Check a product

Rheumacare capsules manufactured by Virgo UAP Pharma in India were found to contain lead due to manufacturing defects. The affected product is a 30-count bottle with lot numbers CAM040 (expires 06/30/2029) or CAL079-N (expires 09/30/2028). Only 4 bottles were distributed to a customer in New York.

Serious·FDA·Feb 11, 2026

Granules Pharmaceuticals is recalling certain bottles of trazodone 50 mg because some bottles may contain foreign tablets or capsules mixed in. This affects 71,424 bottles with batch number 6160008A and an expiration date of 12/31/2026. No injuries have been reported.

Moderate·FDA·Feb 11, 2026·Granules

Green Lumber Natural Fuel For Men capsules were sold as a supplement but contain tadalafil, a prescription medication approved only for treating erectile dysfunction and certain heart conditions. The product was marketed and sold without FDA approval and without listing tadalafil on the label. Tadalafil can cause serious side effects, especially in people taking certain other medications or with certain health conditions.

Serious·FDA·Feb 11, 2026

Unichem Pharmaceuticals is recalling one lot of bisoprolol fumarate and hydrochlorothiazide tablets (2.5 mg/6.25 mg) because they contain higher-than-allowed levels of N-Nitroso Bisoprolol, a potentially harmful impurity. The affected lot was manufactured in India and distributed nationwide.

Moderate·FDA·Feb 11, 2026·Unichem Pharmaceuticals

Miach Orthopaedics BEAR Implant Model 1000 units have an incorrect expiration date printed on the label that extends beyond the product's actual shelf life. Because the expiration date is wrong, the UDI (Unique Device Identifier) is also incorrect. This affects 284 units distributed nationwide.

Moderate·FDA·Feb 4, 2026·Miach Orthopaedics

LSL Healthcare's Central Line Dressing Kit (Model 2519CP) contains BD ChloraPrep Triple Swabsticks with damaged packaging—some applicator seals are open. An open seal can allow the sterile applicator to become contaminated before use. This affects about 1,400 kits distributed in Idaho with lot number 5G3119 and expiration date 7/31/26.

Moderate·FDA·Feb 4, 2026·LSL Healthcare

LimFlow Vector vascular devices (Model VT-US-23, Lot 82321838) were distributed with an incorrect expiration date printed on the packaging. This affects 33 units distributed across multiple U.S. states. An incorrect expiration date could lead to use of a device beyond its safe lifespan.

Moderate·FDA·Feb 4, 2026·LimFlow

Some BD Alaris Pump Module 8100 infusion pumps have a software date/time issue related to daylight saving time that may prevent them from connecting to hospital networks. This affects only the network connectivity function; the pump's ability to deliver medication is not impacted. The issue involves 189 devices distributed in Arizona, Indiana, Ohio, and Virginia.

Moderate·FDA·Feb 4, 2026

Philips is recalling 13 MR imaging system products because exported MR Elastography stiffness maps may show incorrect stiffness values when viewed in a PACS image viewer. No injuries have been reported.

Moderate·FDA·Feb 4, 202613 products

The screen on Zimmer A.T.S. 5000TS Tourniquet Systems may freeze or stop responding when used in certain non-English language settings. This can delay surgery while staff locate an alternate device. The issue affects systems running software version v2.04 or earlier.

Moderate·FDA·Feb 4, 20262 products

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

SunMed is recalling four Broselow pediatric emergency products, including Rainbow Tapes and ALS organizers, because they may contain dosing errors for the drugs vecuronium, flumazenil, and ketamine. The FDA has classified this as a Class I recall, its most serious category. The products were distributed in the US nationwide, Canada, Hong Kong, and Singapore, and no injuries have been reported.

Serious·FDA·Feb 4, 2026·SunMed4 products

Superfoods is recalling two Live it Up Super Greens whole food supplement powders, one plain and one Natural Wild Berry flavor, both sold in 30-day supplies (8.5 oz). The products may be contaminated with Salmonella Typhimurium. They were distributed nationwide, including Puerto Rico, Guam, the Virgin Islands, and the United Kingdom, and no illnesses have been reported.

Serious·FDA·Feb 4, 20262 products

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

Some bottles of Parodontax Active Gum Health mouthwash (mint, 16.9 FL OZ) may be missing or have illegible lot and expiration date codes. This makes it impossible to know when the product expires. The affected lot is #0665363 with an expiration date of 08/31/2027.

FDA·Feb 4, 2026

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

GVS released 2,720 SQ40S blood transfusion filters without completing required quality control testing. Because the sterility verification process was not finished, the company cannot confirm these filters are safe to use. The affected lot number is 7536142.

Serious·FDA·Jan 28, 2026·GVS

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