DC recalls

JXK Enterprises is recalling Boner Bears Chocolate (Lot #BB21125) because FDA testing found sildenafil, the active ingredient in prescription Viagra, in the product—but it was not listed on the label. Sildenafil can cause serious interactions with certain heart and blood pressure medications and poses health risks for people with diabetes, high blood pressure, or heart disease.

The LED lights inside these decorative spheres can overheat and catch fire. The company has received nine reports of sparking or overheating, though no injuries have been reported so far.

These LED shot glasses contain button cell batteries in an easily accessible compartment. Children can remove and swallow the batteries, which can cause serious internal burns and death. The glasses also lack required safety warnings.

PandaEar portable hook-on chairs have a safety defect: the crotch restraints can be removed without tools, allowing infants to fall through an opening. This violates the mandatory safety standard for these products and poses a serious injury or death risk.

ORB Toys' Funkee squeeze toys may contain asbestos-like fibers in the sand filling. If the toy ruptures or leaks, inhaling this dust could cause serious health problems. The recalled toys have date code 3102491A and were sold at Walmart and Ollie's Bargain Outlet between February 2025 and April 2026.

HomeProGym-branded resistance bands can forcefully separate from the handle during use, creating a risk of serious impact injury. The recall affects only purple 60-pound and gray 70-pound bands sold in various sets and bundles between December 2025 and April 2026. No injuries have been reported so far.

ABC Trading toy headbands and electronic pet cages contain button cell batteries in compartments that children can easily open. Swallowing these batteries can cause serious internal burns and death.

Hometown Food Company recalled a single lot of Birch Benders 12 oz Sweet Potato Pancake and Waffle Mix because it may contain undeclared egg. The affected product has lot code 5265 and a best-if-used-by date of March 24, 2027. People with egg allergies or sensitivities could have a serious reaction if they consume it.

A software issue in the A810 Clinician Programmer App can cause infusion steps to display out of order in rare cases. When this happens, the SynchroMed Flex infusion pump may not deliver medication at the intended time, or not deliver it at all. The issue affects specific clinician tablet models running software versions 1.x and 2.x.

MicroVention LVIS stent-assist devices may have incorrect dimensions or configuration due to a manufacturing mix-up. Devices that are too large can damage blood vessel walls; devices that are too small may not expand properly or could cause blood clots and stroke.

Medtronic discovered that certain lots of the Marinr Steerable reprocessed electrophysiology catheter have incomplete seals on the sterile packaging. This affects 87 units distributed in the US, Canada, and Israel. No injuries have been reported.

Stryker Sustainability Solutions is recalling Daig Livewire Steerable BDB electrophysiology catheters (Product Number 401918) due to incomplete seals on the sterile packaging. This affects 2 units with specific lot numbers. Incomplete seals may allow contamination of the sterile product.

Stryker Sustainability Solutions issued a recall of Daig Livewire Steerable reprocessed electrophysiology catheters (Product Number 401932) due to incomplete seals on the sterile packaging. The incomplete seals could potentially allow contamination of the sterile product. A total of 458 units across multiple lot numbers were affected and distributed in the US, Canada, and Israel.

Stryker Sustainability Solutions identified incomplete seals on certain lots of the Daig Livewire Steerable reprocessed electrophysiology catheter (Product Number 401923). The affected units may not maintain sterility, which could pose a risk during use. Three units have been affected.

Stryker Sustainability Solutions identified incomplete seals on certain lots of Daig Livewire Steerable electrophysiology catheters. The incomplete seals may compromise sterility of the product. Approximately 206 units across multiple lot numbers were affected.

Stryker Sustainability Solutions recalled Daig Livewire Steerable electrophysiology catheters (Product Number 401914) due to incomplete seals on the sterile packaging. The defect affects 10 units across 10 lot numbers distributed in the US, Canada, and Israel. No injuries have been reported.

Stryker Sustainability Solutions is recalling Daig Livewire Steerable electrophysiology catheters (Product Number 401908) due to incomplete seals on the sterile packaging. This affects 3 units with specific lot numbers distributed in the US, Canada, and Israel. Incomplete seals could allow contamination of the sterile product.

Stryker Sustainability Solutions is recalling certain lots of the Daig Livewire Steerable electrophysiology catheter because some units have incomplete seals on their sterile packaging. This affects 107 catheters distributed in the U.S., Canada, and Israel. No injuries have been reported.

Certain lots of the Daig Livewire Steerable electrophysiology catheter have incomplete seals on the sterile packaging. This could allow contamination of the device before use. The issue affects specific lot numbers of product number 401904.

Stryker Sustainability Solutions recalled certain reprocessed electrophysiology catheters (Daig Livewire Steerable, Product Number 401652) because the sterile packaging has incomplete seals. An incomplete seal can allow contamination to enter the package, compromising sterility before the device is used.

Stryker Sustainability Solutions identified incomplete seals on sterile packaging for certain Daig Livewire Steerable electrophysiology catheters. This affects 9 units distributed in the US, Canada, and Israel. No injuries have been reported.

Incomplete seals on sterile product

Stryker Sustainability Solutions recalled Daig Livewire Steerable electrophysiology catheters (Product Number 401581) because some units have incomplete seals on their sterile packaging. This affects 108 catheters distributed in the US, Canada, and Israel across multiple lot numbers.

Stryker Sustainability Solutions identified incomplete seals on certain lots of Daig Livewire Steerable reprocessed electrophysiology catheters. The seal defect could allow contamination of the sterile product. Affected units were distributed in the US, Canada, and Israel.

Stryker Sustainability Solutions is recalling certain lots of CS Uni-Directional electrophysiology catheters (Product Number D135304) because some units have incomplete seals on their sterile packaging. An incomplete seal could allow the sterile catheter to become contaminated before use.

Stryker Sustainability Solutions' CS Uni-Directional w Auto ID electrophysiology catheter (Product Number D135303) has incomplete seals on some units, which could compromise sterility. The affected lots were distributed in the US, Canada, and Israel. No injuries have been reported.

Stryker Sustainability Solutions is recalling certain lots of the BW Webster Duo-Decapolar reprocessed electrophysiology catheter due to incomplete seals on the sterile packaging. The incomplete seals could allow contamination of the sterile product before use. A total of 154 units were affected across the US, Canada, and Israel.

Stryker Sustainability Solutions is recalling BARD EP XT Steerable electrophysiology catheters (Product Number 200794) due to incomplete seals on the sterile packaging. The incomplete seals could allow contamination of the sterile device before use. A total of 44 units across multiple lot numbers have been affected.

Stryker Sustainability Solutions is recalling BARD EP XT Decapolar Steerable electrophysiology catheters (Product Number 201007) due to incomplete seals on the sterile packaging. The incomplete seals could allow contamination of the catheter before use. A total of 217 units across multiple lot numbers were distributed in the U.S., Israel, and Canada.

Stryker Sustainability Solutions is recalling certain reprocessed BARD Dynamic XT Steerable electrophysiology catheters due to incomplete seals on the sterile packaging. The incomplete seals may allow contamination of the sterile product before use. This affects 5 units in the US, Canada, and Israel.