries have been reported.

Moderate·FDA·Apr 8, 2026·Burlington Medical13 products

Civco is recalling 8 eTRAX needle system starter kits and needle sensors used with Aurora trackers. An error in inspection and programming may cause the needle tip position to be shown incorrectly on the user interface. No injuries have been reported.

Moderate·FDA·Apr 8, 2026·Civco8 products

Medline's thoracic robot kits contain Olympus biopsy valves that may shed rubber fragments during use. These fragments could lodge in a patient's airway, potentially requiring removal and causing breathing problems or inflammation.

Moderate·FDA·Apr 8, 20267 products

Summa Therapeutics is recalling certain Finesse BTK Multicath injectable angioplasty balloon catheters because the balloon may not meet burst strength specifications. This could cause the balloon to rupture unexpectedly during a medical procedure. The recall affects 22 units distributed in New Jersey and Florida.

Moderate·FDA·Apr 8, 2026·Summa Therapeutics

Synthes is recalling two bone screw taps, the VOLT Locking Screw Tap and the VOLT Cortex Screw Tap, because two production lots were swapped, so the taps may have an incorrect thread. The recall covers 110 units across 21 states, and no injuries have been reported.

Moderate·FDA·Apr 8, 2026·Synthes2 products

Intuitive Surgical is recalling two da Vinci S and Si reusable surgical instruments, totaling 8,247 units, after the company received complaints of frayed or broken pitch cables. The products were distributed across the U.S. and in many other countries. No injuries have been reported.

Moderate·FDA·Apr 8, 20262 products

Intuitive Surgical is recalling four reusable instrument models used with da Vinci S and Si robotic surgical systems. The company received increased complaints of broken or frayed grip cables. No injuries have been reported, and the instruments were distributed in the U.S. and in many other countries.

Moderate·FDA·Apr 8, 20264 products

Olympus is recalling some SOLTIVE laser systems because a 24V power supply module may fail and make the system inoperable. The defect may also cause smoke or a burning smell, which is designed to stay inside the laser console and extinguish itself. No injuries have been reported. The recall covers 2 products, with 440 units affected, distributed in the US and several other countries.

Moderate·FDA·Apr 8, 20262 products

Medline Industries identified a potential breach in the sterile pouch packaging of one lot of Sterile Radiology Procedure Kits (Model DYNDH1491B). This breach may allow the kit to lose its sterile condition. No injuries have been reported.

Moderate·FDA·Apr 8, 2026

Philips Vue Motion V12 cardiac imaging software (Product Number 1017979, software versions 12.2.0 through 12.2.8.500) may display image frames out of sequence during dynamic cine runs. This could cause medical staff to review cardiac images in the wrong order, potentially affecting diagnosis.

Moderate·FDA·Apr 8, 2026

Medline recalled two products: ENFit G-tube connectors and kits that contain them. The connectors were not made to required dimensions, so they may not seal properly with ENFit-style devices and can leak. No injuries have been reported.

Moderate·FDA·Apr 8, 20262 products

Ultradent Products is recalling Jiffy Original Composite Polisher Cups (Coarse) 12pk because the cups may crumble or break apart during use. This could delay dental treatment. The affected product has lot number 529983 and expiration date of September 2, 2031.

Moderate·FDA·Apr 8, 2026·Ultradent Products

The surgical light assembly in Stryker CHROMOPHARE Softlit Ring systems may not adequately support the weight of the ceiling cover. This could potentially cause the cover to fall. No injuries have been reported.

Moderate·FDA·Apr 8, 2026

Mentor is recalling 7 product lines of breast tissue expanders, including CPX 4 US and Artoura models. The recall notice says the needle tip may be dull or blunt, which could make it hard to advance or cause it to break. No injuries have been reported. The notice refers to infusion sets, while the listed products are tissue expanders, so check the notice for details.

Moderate·FDA·Apr 8, 2026·Mentor7 products

Philips is recalling 22 models of its Allura Xper and Azurion X-ray imaging systems. The recall covers a wired foot switch that may fail to start X-ray imaging or may start it intermittently. No injuries have been reported.

Moderate·FDA·Apr 8, 202622 products

BD Kiestra ReadA lab automation systems (Catalog No. 446948) may occasionally lose remote connectivity after a system reboot, which could temporarily delay plate retrieval from the incubator. The issue is intermittent and does not affect test results, assay performance, or sample integrity. This affects 82 units distributed across the United States and internationally.

Moderate·FDA·Apr 8, 2026·BD Kiestra

Siemens has recalled certain lots of its Atellica CH A1c_E hemoglobin test kit because when used with another reagent (RCRP) on the same analyzer, the A1c test may give lower-than-accurate results. Lower results could delay diabetes diagnosis or lead to inadequate treatment. This issue does not affect labs using separate analyzers for each test.

Moderate·FDA·Apr 8, 2026