Check a product

Medline recalled 15 medical procedure convenience kits that contain MASTISOL liquid adhesive. Complaints reported that the butyrate tubing cracked when the adhesive vials were activated. No injuries have been reported.

Moderate·FDA·Feb 4, 202615 products

NIPRO Technical Services' Conductivity Standard Solutions (models 10001, 10011, 10021, 10032, 10040, 10040c, 10041) have a defect that causes incorrect conductivity readings. These solutions are used to calibrate meters that measure dialysate (the fluid used in dialysis treatment). If calibration is inaccurate, dialysis machines may report wrong conductivity values, which could affect treatment safety.

Moderate·FDA·Feb 4, 2026

Gold Star Distribution is recalling five product listings, including first aid kits, condoms, feminine hygiene products, toothbrushes and toothpaste, and pregnancy tests. The recall was issued because of potential exposure to rodents and signs of rodent activity at its distribution center. The products were distributed nationwide, including in Minnesota, and no injuries have been reported.

Moderate·FDA·Feb 4, 20265 products

Fixing screws in the ceiling-mounted arm of Canon Medical's Alphenix INFX-8000C interventional X-ray systems may become loose. This can cause the ceiling arm to stop moving sideways, create unusual noises, or trigger sensor errors during use.

Moderate·FDA·Feb 4, 20264 products

Certain Siemens interventional X-ray systems with software version VB10D-SP02 have a software issue that can cause images to display incorrectly. When the automatic image-flip feature is used, images may not flip as expected, and in some cases, a previous patient's image could appear instead of the current patient's image.

Moderate·FDA·Feb 4, 20262 products

Aju Pharm is recalling 8 suture anchor products, about 6,669 units in total, because of reports that anchors can break, bend, or pull out, and that sutures and secondary packaging can break. No injuries have been reported. The recall covers the Fixone, Genesis, and AlternatiV+ anchor lines.

Moderate·FDA·Feb 4, 2026·Aju Pharm8 products

Cerapedics recalled PearMatrix P-15 Peptide Enhanced Bone Graft (1.0cc) due to an incorrect expiration date on certain units. The affected lot is 7014819. No injuries have been reported.

Moderate·FDA·Feb 4, 2026·Cerapedics

Elekta medical linear accelerators used in cancer radiation therapy have a manufacturing defect affecting electrical grounding in certain models and lot codes. The issue could potentially affect the safe operation of these systems. No injuries have been reported to date.

Moderate·FDA·Feb 4, 2026

Qunol Extra Strength Turmeric Capsules (1000mg) in 60-count and 120-count bottles have been recalled due to mold contamination in raw materials used to make the product. The contamination was found in material lots produced in July. No injuries have been reported.

Moderate·FDA·Feb 4, 2026·Qunol

Novadoz Pharmaceuticals is recalling specific lots of glycopyrrolate oral solution (1 mg/5 mL) because the medication failed quality testing for impurities and degradation. The affected lots may not meet safety and effectiveness standards. Three lots are involved, with expiration dates between April and May 2027.

Moderate·FDA·Feb 4, 2026·Novadoz

Greenstone LLC is recalling methylprednisolone 4 mg Dosepak tablets (Lot #LG7675, expiring November 2026) because the blister foil is oriented incorrectly. This misalignment can make the dosing directions on the foil confusing or unclear, which could lead to taking the wrong dose.

Moderate·FDA·Feb 4, 2026·Greenstone

Some bottles of INON ACE antacid tablets are dissolving more slowly than they should in your stomach. This means the medication may not work as intended. The affected bottles were distributed in California and Hawaii.

Moderate·FDA·Feb 4, 2026·Sato Pharmaceutical

Baxter Healthcare's Sterile Water for Irrigation 250 mL bottles may contain small plastic particles that came loose from the bottle rim and entered the solution. This affects lot G171359 with an expiration date of 05/31/2027. No injuries have been reported.

Moderate·FDA·Feb 4, 2026

Philips released a software update (version 4.5.0) for the Patient Information Center iX that changes how mobile event notifications are filtered. The system makes these changes without alerting users, so staff may not realize their notification settings have been altered.

Moderate·FDA·Jan 28, 2026

Edan Diagnostics is recalling 16 EDAN medical monitoring products after receiving an FDA letter about possible cybersecurity issues. The products include fetal and maternal monitors, vital signs monitors, patient monitors, a central monitoring system, and a telemetry transmitter. No injuries have been reported.

Moderate·FDA·Jan 28, 2026·Edan Diagnostics16 products

Community Products is recalling three Rifton Equipment models, the TRAM (K310), Low Base TRAM (K320), and E-Pacer (K660), because the body support strap may fray. The recall covers about 4,800 units and was distributed in the US and several other countries. No injuries have been reported.

Moderate·FDA·Jan 28, 2026·Community Products3 products

Sysmex America's TS-10/TS-10H Tube Sorter may experience an unexpected loss of electromagnetic holding force in the lift mechanism under certain conditions. This could cause the lift to move downward unintentionally. The issue affects 44 specific units identified by serial number.

Moderate·FDA·Jan 28, 2026·Sysmex

Beckman Coulter's LDL Cholesterol OSR6x96 reagent may give inaccurate test results when patients have high triglyceride levels (above 1500 mg/dL). The test can overestimate LDL cholesterol by up to 29% in some samples, which could affect patient care decisions.

Moderate·FDA·Jan 28, 2026

Intuitive Surgical has recalled certain Ion Vision Probe Bags (model 490127) because the sterile pouch seal may be compromised or incomplete. These bags are used to store the Vision Probe during lung biopsy procedures. A compromised seal could allow contamination of the sterile device.

Moderate·FDA·Jan 28, 2026

MicroPort Orthopedics distributed a hip implant trial component (HIPTURN FEM HEAD TRIAL 36MM) in the United States without FDA premarket authorization. The company sent approximately 91 units to distributors across multiple states. No injuries have been reported.

Moderate·FDA·Jan 28, 2026·MicroPort Orthopedics

Tyber Medical is recalling two sizes of left distal radius plates from its VOLT Wrist Treatment System, 164 units in total. The supplier made the plates with threads facing the wrong direction. No injuries have been reported.

Moderate·FDA·Jan 28, 2026·Tyber Medical2 products

Two Leaseir MHR Xcell surgical lasers used for hair removal and skin treatment were distributed with console labels missing the required "DANGER" symbol. The missing warning label could prevent users from recognizing laser hazard warnings. No injuries have been reported.

Moderate·FDA·Jan 28, 2026·Leaseir Technologies

Merit Medical is recalling seven inflation devices and kits, including Allwell and Merit Medical products. The inflation device handle may detach from the syringe during a procedure. No injuries have been reported.

Moderate·FDA·Jan 28, 20267 products

Philips has identified two software issues in Azurion R3.1 systems that may cause the device to restart continuously, lose X-ray imaging capability, lose motorized movement, display incorrect images, or lose data. One issue affects all models; a second affects only systems with a Poly-G3 frontal stand.

Moderate·FDA·Jan 28, 2026

RaySearch Laboratories is recalling nine RayStation and RayPlan radiation therapy treatment planning software entries. Certain regions of interest with no contours, which have a material override or are of type Bolus, Fixation, or Support, may not invalidate calculated radiation dose as intended when their geometry is changed or their material override is removed. No injuries have been reported.

Moderate·FDA·Jan 28, 2026·Raysearch Laboratories9 products

Zydus Pharmaceuticals is recalling Icosapent Ethyl 1-gram capsules because some bottles may contain capsules that have lost potency (strength) due to leakage and oxidation. This means the medication may not work as intended. The recall affects specific lot numbers expiring in February and April 2027.

Moderate·FDA·Jan 28, 2026

Specialty Process Labs is recalling one lot of Thyroid, USP (an active pharmaceutical ingredient used in manufacturing) because it does not meet strength standards. The affected lot may contain less active ingredient than labeled, which could affect the potency of products made with it.

Moderate·FDA·Jan 28, 2026·Specialty Process Labs

Rising Pharmaceuticals is recalling Furosemide Tablets, USP 40 mg (a water pill used to treat swelling and high blood pressure) because some bottles may contain a foreign substance. The affected lot is FUB125042G with an expiration date of May 2027. This recall affects 4,212 bottles distributed nationwide.

Moderate·FDA·Jan 28, 2026·Graviti Pharmaceuticals

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

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