Check a product

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

Strides Pharma Children's Ibuprofen Oral Suspension (100 mg per 5 mL) has been recalled because some bottles contain gel-like masses and black particles. The affected bottles are 4 FL OZ (120 mL) size with lot numbers 7261973A or 7261974A, expiring 01/31/2027. No injuries have been reported.

Moderate·FDA·Mar 25, 2026·Strides

White Oak Pastures grassfed ground beef sold at Mom's Organic Markets may contain metal fragments. The product was produced on February 26, 2026, and sold in 16 oz packages with a sell-by date of March 19, 2026. No injuries have been reported, but the USDA is alerting consumers in case any packages remain in freezers.

Moderate·USDA·Mar 23, 2026·White Oak Pastures

Tainoki Fine Furniture is recalling height-adjustable swivel office chairs sold at HomeGoods because the metal base can bend during use, creating a fall risk. The recall affects Noah, Owen, and Warren model chairs sold between August and December 2025. No injuries have been reported.

Moderate·CPSC·Mar 19, 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

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

Physio-Control infant and child defibrillator electrodes may separate or peel apart during use, which could prevent proper delivery of therapy. The affected electrodes are pre-gelled, self-adhesive pads designed for use with automated external defibrillators (AEDs) on children under 8 years old or weighing less than 55 pounds. No injuries have been reported.

Moderate·FDA·Mar 18, 2026·Physio-Control

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

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

CNC Noodle is recalling two noodle products, Steam Noodles and Zhong Hua Chao Mian Noodle, because the labels do not declare wheat. The recall covers about 737 cases of 3 to 10 pound bags, distributed only in California and Nevada. No illnesses have been reported.

Moderate·FDA·Mar 18, 20262 products

Cocos Wholesale is recalling two frozen Coco's Italian Market products: Heat-n-Eat Fettuccini Alfredo and a Cannoli Making Kit. The labels list semolina and durum flour but do not declare wheat, which is a major allergen. The products were distributed in Tennessee, and no injuries have been reported.

Moderate·FDA·Mar 18, 20262 products

Lowes Foods sour cream and onion flavored potato chips (8 oz bags) have incorrect Nutrition Facts labels. The sodium content is listed lower than it actually is, and monosodium glutamate (MSG) is not listed as an ingredient even though it is present in the product. This matters if you avoid high sodium or MSG for health reasons.

Moderate·FDA·Mar 18, 2026

Willamette Valley Pie Company is recalling two sizes of frozen raw blueberry crumble pies, an 8-inch and a 9-inch, because they may be contaminated with Listeria monocytogenes. The pies were distributed in Illinois and Oregon, and no illnesses have been reported.

Moderate·FDA·Mar 18, 20262 products

Hortex Mieszanka 9 spring vegetable mix (15.87 oz packages) may contain glass fragments. The affected product has lot number SoC1070925 and was distributed in Illinois. No injuries have been reported so far.

Moderate·FDA·Mar 18, 2026·Hortex

Palmetto Gourmet Foods' Vegetarian Chicken Flavor Ramen Express contains Yellow #5 food coloring that is not listed on the package label. This undeclared ingredient can cause allergic reactions in people sensitive to Yellow #5. The recall affects packages with a Best By Date before January 15, 2027, distributed across 31 states.

Moderate·FDA·Mar 18, 20262 products

Some frozen La Boulangerie Turkey Pesto & Swiss Cheese Pockets sold at Costco in the Midwest contain ham and cheese instead of the labeled turkey filling. The mislabeling was discovered after two customer complaints. No one has reported getting sick.

Moderate·USDA·Mar 13, 2026·La Boulangerie