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Bolts that secure the longitudinal movement mechanism on the Canon Medical Alphenix INFX-8000C/B5 imaging system may loosen over time. This can cause the patient tabletop to shift unexpectedly, leading to misalignment during imaging procedures and motion errors.

Moderate·FDA·Oct 14, 2026

Certain Polymedco SEDIPLAST blood collection tubes (models S-100 and S-1000) may have a defect that causes increased resistance when a pipette is inserted. This pressure buildup can cause the tube cap to detach or be forcibly ejected, potentially exposing lab workers and work areas to blood.

Moderate·FDA·Oct 14, 2026·Polymedco

AVID Medical is recalling 15 surgical kits and packs, including DaVinci and Shands Jacks products, because they may be contaminated with a lubricant used during manufacturing. The recalled kits were distributed nationwide, with the listed states including AZ, CA, FL, MD, NE, and TX. No injuries have been reported.

Moderate·FDA·Oct 14, 202615 products

One personalized pelvic implant was shipped to the wrong customer due to a distribution error. The device is designed specifically for individual patients and should not be used by anyone other than the intended recipient.

Moderate·FDA·Oct 14, 2026·Onkos Surgical2 products

Stryker Sustainability Solutions is recalling a specific lot of BARD EP XT Decapolar Steerable diagnostic catheters (Reference 201007) used in heart rhythm procedures. Some units may have a compromised sterile barrier on the primary pouch packaging, which could allow contamination if the catheter is used. This poses a risk of particle buildup, infection, or blood clots.

Moderate·FDA·Oct 14, 2026

Beckman Coulter identified a software issue in its DxC 500i and DxC 500 AU Clinical Chemistry Analyzers used for testing plasma samples. After a user changes a test to non-default units and later activates a configuration change, the analyzer may revert to the default units without warning, which can lead to falsely elevated reported results. The recall covers 2 product groups with 6 modules and analyzers in total.

Moderate·FDA·Oct 14, 20262 products

DRG International's Sperm Ab ELISA test (model EIA-1826) may return false negative results, meaning it could fail to detect sperm antibodies when they are actually present. This affects lot 320K046 distributed worldwide, including the US and multiple countries in Europe and Asia.

Moderate·FDA·Oct 14, 2026·DRG

Safeguard US compression bandages used in trauma kits and first aid bags may degrade over time, potentially allowing foreign material to enter a wound. This degradation could require additional wound cleaning and may increase the risk of infection or scar tissue formation.

Moderate·FDA·Oct 14, 2026·Safeguard

Limitless Cryo Spa LLC distributed Glypto cryo machines without obtaining required FDA 510(k) clearance. The devices were supplied to facilities nationwide. No injuries have been reported.

Moderate·FDA·Oct 14, 2026·Limitless Cryo Spa

Cardinal Health Presource Packs contain Medtronic Microstream components that may be difficult to disconnect from a patient's breathing tube. Medtronic has updated the instructions for these kits to address this issue. The difficulty could delay treatment or cause unintended removal of the tube, potentially leading to serious breathing complications.

Moderate·FDA·Oct 14, 2026

Philips Medical Systems has recalled certain Spectral CT and Spectral CT 7500 RT imaging systems due to software problems. These issues may cause image artifacts, incorrect slice thickness, or unintended movement of the system during operation.

Moderate·FDA·Oct 14, 2026

HALYARD Laparoscopy Comprehensive Pack II (REF: 49332) was labeled as "latex free" but contained a latex urethral catheter. This mislabeling poses a risk to patients with latex allergies who may use the kit. The recall affects 396 kits with specific lot numbers distributed nationwide.

Moderate·FDA·Oct 14, 2026·GRI Medical & Electronic Technology

QUANTUM OPS ADAPTABLE Beach Chair surgical positioners contain an inadequate weld in the patient head positioning system (BC-0105 subcomponent). This manufacturing defect could potentially affect the stability and safety of the device during surgical procedures. The defect was identified in specific lot numbers distributed in California and Texas.

Moderate·FDA·Oct 14, 2026·Quantum Ops

Steris is recalling six VERIFY biological indicator and challenge pack products used to monitor steam sterilization cycles. The spore population in these products may fall below its minimum shelf-life specification, so an indicator could show no growth even when a steam cycle did not achieve the intended spore reduction. No injuries have been reported.

Moderate·FDA·Oct 14, 20266 products

J K Patisserie & Bakery is recalling 3 baked goods sold in cardboard boxes in New York and New Jersey: Lemon Blueberry Loaf, Chocolate Chip Cookies, and Croissants. The ingredient lists include soybean oil and soy lecithin, but soy is not listed in the allergen statement, so people with soy allergies could be at risk without knowing it. No injuries have been reported.

Moderate·FDA·Oct 14, 20263 products

Saint Francis Apizza is recalling four 17 oz. frozen pizzas sold in Kentucky and Ohio because they contain soybean oil and soy lecithin that are not listed on the label. People with soy allergies could react if they eat them. No illnesses or injuries have been reported.

Moderate·FDA·Oct 14, 20264 products

Sweet Sensi Elevated Edibles Hybrid Gum Drops in Passion Guava Kush flavor (Batch #1811) have been found to contain Staphylococcus aureus bacteria. The affected products are sold in 10-count and 30-count pouches nationwide.

Moderate·FDA·Oct 14, 2026·Sweet Sensi

Queso Palmita Pastel de Queso (Cheese Pie) contains milk that is not declared on the label. The product was distributed in Texas. People with milk allergies or sensitivities who consume this product could have a serious allergic reaction.

Moderate·FDA·Oct 14, 2026

FreshPoint Central Florida's Cranberry Chicken Salad Wedge contains egg, but the allergen warning label does not clearly state this. Egg is listed in the ingredients, but consumers checking the "Contains" statement on the package may not see the allergen warning and could have a serious allergic reaction.

Moderate·FDA·Oct 14, 2026

PepsiCo is recalling specific 28 oz. bottles of Gatorade Lemon Lime, Lemon Lime Zero, Orange, and Orange Zero because they contain Yellow No. 5 and/or Yellow No. 6 food dyes that are not listed on the label. This is a concern for people with allergies or sensitivities to these dyes, or those who avoid them for dietary reasons.

Moderate·FDA·Oct 14, 2026

WinCo Foods Salsa Bean Dip Express Trays (54 oz) and Salsa Bean Dip Catering Trays (16 inch) contain recalled peppers that were contaminated due to a pest issue. The affected products were sold refrigerated with a 4-day shelf life and distributed in eight Western states between mid-August and late September 2026.

Moderate·FDA·Oct 14, 2026

G.L. Mezzetta Inc. is recalling 32 fl oz bottles of Golden Greek Peperoncini (Medium Heat) because they may contain mouse contamination. The affected product was distributed across multiple U.S. states.

Moderate·FDA·Oct 14, 2026·Mezzetta

Apothecary Pharma is recalling two sterile injection vials because the company cannot assure they are sterile. The recall covers 22 vials of Tirzepatide Injection 18 mg/mL (4 mL multi-dose vial) and 1 vial of Apothecary NAD+ Injection 200 mg/mL (6 mL multi-dose vial), distributed nationwide. No injuries have been reported.

Moderate·FDA·Oct 14, 2026·Apothecary Pharma2 products

Sun Pharmaceutical is recalling three tretinoin cream USP 0.05% products, sold in 45 g and 20 g tubes under the Taro and Northstar Rx names. The cream failed the FDA's impurity and degradation standards. No injuries have been reported.

Moderate·FDA·Oct 14, 20263 products

Carolina Infusion LLC of Ridgeland, SC, is recalling 16 compounded injectable products sold as tirzepatide, semaglutide, semaglutide/cyanocobalamin, tirzepatide/cyanocobalamin, sermorelin, Quad-Mix, and Tri-MIX. The company cannot assure that the products are sterile, which relates to the bacteriostatic water used in the formulation and the processing equipment. No injuries have been reported.

Moderate·FDA·Oct 14, 2026·Carolina Infusion16 products

A single lot of IMAAVY (nipocalimab-aahu) injection contains particulate matter that should not be present in the medication. This affects 49 vials distributed in Ohio. The contamination was detected before the medication reached patients.

Moderate·FDA·Oct 14, 2026·Johnson & Johnson

Cipla USA is recalling one lot of Fosfomycin Tromethamine Granules for Oral Solution due to failed quality testing for impurities and degradation. The affected lot (5KA0405, expiring 12/31/2026) was distributed nationwide. No injuries have been reported.

Moderate·FDA·Oct 14, 2026

Preferred Pharmaceuticals' Lidocaine Ointment USP 5% (generic Xylocaine) in 50 g jars failed to meet content uniformity specifications, meaning the active ingredient may not be evenly distributed throughout the product. This affects four specific lots with expiration dates of April 30, 2027. No injuries have been reported.

Moderate·FDA·Oct 14, 2026

BioSpectra, Inc. is recalling one lot of Tris/Tromethamine, USP, GMP, API Grade manufactured at its Bangor, Pennsylvania facility. The affected lot failed stability testing specifications required for pharmaceutical-grade active ingredients.

Moderate·FDA·Oct 14, 2026·BioSpectra

K.C. Pharmaceuticals is recalling multiple brands of sterile eye drops (including Equaline, Good Sense, H.E.B, Quality Choice, and TopCare) because the manufacturer cannot confirm the products were properly sterilized. Eye drops must be sterile to be safe for use in the eyes.

Moderate·FDA·Oct 14, 20268 products