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Booey's Gourmet Dragon's Breath sauce contains anchovy (fish) and sesame, but the label's "Contains" statement does not list these allergens. The ingredients list does mention them, but people with fish or sesame allergies may not see the warning they need. About 870 bottles were sold in Washington state.

Moderate·FDA·Apr 22, 2026

Avantor Performance Materials has recalled Magnesium Chloride, 6-Hydrate Crystal (500G bottles, Lot 23G3161005, expiration 9/21/2027) because the product does not meet strength specifications. This bulk pharmaceutical ingredient may be less potent than labeled.

Moderate·FDA·Apr 22, 2026·Avantor

Island Kinetics, Inc. (d.b.a. CoValence Laboratories) is recalling specific lots of Skin Script Blemish Spot Treatment because the product failed stability testing. This means the product may not maintain its intended strength or safety over time. No injuries have been reported.

Moderate·FDA·Apr 22, 2026·CoValence Laboratories

Major Pharmaceuticals is recalling memantine hydrochloride extended-release 7 mg capsules (lot N02425, expiring 05/31/2027) because the capsules may not dissolve properly in the body. This means the medication may not work as intended. The affected capsules were distributed nationwide.

Moderate·FDA·Apr 22, 2026

International Medication Systems Ltd. is recalling one lot of epinephrine injection due to concerns that the sterility of the product cannot be assured. The affected lot (EA038A5, expiring 08/2026) was distributed nationwide. No injuries have been reported.

Moderate·FDA·Apr 22, 2026·International Medication Systems

CoValence Laboratories is recalling three hydrocortisone 1% skin gels because they may contain less hydrocortisone than the label states. The recall covers Remedy Gel (distributed by glo Skin Beauty), and Skin Rehab Calming Skin Gel and Essential Calming Skin Gel (both distributed by A.C.E. Inc.). No injuries have been reported.

Moderate·FDA·Apr 22, 2026·CoValence Laboratories3 products

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

Q'Straint QRT-3 wheelchair retractors may fail to lock properly, leaving wheelchairs unsecured during vehicle transit. An unsecured wheelchair can shift or move, potentially causing injury to the user or others.

Moderate·NHTSA·Apr 20, 2026·Q'Straint

Certain Goodyear Eagle F1 Supersport tires (sizes 305/30ZR21 and 255/35ZR20) may experience tread separation. This can cause loss of control and increase crash risk. Goodyear has notified owners and arranged for free replacement or refund.

Moderate·NHTSA·Apr 18, 2026·Goodyear Tire & Rubber Company

Fun and Function's metal multi-point swing frames (model MW7661) can crack or break during use, causing children to fall. The company has received 10 reports of frames cracking or breaking, with two children sustaining bruises.

Moderate·CPSC·Apr 16, 2026

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

Tornier, Inc. recalled three shoulder implant parts that were incorrectly labeled as compatible with the Tornier HRS Max system. These parts actually work only with the older Tornier HRS system and will not fit properly in HRS Max procedures. A total of 233 units with specific lot numbers were distributed nationwide.

Moderate·FDA·Apr 15, 2026·Tornier

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

Riverence Provisions LLC is recalling Smoked Trout Dip because the label does not declare milk, even though the product contains cream cheese and sour cream. People with milk allergies could have a serious reaction if they eat this product. The recall affects specific lot numbers distributed across several states.

Moderate·FDA·Apr 15, 2026

F&S Fresh Foods ReadyMeals Turkey Bacon & Cheddar Pretzel Duo Sandwich contains sesame that is not listed on the label. The sandwich has visible sesame seeds, but the package only declares egg, milk, soy, and wheat as allergens. This poses a serious risk to people with sesame allergies.

Moderate·FDA·Apr 15, 2026

Mei Yu Cheng Da is recalling two products: Dadi Nongfu dried salt chilli vegetables and Olive Skewers in 500g clear bags. The products contain cyclamates, a sweetener banned in U.S. foods. They were distributed in New York, Pennsylvania and Florida, and no injuries have been reported.

Moderate·FDA·Apr 15, 20262 products

Zarlengo Italian Ice is recalling three Zarlengo's gelato products: Chocolate Chocolate Chip Gelato, Chocolate Gelato, and Double Dark Chocolate Gelato. They come in sizes from 6 fl oz cups to 2-gallon buckets and were distributed in Illinois, Indiana, and Texas. The ingredients list includes soy lecithin, but soy is not listed in the allergen statement, so the products could be unsafe for people with a soy allergy.

Moderate·FDA·Apr 15, 20263 products

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