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Breckenridge is recalling two sizes of duloxetine delayed-release capsules, 30 mg and 60 mg, made by Towa Pharmaceutical Europe in Spain. The recall covers about 374,400 bottles distributed nationwide. The capsules contain an impurity called N-nitroso-duloxetine at a level above the FDA's recommended interim limit. No injuries have been reported.

Moderate·FDA·Jun 17, 20262 products

Fresenius Kabi USA is recalling specific batches of epinephrine injection due to failed impurity and degradation specifications. The affected vials may not meet required purity standards. No injuries have been reported.

Moderate·FDA·Jun 17, 2026

Sun Pharmaceutical's doxorubicin hydrochloride liposome injection vials were found to contain glass particles. The affected vials are lot HAG2581B, which expire in May 2027. About 675 vials were distributed nationwide.

Serious·FDA·Jun 17, 2026

Beekeeper's Naturals Saline Nasal Spray was manufactured without proper sterilization, allowing microbial contamination. The affected product is Lot #5950 with an expiration date of 02/2028. No injuries have been reported so far.

Moderate·FDA·Jun 17, 2026·Beekeeper's Naturals

Sensory Supplement LLC is recalling Neuro Nourish dietary supplement due to premature lipid oxidation that can cause an off odor and bitter taste. The affected product is a 5.9 oz multi-nutrient supplement sold online nationwide. No injuries have been reported.

FDA·Jun 17, 2026·Neuro Nourish2 products

Beekeeper's Naturals is recalling one lot of its Saline Nasal Spray sold on Amazon because it contains elevated levels of yeast and may be contaminated with Aspergillus, a fungus that can cause serious infections in people with weakened immune systems or lung disease. The company has received four reports of sinus congestion, irritation, or infection potentially linked to this product.

Serious·FDA·Jun 11, 2026·Beekeeper's Naturals

Sato Pharmaceutical's Yunker Energy & Health Herbal Supplement with Vitamins does not contain the amount of Vitamin E stated on its label. The affected product was distributed nationwide through two domestic distributors. No injuries have been reported.

FDA·Jun 10, 2026·Yunker

Some Medline EYE TRAY-LF convenience kits (SKU DYNJ21627P) contain syringes labeled as tuberculin syringes on the box, but the actual syringes inside are insulin syringes. Using the wrong syringe type could lead to incorrect dosing.

Moderate·FDA·Jun 3, 2026

Philips is recalling Azurion and Allura imaging systems because the hard drives in their PCs may slow down as they age, especially after six years of use. Depending on the system, this can cause loss of imaging function, and in Allura systems it may also cause loss of motorized movement or data loss. A system restart may temporarily restore function. No injuries have been reported, and the recall covers 2 product lines with about 3,069 affected units.

Moderate·FDA·Jun 3, 20262 products

GE HealthCare recalled six ApexPro CARESCAPE Telemetry Server products and related software. A persistent NO COMM or OFF NETWORK condition at the Central Station could cause loss of ECG and SpO2 monitoring. No injuries have been reported.

Serious·FDA·Jun 3, 20266 products

A limited number of Medtronic 1x4 Pocket Adaptor Kits (Models 64001 and 64002) used in deep brain stimulation devices are labeled with incorrect Use-By-Dates. The mislabeled kits may no longer be safe or effective for their intended use.

Moderate·FDA·Jun 3, 20262 products

Devicor Medical Products is recalling HydroMARK Breast Biopsy Site Marker Model 4010-02-15-T3 due to incorrect labeling on individual packages inside boxes. Some boxes labeled as T3 markers may contain packages labeled as T4 markers, which could lead to use of the wrong marker type during a breast biopsy procedure.

Moderate·FDA·Jun 3, 2026·Devicor

Certain Impella Controller (AIC) consoles contain electrical faults including alarm failures, power-path problems, and inaccurate motor sensing. Additionally, improper alignment between the purge cassette and motor drive can prevent the purge system from priming correctly, requiring users to switch to a backup console.

Serious·FDA·Jun 3, 2026

Medline is recalling seven procedure kit products that contain bupivacaine hydrochloride in dextrose injection made by Huons Co. That bupivacaine was itself recalled over quality problems, including questions about microbiology testing data and reports of reduced effectiveness. No injuries have been reported.

Serious·FDA·Jun 3, 20267 products

Halyard Purezero Ultraviolet Nitrile Exam Gloves in sizes XS through XL failed to meet chemical permeation performance standards, meaning they may not provide adequate protection against certain chemicals. This affects approximately 452,500 units distributed nationwide.

Moderate·FDA·Jun 3, 2026·Halyard

Abiomed identified that certain Automated Impella Controller (AIC) units have internal hardware issues that could affect device operation. These include cable and component positioning problems that may interrupt motor controls, cause startup failures, or prevent the device from booting properly. Abiomed is implementing hardware updates through its servicing process.

Serious·FDA·Jun 3, 2026

The proximal clasp on Bolton Medical's RelayPro Thoracic Stent-Graft System may disconnect from the outer control tube during use. This disconnection could prevent the stent graft from being released properly from its delivery system. The FDA has issued a labeling update to inform physicians and hospitals of this potential issue.

Serious·FDA·Jun 3, 2026·Bolton Medical

AVEVA nicotine patches (14 mg) distributed by Rugby Laboratories have elevated levels of chemical impurities that exceed safety standards for shelf life. The issue was discovered during stability testing of specific lots. No injuries have been reported.

Moderate·FDA·Jun 3, 2026·AVEVA

Philips is recalling X-ray tube cooling units, type CU3101, that were made between February 2016 and May 2020. The deaeration hose may degrade and leak oil, which can reduce cooling. When oil flow drops too low, the system switches to low-dose fluoroscopy and shows a tube cooler message that restarting does not clear. The recall covers 3 product lines with about 5,000 affected units, and no injuries have been reported.

Moderate·FDA·May 27, 20263 products

C.R. Bard has recalled certain Silastic Brand Foley Catheters (5cc and 30cc models) due to staining on the catheter surface. The affected catheters were distributed across the U.S. and Canada.

Moderate·FDA·May 27, 2026

Certain Philips Azurion fluoroscopy systems may experience mechanical wear in the Float Tabletop control, which could impair the longitudinal and transverse (side-to-side and front-to-back) movement of the examination table. This wear could affect the system's ability to position patients correctly during imaging procedures.

Moderate·FDA·May 27, 2026

Medtronic is recalling nine models of retrograde cannulas used in cardiopulmonary bypass procedures. Certain lots may have a sterile barrier that could be breached, which could compromise the product's sterility. No injuries have been reported.

Moderate·FDA·May 27, 20269 products

The straight inserter tool on certain OneLIF Interbody Cage implants may fail to attach properly to the cage. This could prevent secure engagement during spinal fusion surgery, potentially causing procedural delays or requiring surgeons to choose a different implant.

Moderate·FDA·May 27, 2026·Novapproach Spine

ICU Medical oncology infusion kits with extension sets may develop leaks during chemotherapy administration. If a leak occurs during therapy, patients may receive less medication than intended, and healthcare workers or patients could be exposed to hazardous drugs.

Moderate·FDA·May 27, 2026

Tangent Endoscopy's Single Use Digital Catheter (models TNG4002-IND and TNG-4007-6pk) can develop fractures at the tip of the shaft during use. While the fractured pieces have not completely detached in reported cases, a broken catheter tip could affect device function or potentially cause patient harm.

Moderate·FDA·May 27, 2026·Tangent Endoscopy

Becton Dickinson is recalling 3 Swan-Ganz catheter product lines, with 589,459 affected units in total. The blue proximal injectate lumen hub can leak or break because of manufacturing and material changes, which may lead to infection, medication loss, or blood loss. No injuries have been reported, and the products were distributed across the US and in many other countries.

Moderate·FDA·May 27, 20263 products

Wellnov Supplements is recalling 14 products, including Joint Nourish, FulviLife Complex, Liposomal multivitamin drops, Liposomal Collagen Booster, Liposomal Kids Liquid Multivitamin Drops, and Liposomal D3, B12 and Sleep sprays. The products are made by VitaminAlly LLC in Chandler, Arizona, and were sold nationwide and in Puerto Rico. The FDA says manufacturing practices fell short in ways that could allow bacterial contamination and possible C. botulinum, and no illnesses have been reported.

Moderate·FDA·May 27, 202614 products

Liquid Blenz Corp's Blackseed Bitters in 16 oz and 32 oz bottles may not have been processed properly, which could allow dangerous botulism bacteria to grow. The product also makes health claims not authorized on bitters products. No illnesses have been reported so far.

Moderate·FDA·May 27, 2026·Blackseed Bitters13 products

Wisconsin Pharmacal Company's MG217 Multi-Symptom Treatment Cream (colloidal oatmeal 2%, 6 oz) has been found to contain Staphylococcus aureus bacteria. The contamination was confirmed in lot #1024088 (expiration 11/30/2026). About 690 tubes were distributed nationwide and to the Bahamas.

Serious·FDA·May 27, 2026·Wisconsin Pharmacal

Safecor Health's Nephronex vitamin B-complex, vitamin C, and folic acid oral liquid supplement was found to contain black particles in the liquid. The affected product is supplied in 5 mL oral syringes. The contamination was identified in three specific lots distributed in Ohio.

Moderate·FDA·May 27, 2026