Hawaii recalls

Sold nationwide. The electrical components in DIY Cold Plunge Sauna Heater Kits can overheat and create a fire hazard. The company has received 12 reports of units overheating, though no fires or injuries have occurred yet. The kits were sold online from March 2025 through February 2026.

Serious·CPSC·Mar 26, 2026·DIY Cold Plunge

Sold nationwide. FUNTOK 24V 2-Seater Ride-On Trucks (model DLS-K03) can overheat and catch fire due to a defective circuit board. The company has received 11 reports of fires, sparking, and smoking. No injuries have been reported yet, but the risk of serious burn injury is significant.

Serious·CPSC·Mar 26, 2026·Segmart

Sold nationwide. The aluminum shaft on Petzl Nomic and Ergonomic ice climbing axes can break at the handle during use, creating a fall hazard. This affects axes sold between December 2017 and March 2022. Petzl has received 26 reports of shaft breaks but no injuries so far.

Serious·CPSC·Mar 26, 2026·Petzl

Sold nationwide. CCCEI-branded power strips sold online lack proper safety protection and can overheat and catch fire if too many devices are plugged in. Two units have already sparked and melted. The company is recalling about 5,500 units sold between April 2024 and January 2026.

Serious·CPSC·Mar 26, 2026·Middle Way Electronics

Sold nationwide. GLMZZ Fidget Magnet Ball Toy Sets contain high-powered magnets that can be swallowed by children. If multiple magnets are ingested, they can attract each other inside the digestive system, causing perforations, blockages, or twisting of the intestines—which can lead to serious injury or death. The sets were sold on Amazon between February and October 2025.

Serious·CPSC·Mar 26, 2026·GLMZZ

Sold nationwide. Sunnyyes LED mini lights contain lithium coin batteries that children can easily access and swallow. The battery compartment screws can come loose, and the packaging lacks required safety warnings. Swallowing these batteries can cause serious internal burns and death.

Serious·CPSC·Mar 26, 2026·Sunnyyes

Sold nationwide. DuraTrac stainless steel gas connectors sold between May and November 2025 contain a manufacturing defect that can cause gas leaks. These leaks pose a fire hazard. About 196,800 units are affected.

Serious·CPSC·Mar 26, 2026·DuraTrac

Sold nationwide. AirClub convertible bassinets (model QX-831) have a defective attachment mechanism that creates a dangerous gap between the bassinet and adult bed mattress. Infants can fall through this opening, causing serious injury or death. About 110,400 units were sold online between October 2023 and December 2025.

Serious·CPSC·Mar 26, 2026·AirClub

Sold nationwide. Vive Health bed rails can trap users between the rail and mattress, creating a serious risk of asphyxiation. Two deaths have been reported. The recall affects three models: Compact Bed Rail (LVA2009SLV), Bed Rail Collection V (LVA2097SLV), and Bed Rail model LVA1024 purchased on or before August 21, 2023.

Serious·CPSC·Mar 26, 2026·Vive Health

Sold nationwide. 4our Kiddies plastic furniture straps (tip restraint kits) can break or degrade over time, allowing furniture to tip over and potentially trap or injure children or elderly people. The plastic brackets and cables fail to meet safety standards, and CPSC has received reports of at least 150 incidents where these straps broke, including three furniture tip-overs.

Serious·CPSC·Mar 26, 2026·4our Kiddies

Sold nationwide. Nexgrill grill brushes sold at Home Depot can shed small metal wire bristles that may stick to food or the grill surface. If swallowed, these bristles can cause serious internal injuries requiring surgery. The company has identified at least 68 cases where bristles detached, including five people who needed medical care.

Serious·CPSC·Mar 26, 2026·Nexgrill

Sold nationwide. Datascope's Battery Charging Station (Model 0998-00-0802) for Cardiosave IABP batteries has a protruding screw in the left bay that can prevent certain batteries from inserting fully and charging properly. The right bay works normally. This affects 28 units distributed in select U.S. states and international locations.

FDA·Mar 25, 2026·Datascope

Sold nationwide. Hologic's Aptima HPV Assay test kits (Master Lot 929785) may produce invalid results or false negatives, meaning they could fail to detect HPV infection. The affected kits were distributed to healthcare facilities in California, Florida, Iowa, Illinois, Missouri, North Carolina, New Mexico, Puerto Rico, and Tennessee.

Moderate·FDA·Mar 25, 2026·Hologic

Sold nationwide. Diagnostica Stago's STA Liatest D-Di blood test kits are giving inaccurate measurements for D-dimer (a marker used to help rule out blood clots). The kits are showing higher-than-actual results across all test ranges. These kits are used in hospital and reference laboratories on specific analyzer machines.

Moderate·FDA·Mar 25, 2026·Diagnostica Stago

Sold nationwide. ConvaTec's EsteemBody Drainable Pouch (model REF:423643, 10–45mm) may leak because of a manufacturing issue. The affected pouches have lot numbers 5K00011 or 5K00714 and have been distributed worldwide. No injuries have been reported.

Moderate·FDA·Mar 25, 2026·ConvaTec3 products

Sold nationwide. Elekta has recalled certain Leksell Gamma Knife Perfexion and Icon radiosurgery systems because an adapter component may not be properly aligned or locked in place. This could affect the accuracy of radiation delivery during treatment. No injuries have been reported.

Moderate·FDA·Mar 25, 2026·Elekta

Sold nationwide. Some Stryker Cub Pediatric Cribs sold in the USA are missing two warning labels on the access doors. This affects 590 cribs with specific serial numbers. No injuries have been reported.

Moderate·FDA·Mar 25, 2026·Stryker

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

Winder Laboratories is recalling certain batches of their grape-flavored multivitamin with fluoride chewable tablets because they contain less vitamin D than stated on the label. The FDA discovered this during an inspection. The affected products are the 0.25 mg and 1 mg formulations with specific lot numbers and expiration dates in October and November 2025.

Moderate·FDA·Mar 25, 2026·Winder Laboratories

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