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Cipla USA is recalling Diclofenac Sodium Topical Gel 1% (batch XHBG, expiring 08/31/2027) because it failed to meet required pH specifications during quality testing. The gel may not work as intended or could cause skin irritation. No injuries have been reported so far.

Moderate·FDA·Jan 28, 2026

Academy Sports + Outdoors is recalling Magellan Odyssey Rocker Chairs sold between September and October 2025 because the chair legs can break. This poses a risk of falls and injury. The chairs have a metal frame with mesh backrest and were sold in charcoal, navy, olive green, and teal colors.

Moderate·CPSC·Jan 22, 2026

Angry Orange Enzyme Stain Remover products may contain Pseudomonas aeruginosa bacteria, which can cause serious infections in people with weakened immune systems, lung conditions, or external medical devices. The bacteria can enter the body through inhalation, eyes, or breaks in the skin. People with healthy immune systems are typically not at risk.

Moderate·CPSC·Jan 22, 2026·Thrasio

ICU Medical is recalling two products, the Pulsator Arterial Blood Sampling Kit and the Portex Spinal Tray, with 64,290 affected units each. Some syringes may have a crack on the syringe collar, which can cause delayed or repeated blood draws or fluid delivery, and blood leakage during arterial sampling or fluid delivery. No injuries have been reported.

Moderate·FDA·Jan 21, 20262 products

Medtronic has recalled certain Abre Venous Self-Expanding Stents due to a manufacturing issue with the stent material (Nitinol) that can cause the stent to be smaller than intended when deployed. This reduced size may result in the stent moving out of position after placement.

Moderate·FDA·Jan 21, 2026

Intuitive Surgical is recalling certain da Vinci SP Access Port Kits because the sterile trays may develop cracks during storage or handling. A cracked tray could allow bacteria or other contaminants to enter, compromising the sterile field during surgery. No injuries have been reported.

Moderate·FDA·Jan 21, 2026

Instrumentation Laboratory has recalled a coagulation test reagent (Part Number 0020006800, Lot N1136730) used to evaluate blood clotting and monitor heparin therapy due to potential microbial contamination. The affected lot expires 12/31/2025 and was distributed worldwide including multiple U.S. states and countries. No injuries have been reported to date.

Moderate·FDA·Jan 21, 2026

Hologic's ThinPrep CytoLyt Solution (a buffered cell wash used in laboratory testing) from lot number 5062EC has been found to contain fungal contamination. The affected product was distributed nationwide. No injuries have been reported.

Moderate·FDA·Jan 21, 2026

Philips Azurion X-ray imaging systems running software versions R2.1.10 or R2.2.10 may experience six different software problems. These include unexpected system restarts, continuous restart loops, storage space issues, and positioning errors that could affect image quality or system availability.

Moderate·FDA·Jan 21, 2026

Medline is recalling six groups of surgical convenience kits, about 59,000 units in total, that include Stryker Strykeflow 2 Suction Irrigators. A 2024 design change lets irrigation solution reach the handpiece and battery pack, which can cause the device to leak or give off vaporized saline that may look like smoke. No injuries have been reported.

Moderate·FDA·Jan 21, 20266 products

Diagnostica Stago is recalling lot 271288 of the Asserachrom HPIA test kit, which detects antibodies related to heparin-induced thrombocytopenia (HIT type II). The affected lot may have defective test wells that produce false negative results, meaning the test could fail to detect the condition when it is present.

Moderate·FDA·Jan 21, 2026

Heraeus is recalling four PALACOS bone cement products sold in 17 countries outside the US. Some ampoules may not break during mixing, so no usable cement forms and the product cannot be used on a patient. No injuries have been reported.

Moderate·FDA·Jan 21, 2026·Heraeus4 products

Philips is recalling 16 Allura Xper imaging system models because a drip tray under the cooling unit may not have been installed during earlier field corrections, or the installation was not properly documented. Without the tray, coolant could reach electrical components, possibly causing short-circuits, blown fuses, or system shutdown. No injuries have been reported.

Moderate·FDA·Jan 21, 202616 products

BD Ready-to-Use Hydrophilic Catheters (14 Fr, straight tip, model RTU14F) distributed in Georgia have an incorrect expiration date printed on the label. This labeling error means the actual shelf life of the product may differ from what is shown. No injuries have been reported.

Moderate·FDA·Jan 21, 2026·Bever

Medline is recalling 12 kits that contain B. Braun IV administration sets and pump administration sets. Customers reported that the check valve components in these sets can get stuck in the open or closed position. No injuries have been reported.

Moderate·FDA·Jan 21, 202612 products

Fresenius Kabi is issuing a recall for the Ivenix Infusion System (IIS) with LVP Software version 5.10.2 and earlier. The manufacturer is emphasizing instructions for LVP duration programming in the device manual to ensure proper use. No injuries have been reported.

Moderate·FDA·Jan 21, 2026

GE HealthCare discovered that certain older SMV DSI nuclear medicine systems may have been moved or transported without proper detector support. This can stress the detector mounting and potentially cause the detector to fall, which could injure someone. No falls or injuries have occurred yet.

Moderate·FDA·Jan 21, 20264 products

The Vanta A71200 Clinician Programmer App (versions 2.0.2465 and 2.0.2683) running on Samsung tablets may not work properly during use. This malfunction could delay or postpone surgical procedures. The implanted neurostimulator devices themselves are not affected—only the programming software.

Moderate·FDA·Jan 21, 2026·Medtronic Neuromodulation

Boston Scientific found that certain batches of Coyote Over-the-Wire PTA Balloon Dilation Catheters may not inflate or deflate properly during use due to a manufacturing process variation. The issue affects only catheters made between September 12 and October 13, 2025. The company has corrected the manufacturing process.

Moderate·FDA·Jan 21, 2026

Mobius Imaging is recalling two products for the AIRO Computed Tomography (CT) X-ray System: a replacement pendant component and a pendant upgrade component. The pendants do not have the required "Safe Hand Position Warning" label. No injuries have been reported.

Moderate·FDA·Jan 21, 2026·Mobius Imaging2 products

Medicrea is recalling two IB3D surgical products, the Universal Implant Inserter and the PL Instruments Set, because the rotation tool handle may separate from its shaft. If that happens, the surgeon may be unable to rotate the implant. The company reports 44 units of each product affected, and no injuries have been reported.

Moderate·FDA·Jan 21, 2026·Medicrea2 products

Repligen is recalling the MAVERICK Measurement Module Spectrometer due to cable connection defects that can cause two problems: the laser output may increase to unsafe levels, or the laser may fire unexpectedly during normal operation. A loose or poorly crimped cable under stress can trigger these faults. No injuries have been reported.

Moderate·FDA·Jan 21, 2026

Ice can form in the venting system of Canon Medical VANTAGE TITAN 3T MRI machines (models MRT-3010/MEXL-3010). If the system undergoes a quench event while ice is present, helium gas may not escape properly and pressure inside the helium vessel could build up and rupture, releasing helium gas into the scanning room.

Moderate·FDA·Jan 21, 20262 products

AZ Gems Jumbo Raw Shrimp (2 lb bags, UPC 1 93968 00697 6) contains elevated levels of chloramphenicol, an antibiotic not approved for use in the U.S. food supply. The affected product was distributed nationwide under the Member's Mark label. No illnesses have been reported to date.

Moderate·FDA·Jan 21, 2026·Member's Mark

So Delicious Dairy Free Salted Caramel Cluster Cashewmilk non-dairy frozen dessert may contain foreign material. The recall affects specific batches distributed across the US and Canada. No injuries have been reported.

Moderate·FDA·Jan 21, 2026·So Delicious Dairy Free

Ukrop's is recalling three sizes and icing styles of its 6-inch and 8-inch pound cakes with buttercream icing, including confetti and pink or red roses. The labels do not list soy, but soy was used in the cakes. The cakes were shipped to Virginia and West Virginia. No illnesses have been reported.

Moderate·FDA·Jan 21, 20263 products

Sanders Candy Factory Inc. is recalling frosted almonds (bulk product code 23208, lot codes 058.25 and 070.25) due to elevated levels of aflatoxin, a naturally occurring toxin that can cause serious health problems. The affected product was identified before it reached consumers and was only distributed to a commercial customer.

Moderate·FDA·Jan 21, 2026

Gusto is recalling two sizes of Klong Kone shrimp paste, sold in plastic jars, after testing found high lead levels. The recall covers a 16 oz size and a 32 oz size, with 7 cases of each affected. The products were distributed in Iowa and New Jersey, and no injuries have been reported.

Moderate·FDA·Jan 21, 20262 products

Eureka Inc cinnamon in 100g clear plastic containers has been found to contain elevated levels of lead. The affected product has Batch No. 06 B:02 with a best-by date of May 2026. The contaminated cinnamon was distributed to retailers and wholesalers in California and Michigan.

Moderate·FDA·Jan 21, 2026

Mangalm is recalling two Tops jams: Tops Strawberry Jam and Tops Mixed Fruit Jam. The recall is due to an unapproved color, carmoisine. The products were distributed in California. No injuries have been reported.

Moderate·FDA·Jan 21, 2026·Tops2 products