Alaska recalls

Sold nationwide. LeMaitre Vascular is recalling one unit of Artegraft Vascular Graft (Model AG740) distributed in Illinois due to a labeling mix-up on the outer packaging. The product box was labeled with an incorrect lot number, which could cause confusion during clinical use. No injuries have been reported.

Moderate·FDA·Mar 25, 2026·LeMaitre Vascular

Sold nationwide. The Welch Allyn Spot Vision Screener VS100 (software version 3.2.0.1) may display an unintended flickering screen due to a software issue. Flickering lights can trigger seizures in people who are photosensitive.

Moderate·FDA·Mar 25, 2026·Baxter

Sold nationwide. The external screws that secure the cover on the Howmedica Osteonics MICS3 Angled Sagittal Saw Attachment may loosen during use and detach. This affects all units with part number 210490 distributed across the United States and several other countries. No injuries have been reported.

Moderate·FDA·Mar 25, 2026·Howmedica Osteonics

Sold nationwide. GE is recalling three versions of Centricity Universal Viewer software, a program that displays medical images, including mammograms. User login credentials may be exposed on the local workstation, which could let an unauthorized person affect system availability or manipulate data. The recall covers 2,405 affected units, and no injuries have been reported.

Moderate·FDA·Mar 25, 2026·GE3 products

Sold nationwide. Abbott Diagnostics has recalled certain lots of the ID NOW Influenza A & B 2 test kit because they produce an unusually high number of invalid results compared to what the instructions say to expect. Invalid results mean the test does not give a clear positive or negative answer, requiring a retest.

Moderate·FDA·Mar 25, 2026·Abbott

Sold nationwide. Blackwing Organic Meats sold beef and pork products that were produced without required federal inspection and some bear false USDA inspection marks. These products may contain harmful bacteria, allergens, or other contaminants. The affected products were produced between April 2024 and March 2026 and shipped nationwide.

Serious·USDA·Mar 25, 2026·Blackwing Organic Meats

Sold nationwide. MID EAST Jordanian Zaatar spice mix in 5 lb bags contains sesame and wheat that are not listed on the label. This product was distributed to bakeries for use in breads and pastries. People with sesame or wheat allergies could have a serious reaction if they consume products made with this spice mix.

Serious·FDA·Mar 25, 2026·MID EAST

Sold nationwide. Apotex Corp. is recalling specific lots of brimonidine tartrate/timolol maleate eye drops because the manufacturer cannot confirm the product was sterilized properly. The affected lots are VJ8599 (expires 09/30/2026) and VL1668 (expires 01/31/2027). No infections or injuries have been reported so far.

Moderate·FDA·Mar 25, 2026·Apotex

Sold nationwide. Somerset Therapeutics is recalling one lot of dexamethasone sodium phosphate injection because testing found impurity levels above acceptable limits as the product approached its expiration date. The affected lot (A240421, expiring 07/31/2026) was distributed nationwide. No injuries have been reported.

Moderate·FDA·Mar 25, 2026·Somerset Therapeutics

Sold nationwide. Strides Pharma Children's Ibuprofen Oral Suspension (100 mg per 5 mL) has been recalled because some bottles contain gel-like masses and black particles. The affected bottles are 4 FL OZ (120 mL) size with lot numbers 7261973A or 7261974A, expiring 01/31/2027. No injuries have been reported.

Moderate·FDA·Mar 25, 2026·Strides

Sold nationwide. Shaman Botanicals is recalling White Vein Advanced Alkaloids chewable tablets because testing found the active ingredient (7-hydroxymitragynine) is present in higher amounts than stated on the label. The label says 7.5 mg per serving, but the actual content is greater. No injuries have been reported.

Serious·FDA·Mar 25, 2026·Shaman Botanicals

Sold nationwide. One lot of Amneal Magnesium Sulfate in Water for Injection IV bags was found to contain the wrong medication—Tranexamic Acid—inside the packaging. This mix-up affects hospitals that received the product between late December 2025 and late February 2026. No patients have been harmed so far.

Serious·FDA·Mar 24, 2026·Amneal Pharmaceuticals

Sold nationwide. Aisstxoer brand adult bicycle helmets sold on Amazon do not meet safety standards for impact protection and fit stability. If you crash while wearing one, the helmet may fail to protect your head, risking serious injury or death.

Serious·CPSC·Mar 19, 2026·Yxtdz Store

Sold nationwide. The blade on Amazon Basics Camping Folding Pocket Knives can fail to stay closed, creating a risk of cuts. Amazon received one report of the blade opening unexpectedly, though no injuries have been reported so far.

Serious·CPSC·Mar 19, 2026·Amazon

Sold nationwide. Certain Frigidaire gas ranges can have a delayed ignition in the oven's bake burner, which may cause a sudden flame burst and burn injuries. About 174,800 ranges are affected, sold between June 2025 and January 2026. Electrolux Group and the CPSC have received 62 reports of delayed ignition and 30 reports of burn injuries.

Serious·CPSC·Mar 19, 2026·Electrolux

Sold nationwide. Goregent-branded infant walkers sold on Amazon can fit through standard doorways and do not stop at the edge of stairs, creating a serious fall risk. About 90 walkers with model number 901 and a yellow production label dated November 2025 are affected. No injuries have been reported yet.

Serious·CPSC·Mar 19, 2026·Goregent

Sold nationwide. BUILT brand LUUM light up tumblers can crack or break, exposing the button cell battery inside. Children can access and swallow these small batteries, which can cause serious internal burns, chemical injuries, or death. One child has already put a battery from one of these tumblers in their mouth.

Serious·CPSC·Mar 19, 2026·BUILT

Sold nationwide. Specialized electric bicycles in the Como SL line have forks that can develop small cracks over time, which may lead to fork failure and cause the rider to fall. The company has received one report of a fork failure but no injuries so far.

Serious·CPSC·Mar 19, 2026·Specialized

Sold nationwide. Tainoki Fine Furniture is recalling height-adjustable swivel office chairs sold at HomeGoods because the metal base can bend during use, creating a fall risk. The recall affects Noah, Owen, and Warren model chairs sold between August and December 2025. No injuries have been reported.

Moderate·CPSC·Mar 19, 2026·Tainoki Fine Furniture

Sold nationwide. Wagner power steamers can develop an excessively hot hose and may expel hot water during or after use, even after you release the trigger. The company has received over 50 reports of burn injuries, including first- and second-degree burns to arms, hands, feet, and faces.

Serious·CPSC·Mar 19, 2026·Wagner

Sold nationwide. Medline is recalling 2 product groups of surgical gowns and drapes, about 127,572 units in total. The fabric may separate in layers (delaminate) early when washed using the included laundering instructions. If a separated product is used during surgery and fluid passes through, there may be a risk of infection.

Moderate·FDA·Mar 18, 2026·Medline2 products

Sold nationwide. Medline and Cardinal Health have recalled specific lots of chest drainage kits used in cardiac surgery because the instructions needed to clarify that these devices are intended only for adult patients age 18 and older. The kits were distributed nationwide in California and internationally to Chile and Panama.

Moderate·FDA·Mar 18, 2026·Medline

Sold nationwide. Altruan is recalling three Strep A test products, including the Wondfo Streptococcal A At-Home Self-Test, Clearest Strep-A Cassette Test, and Bisaf Strep A Self-Test. The tests were distributed nationwide and the FDA has not cleared them. No injuries have been reported.

Moderate·FDA·Mar 18, 2026·Altruan3 products

Sold nationwide. The Lutronic CLARITY II Laser System (Model 1110200210) may spark or pop during use, potentially causing burns to patients. The FDA has identified over 1,500 affected units based on serial number.

Moderate·FDA·Mar 18, 2026·Lutronic Corporation

Sold nationwide. The Covidien HealthCast Vital Sync remote patient monitoring system has a defect that can prevent critical patient alarms from being transmitted from bedside monitors to remote monitoring stations. This means clinicians may not receive timely alerts about patient condition changes. The FDA has identified 78 affected systems.

Serious·FDA·Mar 18, 2026·Covidien LLC

Sold nationwide. International Life Sciences is recalling three Artelon FlexBand augmentation devices because they failed bacterial endotoxin testing. The recall covers three product listings and was distributed across the US and in several other countries. No injuries have been reported.

Moderate·FDA·Mar 18, 2026·International Life Sciences3 products

Sold nationwide. Beckman Coulter is recalling two clinical chemistry analyzer models, the DxC 700 AU and the AU5800, because the calibration monitor PC can show database errors if it is left open for more than 15 minutes. When this happens, the system can stop analyzing samples, which may delay test results, diagnosis, or patient treatment. No injuries have been reported.

Moderate·FDA·Mar 18, 2026·Beckman Coulter2 products

Sold nationwide. Boston Scientific is recalling certain EndoVive Safety PEG Kits that contain ChloraPrep Triple Swabsticks with open or damaged packaging. The affected swabsticks may have lost sterility or dried out. The rest of the kit components remain safe and unaffected.

Moderate·FDA·Mar 18, 2026·Boston Scientific

Sold nationwide. Medartis AG recalled specific lots of APTUS 2.5 TriLock Screws used in hand, forearm, shoulder, and foot surgery because some packages may contain 2.8mm screws instead of the labeled 2.5mm size. Using the wrong size screw could affect surgical fixation.

Moderate·FDA·Mar 18, 2026·Medartis2 products

Sold nationwide. Trividia Health is recalling the owner's booklets and instructions for use for four groups of TRUE METRIX blood glucose meters and kits. The labeling does not clearly explain that the E-5 error code can mean a very high blood glucose level or tell users to contact a healthcare professional right away. No injuries have been reported.

Serious·FDA·Mar 18, 2026·Trividia Health4 products