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Apotex Corp. is recalling specific lots of brimonidine tartrate/timolol maleate eye drops because the manufacturer cannot confirm the product was sterilized properly. The affected lots are VJ8599 (expires 09/30/2026) and VL1668 (expires 01/31/2027). No infections or injuries have been reported so far.

Moderate·FDA·Mar 25, 2026

Somerset Therapeutics is recalling one lot of dexamethasone sodium phosphate injection because testing found impurity levels above acceptable limits as the product approached its expiration date. The affected lot (A240421, expiring 07/31/2026) was distributed nationwide. No injuries have been reported.

Moderate·FDA·Mar 25, 2026·Somerset Therapeutics

A 1 mg Pitavastatin tablet was found mixed into a bottle labeled as containing 2 mg tablets. This occurred in one lot (A252487) distributed in Tennessee. Taking the wrong dose by mistake could affect how well your cholesterol medication works.

Moderate·FDA·Mar 25, 2026·Annora Pharma

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

Medline is recalling 2 product groups of surgical gowns and drapes, about 127,572 units in total. The fabric may separate in layers (delaminate) early when washed using the included laundering instructions. If a separated product is used during surgery and fluid passes through, there may be a risk of infection.

Moderate·FDA·Mar 18, 20262 products

Medline and Cardinal Health have recalled specific lots of chest drainage kits used in cardiac surgery because the instructions needed to clarify that these devices are intended only for adult patients age 18 and older. The kits were distributed nationwide in California and internationally to Chile and Panama.

Moderate·FDA·Mar 18, 2026

Altruan is recalling three Strep A test products, including the Wondfo Streptococcal A At-Home Self-Test, Clearest Strep-A Cassette Test, and Bisaf Strep A Self-Test. The tests were distributed nationwide and the FDA has not cleared them. No injuries have been reported.

Moderate·FDA·Mar 18, 2026·Altruan3 products

The Lutronic CLARITY II Laser System (Model 1110200210) may spark or pop during use, potentially causing burns to patients. The FDA has identified over 1,500 affected units based on serial number.

Moderate·FDA·Mar 18, 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 three Artelon FlexBand augmentation devices because they failed bacterial endotoxin testing. The recall covers three product listings and was distributed across the US and in several other countries. No injuries have been reported.

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

Beckman Coulter is recalling two clinical chemistry analyzer models, the DxC 700 AU and the AU5800, because the calibration monitor PC can show database errors if it is left open for more than 15 minutes. When this happens, the system can stop analyzing samples, which may delay test results, diagnosis, or patient treatment. No injuries have been reported.

Moderate·FDA·Mar 18, 20262 products

Boston Scientific is recalling certain EndoVive Safety PEG Kits that contain ChloraPrep Triple Swabsticks with open or damaged packaging. The affected swabsticks may have lost sterility or dried out. The rest of the kit components remain safe and unaffected.

Moderate·FDA·Mar 18, 2026

Medartis AG recalled specific lots of APTUS 2.5 TriLock Screws used in hand, forearm, shoulder, and foot surgery because some packages may contain 2.8mm screws instead of the labeled 2.5mm size. Using the wrong size screw could affect surgical fixation.

Moderate·FDA·Mar 18, 2026·Medartis2 products

Trividia Health is recalling the owner's booklets and instructions for use for four groups of TRUE METRIX blood glucose meters and kits. The labeling does not clearly explain that the E-5 error code can mean a very high blood glucose level or tell users to contact a healthcare professional right away. No injuries have been reported.

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

Instrumentation Laboratory is recalling 20 GEM PAK cartridges for the GEM Premier 5000 system. Customers reported that the cartridges may show 'Process Control Solution Not Detected' (PCSND) errors during warm-up, sometimes repeatedly, which ejects the cartridge and requires inserting a new one. No injuries have been reported.

Moderate·FDA·Mar 18, 202620 products

Waldemar Link is recalling 13 Endo-Model implant components, including replacement plateaus and connection components with PE-Plateau. The bushing on these implants could detach from the screw shaft because of a longitudinal fracture. No injuries have been reported.

Moderate·FDA·Mar 18, 202613 products

Exactech is recalling two surgical instrument products, the Equinoxe Ergo Modular Impactor Handle and the Equinoxe Core Instrument Kit, because the impactor handle may be missing a cross-pin. The recall includes 120 handles and 596 kits, distributed in the US and several other countries. No injuries have been reported.

Moderate·FDA·Mar 18, 2026·Exactech2 products

Penner Patient Care is recalling 10 product groups of its Pacific Bathing Spa, covering about 1,300 units nationwide. The devices do not have a unique device identifier (UDI) label as required. No injuries have been reported.

FDA·Mar 18, 2026·Penner Patient Care10 products

Raz Design mobile shower commode chairs may have improperly engaged rear seat brackets due to a vendor modification. This could cause the seat to become loose or detach during use. The recall affects multiple Raz models nationwide.

Moderate·FDA·Mar 18, 2026·Raz Design

A safety feature in the IBA PROTEUS 235 proton therapy system can become disabled, preventing automatic beam shutdown if an external gating device loses signal. This affects only 4 specific units worldwide and may result in incorrect radiation delivery during treatment.

Moderate·FDA·Mar 18, 2026·Ion Beam Applications

Becton Dickinson discovered that some Luer Slip syringes were accidentally mixed into batches of 10mL Luer-Lok syringes during packaging. This affects product Catalog Number 301029, Lot 5268614, distributed in California and Texas. No injuries have been reported.

Moderate·FDA·Mar 18, 2026

Medline's Unna-Z Stretch Zinc Paste Bandage has incomplete ingredient information on the label. The product contains castor oil and calamine, but these ingredients were not listed on the packaging. This labeling error affects batches distributed in Illinois.

Moderate·FDA·Mar 18, 2026·KOB

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

Failed Tablet/Capsule specifications: Red dots inside capsule and melted capsule caused by oxidized Icosapent ethyl, the active ingredient.

FDA·Mar 18, 2026

Advanced Bionics is recalling certain Sky CI M90 Sound Processors because the label on the package does not match the product inside. Two units with specific serial numbers (249596 and 249603) are affected. No injuries have been reported.

Moderate·FDA·Mar 11, 2026·Advanced Bionics

Vascutek vascular repair grafts (Gelsoft Plus and Gelweave models) were labeled with expiration dates that are too long. The shelf life was incorrectly calculated from the packaging date instead of the gel treatment date. This means some devices may expire sooner than the label states.

Moderate·FDA·Mar 11, 2026·Vascutek

Diagnostica Stago's STA Liatest Free Protein S testing kits (model REF 00516) may produce inaccurate results, potentially underestimating free protein S levels in normal patient samples. This affects specific lot numbers distributed nationwide and internationally. No injuries have been reported.

Moderate·FDA·Mar 11, 2026

Esaote has identified a weakness in the probe body on a specific production batch that may cause liquid to leak from the cable connection area. Five units with specific serial numbers were distributed in North Carolina and Texas.

Moderate·FDA·Mar 11, 2026·Esaote

Olympus is recalling two single-use biopsy valves, models MAJ-210 and MAJ-1218, which attach to the instrument channel port of compatible endoscopes. The valves may release rubber fragments during use. No injuries have been reported.

Moderate·FDA·Mar 11, 20262 products

Datascope Corp. identified that the battery runtime and cycle specifications in the instruction manual for the CS100 IABP (intra-aortic balloon pump) device are incorrect and need to be updated. The device itself is not defective, but users may rely on outdated battery information.

Moderate·FDA·Mar 11, 20262 products