Check a product

Macleods Pharma USA is recalling Levothyroxine Sodium Tablets USP 150 mcg because they may contain less active ingredient than labeled. This means the medication may not work as intended to treat thyroid conditions. The affected lot is 16240062A with an expiration date of March 2026.

Moderate·FDA·Apr 1, 2026

Chiesi USA is recalling specific lots of CUROSURF, a medication given to premature infants to help them breathe. The company cannot confirm that all vials are sterile, which means they may be contaminated. No infections have been reported so far.

Moderate·FDA·Apr 1, 2026

Radnostix Gelatin Capsule Packs used with Sodium Iodide I-131 Kit have failed quality specifications. The affected capsules may not perform as intended. Three specific lots distributed nationwide are involved.

Moderate·FDA·Apr 1, 2026·Radnostix

Hologic's Aptima HPV Assay test kits (Master Lot 929785) may produce invalid results or false negatives, meaning they could fail to detect HPV infection. The affected kits were distributed to healthcare facilities in California, Florida, Iowa, Illinois, Missouri, North Carolina, New Mexico, Puerto Rico, and Tennessee.

Moderate·FDA·Mar 25, 2026

Diagnostica Stago's STA Liatest D-Di blood test kits are giving inaccurate measurements for D-dimer (a marker used to help rule out blood clots). The kits are showing higher-than-actual results across all test ranges. These kits are used in hospital and reference laboratories on specific analyzer machines.

Moderate·FDA·Mar 25, 2026

ConvaTec's EsteemBody Drainable Pouch (model REF:423643, 10–45mm) may leak because of a manufacturing issue. The affected pouches have lot numbers 5K00011 or 5K00714 and have been distributed worldwide. No injuries have been reported.

Moderate·FDA·Mar 25, 2026·ConvaTec3 products

LeMaitre Vascular is recalling one unit of Artegraft Vascular Graft (Model AG740) distributed in Illinois due to a labeling mix-up on the outer packaging. The product box was labeled with an incorrect lot number, which could cause confusion during clinical use. No injuries have been reported.

Moderate·FDA·Mar 25, 2026·LeMaitre Vascular

The Welch Allyn Spot Vision Screener VS100 (software version 3.2.0.1) may display an unintended flickering screen due to a software issue. Flickering lights can trigger seizures in people who are photosensitive.

Moderate·FDA·Mar 25, 2026

The external screws that secure the cover on the Howmedica Osteonics MICS3 Angled Sagittal Saw Attachment may loosen during use and detach. This affects all units with part number 210490 distributed across the United States and several other countries. No injuries have been reported.

Moderate·FDA·Mar 25, 2026

GE is recalling three versions of Centricity Universal Viewer software, a program that displays medical images, including mammograms. User login credentials may be exposed on the local workstation, which could let an unauthorized person affect system availability or manipulate data. The recall covers 2,405 affected units, and no injuries have been reported.

Moderate·FDA·Mar 25, 20263 products

Abbott Diagnostics has recalled certain lots of the ID NOW Influenza A & B 2 test kit because they produce an unusually high number of invalid results compared to what the instructions say to expect. Invalid results mean the test does not give a clear positive or negative answer, requiring a retest.

Moderate·FDA·Mar 25, 2026

Winder Laboratories is recalling certain batches of their grape-flavored multivitamin with fluoride chewable tablets because they contain less vitamin D than stated on the label. The FDA discovered this during an inspection. The affected products are the 0.25 mg and 1 mg formulations with specific lot numbers and expiration dates in October and November 2025.

Moderate·FDA·Mar 25, 2026·Winder Laboratories

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

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

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

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

Certain Penner Pacific Bathing Spa models do not have a unique device identifier (UDI) as required by FDA regulations. This affects 206 units with specific serial numbers distributed nationwide. No injuries have been reported.

Moderate·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