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Nephron SC is recalling albuterol sulfate inhalation solution (0.5%, 30x5 mL vials, Lot AB6001, expiring 1/15/2027) because the labels are illegible and cannot be read clearly. This makes it difficult to verify the correct dose and medication details. The recall affects 146,280 vials distributed nationwide.

Moderate·FDA·Apr 22, 2026·Nephron

Taro Pharmaceuticals is recalling one lot of fluocinonide 0.05% cream due to a manufacturing defect. Testing found the cream's thickness was thicker than specifications allow, which could affect how the medication works on your skin.

Moderate·FDA·Apr 22, 20263 products

Payless Compounders is recalling a compounded semaglutide injection due to lack of assurance of sterility. The affected product is a 0.5 mL vial from lot 01-27-2026@14S.5 distributed in Oregon. No injuries have been reported so far.

Moderate·FDA·Apr 22, 2026·Payless Compounders

Kang Zhongyuan is recalling 15 menthol cough drop products after an FDA inspection of the manufacturing facility on August 15, 2025 turned up observations that may affect product quality. The products are sold under the names exchange select, caring mill, Discount Drug Mart Food Market, MGC Health and QC Quality Choice, and are distributed nationwide. No injuries have been reported.

Moderate·FDA·Apr 22, 2026·Kang Zhongyuan15 products

Owen Biosciences is recalling four benzoyl peroxide acne products over possible benzene contamination, a chemical linked to cancer with long-term exposure. The products are FHF Farmhouse Fresh Midnight Clearing Night Lotion, HydroPeptide Clear Alliance Serum, and two SLMD (Sandra Lee MD) acne products, distributed by Skin PS Brands. No injuries have been reported.

Moderate·FDA·Apr 22, 2026·Owen Biosciences4 products

Cipla USA is recalling specific lots of Cinacalcet Hydrochloride 30 mg tablets because they contain higher-than-acceptable levels of a chemical impurity called N-Nitroso Cinacalcet. The affected tablets were distributed nationwide. This is a manufacturing quality issue; no injuries have been reported.

Moderate·FDA·Apr 22, 20263 products

Brahms GmbH is recalling certain lots of the B.R.A.H.M.S PlGF Plus KRYPTOR, a blood test used to assess preeclampsia risk during pregnancy. Quality control checks at the lowest level (QC Level 1) may show out-of-range values that could mask an underlying problem if not performed correctly. This could lead to falsely high test results that overestimate preeclampsia risk.

Moderate·FDA·Apr 15, 2026·Brahms

Certain Spacelabs Healthcare Model 91496 multi-parameter cardiac monitors have a circuit board defect. When the device is in Auto mode, the cardiac output measurement may start too early, causing errors that prevent proper readings or exclude readings that should be included. This could lead to inaccurate patient information and delayed medical decisions.

Moderate·FDA·Apr 15, 2026·Spacelabs Healthcare

Cook Medical is recalling 18 product listings, including catheter, tracheostomy, and central venous kits and trays, because some affected lots were labeled with expiration dates longer than their true shelf life. No injuries have been reported, and the products were distributed worldwide.

Moderate·FDA·Apr 15, 202618 products

Molded Products Inc. is recalling the MPC-130 See Luer Cap Set used in medical IV administration. The threaded sleeve can fail to engage properly, causing the cap to become detached during use. This affects 26,900 units distributed across Tennessee, Texas, Nevada, Illinois, and Florida.

Moderate·FDA·Apr 15, 2026·Molded Products

Two units of XTANT Medical Xpress Pedicle Screw System (Part Number X073-6555-DL, Lot 4375-01) were mislabeled with an incorrect part number. The label indicates a shorter screw length than what the device actually is, which could cause confusion during surgical use.

Moderate·FDA·Apr 15, 2026·Xtant Medical

Beckman Coulter identified a manufacturing defect in certain MicroScan Neg MIC 3J antibiotic susceptibility test panels (Catalog C54814, Lot 2025-08-23). Some panels are missing a drug in one well and contain double the amount of antibiotics in others, which could produce inaccurate test results. No injuries have been reported.

Moderate·FDA·Apr 15, 2026

Siemens ARTIS pheno and ARTIS Icono biplane imaging systems may occasionally display an incorrect, higher x-ray dose reading during patient exams. The actual radiation dose delivered is safe and meets regulatory standards, but the displayed reading can be misleading. This affects certain model numbers used in hospitals and imaging centers.

Moderate·FDA·Apr 15, 2026

Teva Pharmaceuticals is recalling certain Clonidine Transdermal System patches (0.1 mg/day) because they were manufactured using an unapproved raw material that does not meet FDA standards. The affected patches were distributed in the U.S. The company and FDA are working to ensure the product is removed from use.

Moderate·FDA·Apr 15, 20263 products

GE Healthcare has recalled specific lots of Omnipaque (iohexol) injection, a contrast dye used in medical imaging, because some vials may contain visible particles. This could affect the safety of the procedure if the contaminated solution is used.

Moderate·FDA·Apr 15, 20262 products

Teva is recalling two strengths of isotretinoin capsules, 30 mg and 40 mg, because some capsules may be stronger or weaker than the labeled amount. The recall covers 10-count prescription packs distributed in Florida, Ohio, Puerto Rico and Mississippi, and no injuries have been reported.

Moderate·FDA·Apr 15, 20262 products

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

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