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SiluetaYa Mexican Tejocote Roots Supplement Pieces contain yellow oleander, a toxic plant that can cause serious illness. The affected product was sold online in Arizona, California, New Mexico, New York, Texas, and Utah. This is a Class I recall, the FDA's most serious category.

Serious·FDA·Apr 1, 2026

Teva Pharmaceuticals is recalling specific lots of Octreotide Acetate 30 mg injectable suspension due to quality control problems found at the manufacturer. The FDA identified deficiencies that mean the sterility of these vials cannot be guaranteed. No injuries have been reported.

Serious·FDA·Apr 1, 20263 products

Certain versions of GE Centricity Universal Viewer software (versions 6.0 through 6.0 Sp10.4.1) contain a cybersecurity vulnerability that may expose user login credentials on affected workstations. An unauthorized person could potentially access the system and interfere with medical imaging data or system availability.

Serious·FDA·Mar 25, 20263 products

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

The Covidien HealthCast Vital Sync remote patient monitoring system has a defect that can prevent critical patient alarms from being transmitted from bedside monitors to remote monitoring stations. This means clinicians may not receive timely alerts about patient condition changes. The FDA has identified 78 affected systems.

Serious·FDA·Mar 18, 2026

International Life Sciences is recalling Artelon FlexBand Plus augmentation devices (Ref: 41054 and 41057) because they failed bacterial endotoxin testing. These devices may contain harmful bacterial contamination that could cause infection or other complications if implanted.

Serious·FDA·Mar 18, 2026·International Life Sciences3 products

The instruction manuals for TRUE METRIX AIR blood glucose meters sold at Walgreens, CVS, Walmart, and other retailers don't clearly explain what the E-5 error code means or what to do about it. An E-5 error can signal a dangerously high blood glucose level, but the current instructions don't emphasize this or tell you to contact a doctor right away.

Serious·FDA·Mar 18, 2026·Trividia Health4 products

Rosabella brand moringa dietary supplement capsules distributed by Ambrosia Brands LLC may be contaminated with Salmonella, a bacteria that can cause serious illness. The recall affects multiple lots with expiration dates ranging from March 2027 through November 2027. This product was sold nationwide and internationally.

Serious·FDA·Mar 18, 2026

Staar Surgical EVO+ Visian Toric Implantable Collamer Lenses (Model VTICM5) were labeled as 12.1 mm but are actually 12.6 mm in length. The larger size can cause the lens to sit too high in the eye, potentially reducing eye drainage and increasing eye pressure, which may lead to discomfort, vision problems, or the need for lens removal.

Serious·FDA·Mar 11, 2026·Staar Surgical

GE Healthcare has identified a software issue in certain versions of its Centricity Universal Viewer Zero Footprint Client where patient information displayed in the viewer may not match the medical images being shown. This could occur in specific workflows on systems with Patient Timeline installed. The issue affects approximately 250 units.

Serious·FDA·Mar 11, 2026

Abiomed is recalling three Impella RP heart pump models because the differential pressure (dP) sensor may malfunction and its readings may drift. The recall covers 4,966 units in total and was distributed in the US and several other countries. No injuries have been reported.

Serious·FDA·Mar 11, 20263 products

Medline dialysis on/off kits may contain Tego Connectors with defective silicone seals that can dome or tear. This can block the fluid path, prevent blood product injection or withdrawal, cause fluid leakage, delay treatment, or allow air or contaminants into the body.

Serious·FDA·Mar 4, 20266 products

Medline Industries is recalling 23 models of IV administration and extension sets because the male connectors may leak, crack, or break during use under certain conditions. This could cause delays in treatment, blood loss, infection, air embolism, or patients not receiving the correct medication dose.

Serious·FDA·Feb 25, 2026

Olympus Corporation is recalling the High Flow Insufflation Unit (Model UHI) used during abdominal surgery due to a software problem that may cause overpressure events. The device is used to inflate the abdominal cavity and remove smoke during laparoscopic surgery. No injuries have been reported.

Serious·FDA·Feb 25, 20263 products

Why Not Natural Moringa Capsules (lot #A25G051, expiration 07/2028) may be contaminated with Salmonella, a bacteria that can cause serious illness. The affected capsules were distributed nationwide. No illnesses have been reported so far.

Serious·FDA·Feb 25, 2026

Certain da Vinci 5 Surgeon Console Viewer Displays have outdated firmware that may cause loss of the 3D surgical display or both displays entirely during surgery. When this happens, the surgical instruments remain active even though the surgeon cannot see the surgical field, which could result in unintended tissue contact, bleeding, or injury.

Serious·FDA·Feb 18, 2026

Elekta's Leksell GammaPlan software version 11.1 has a bug that can cause incorrect radiation targeting during Gamma Knife treatment planning. If users don't update an old reference point before creating a new treatment plan, the radiation may be aimed at the wrong location. This error may not be caught during normal review.

Serious·FDA·Feb 18, 20262 products

Medline is recalling seven groups of reprocessed heart and ultrasound catheters because they may contain small particles of leftover material. If these devices are used, the particles could cause inflammation, infection, or blood clots, which may lead to embolism or deep vein thrombosis. This is an expansion of an earlier recall, and the affected catheters were distributed nationwide.

Serious·FDA·Feb 18, 20267 products

Medline is recalling two suction catheter kit products, with about 142,100 units affected. Some kits may contain an 8 Fr suction catheter instead of the required 14 Fr catheter. Using the smaller catheter could partly or fully block the airway and reduce oxygen. No injuries have been reported.

Serious·FDA·Feb 18, 20262 products

McKesson's UDENYCA (pegfilgrastim-cbqv) injection was stored at room temperature instead of in the refrigerator, which may have reduced its effectiveness. This affected 116 cartons from Lot 2199821 with specific serial numbers. The FDA classified this as a Class I recall.

Serious·FDA·Feb 18, 2026·McKesson

Fresenius Kabi is recalling five premixed IV bags labeled Fagron Sterile Services in Canton, MA: acyclovir, ketamine, thiamine, and two strengths of vancomycin. The company cannot assure the bags are sterile. No injuries have been reported.

Serious·FDA·Feb 18, 20265 products

Vortex Surgical Inc. is recalling certain 25GA Subretinal Injection Cannula (model VS0220.25, Lot 2410043) because the sterile Tyvek pouches may have small voids or gaps in the seal. If a pouch is compromised, the cannula inside is no longer sterile and could become contaminated with bacteria, risking infection during eye surgery.

Serious·FDA·Feb 11, 2026·Vortex Surgical13 products

Some Medtronic MiniMed 780G insulin pumps with software version 6.60 may experience a software timing issue that triggers an error code and stops insulin delivery. This affects specific catalog numbers (MMT-1884, MMT-1886) with certain serial numbers.

Serious·FDA·Feb 11, 2026

Boston Scientific is recalling six versions of its AXIOS Stent and Electrocautery-Enhanced Delivery System after reports that the stent did not deploy or expand properly. The most likely result is a longer procedure while the device is swapped for a new one. In rare cases, the stent may need to be removed through a second endoscopic or surgical procedure. No injuries have been reported.

Serious·FDA·Feb 11, 20266 products

Diva Fam Inc's Wildcrafted Sea Moss Gel Superfood may be contaminated with Clostridium botulinum, a bacterium that produces a dangerous toxin. The affected product is sold nationwide in glass jars (16 fl oz) with specific lot codes. No illnesses have been reported so far.

Serious·FDA·Feb 11, 2026·Diva Fam14 products

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

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

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

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