North Carolina recalls

Sold nationwide. Papablic convertible bedside sleepers (model PAPA03001AI) can develop serious safety problems: the mattress can shift and trap a baby between the pad and bottom, creating a suffocation hazard, and the latching mechanism can fail, causing the product to collapse. These defects violate federal safety standards for play yards.

Serious·CPSC·Oct 15, 2026·Papablic

Sold nationwide. Hatsan Blitz and Blitz 777 air rifles can fire unexpectedly when the bolt is released before the rifle is fully cocked. This poses a risk of serious injury or death. One accidental misfire has been reported, but no injuries so far.

Serious·CPSC·Oct 15, 2026·Hatsan

Sold nationwide. The Scotch thermal laminator model TL1302Z can overheat and catch fire. 3M has received 63 reports of the machines smoking, melting, or overheating, including 5 fires. No injuries have been reported so far.

Serious·CPSC·Oct 15, 2026·3M

Sold nationwide. These decorative drinking cups contain crystal stone chips between two layers of glass. The inner glass can break while the cup is in use, creating a risk of cuts or swallowing broken glass. One incident of breakage has been reported, though no injuries have occurred so far.

Serious·CPSC·Oct 15, 2026·Loving Thyself Rocks

Sold nationwide. Intellijoint Surgical's orthopedic navigation workstations may contain a 15-inch MacBook Pro battery that is subject to an Apple recall. The battery may overheat and pose a fire safety risk during use in surgical settings.

Moderate·FDA·Oct 14, 2026·Intellijoint Surgical

Sold nationwide. A software issue in Steris HexaVue Focus Integration System (version 2.0.18) can cause incorrect patient information to appear on manually printed surgical images. This mismatch could lead to documentation errors or clinical images being linked to the wrong patient record.

Moderate·FDA·Oct 14, 2026·Steris

Sold nationwide. LeMaitre Vascular's TufTex Over-the-Wire Embolectomy Catheter (Catalog Number E1651-88, Lot XOT00002181) failed internal testing. The balloon components can fail when exposed to pull force during use, which could compromise the device's ability to remove blood clots safely.

Moderate·FDA·Oct 14, 2026·LeMaitre Vascular

Sold nationwide. Mindray is recalling 8 patient and telemetry monitor product lines because some operator's manuals may be insufficient or unclear about certain physiological alarm functions. The FDA classified this as a Class III recall, and no injuries have been reported. About 275,000 units are affected across the included models.

Moderate·FDA·Oct 14, 2026·Mindray8 products

Sold nationwide. 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·Canon

Sold nationwide. 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

Sold nationwide. 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, 2026·AVID Medical15 products

Sold nationwide. 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

Sold nationwide. Nihon Kohden's CNS-6200 Series Central Nurse Station has a cybersecurity flaw that could allow someone to disrupt the system. If exploited, the flaw could prevent nurses from seeing patient monitoring data and alarms across multiple beds in a hospital.

Serious·FDA·Oct 14, 2026·Nihon Kohden

Sold nationwide. Some MiniMed Flex insulin pumps were shipped without completing required quality verification tests. These pumps may have problems including failure to work at startup, moisture damage, slow charging, connection issues with glucose monitors or the app, missed occlusion alerts, weak alarm sounds, or inaccurate insulin delivery.

Serious·FDA·Oct 14, 2026·Medtronic

Sold nationwide. Medline is recalling two bariatric basic steel rollator walkers, 2,659 units in total. The front wheel assembly can disconnect from the frame, causing the front wheels to become loose or detach during use, which could lead to falls and serious injuries such as head trauma or fractures. No injuries have been reported, and the products were distributed nationwide in the US and to Canada.

Serious·FDA·Oct 14, 2026·Medline2 products

Sold nationwide. 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·Stryker

Sold nationwide. 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, 2026·Beckman Coulter2 products

Sold nationwide. 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

Sold nationwide. 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

Sold nationwide. 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

Sold nationwide. 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·Cardinal Health

Sold nationwide. 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·Philips

Sold nationwide. 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

Sold nationwide. 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

Sold nationwide. 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, 2026·Steris6 products

Sold nationwide. 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

Sold nationwide. A&P Creations is recalling two products that contain sildenafil and tadalafil, prescription ingredients not listed on the label. The products are X10 Natural Enhancement Supplement, distributed by Natur Fuel, and biQ-FEL, distributed by Biofel. About 1,283 retail units of X10 and 3,116 bottles of biQ-FEL were distributed nationwide. No injuries have been reported.

Serious·FDA·Oct 14, 2026·A&P Creations2 products

Sold nationwide. bettergoods Lemon Alfredo Fettuccine pasta, distributed by Walmart, has been recalled because it may be contaminated with Listeria monocytogenes, a bacterium that can cause serious infection. The affected product is packed in a yellow sealed bag with a best-by date of September 21, 2027.

Serious·FDA·Oct 14, 2026·bettergoods

Sold nationwide. Berlin Seeds alfalfa sprouting seeds may be contaminated with E. coli or Salmonella due to a supplier issue. The affected product was sold in multiple bag sizes (1/4 lb. to 50 lb.) through the company's retail store in Millersburg, Ohio, and online.

Serious·FDA·Oct 14, 2026·Berlin Seeds

Sold nationwide. The Better Bakehouse Snack Company's Donutful Chocolate Dipped Vanilla Cake Donuts contain milk that is not listed on the package label. This poses a risk to people with milk allergies or lactose intolerance. The affected product is lot #26078 with a best-by date of 09/15/2026, distributed nationwide.

Serious·FDA·Oct 14, 2026·Donutful