New Hampshire recalls

Sold nationwide. WAP Sensual Enhancement Capsules were sold without FDA approval and contain three undeclared prescription medications: sildenafil, tadalafil, and flibanserin. These are potent drugs that require a doctor's prescription and can cause serious health problems, especially in people taking other medications or with certain medical conditions.

Serious·FDA·Oct 20, 2026·Erotic Enhancers

Sold nationwide. Right Value Drug Stores LLC is recalling compounded testosterone cypionate injection (200 mg/mL) in 5 mL and 30 mL vials due to lack of sterility assurance. The affected vials were distributed nationwide to medical offices. No injuries have been reported.

Moderate·FDA·Oct 19, 2026·Right Value Drug Stores LLC

Sold nationwide. Ashtel Studios Inc. of Ontario, California is recalling 17 fluoride toothpaste products nationwide because they were made in ways that did not meet FDA manufacturing standards. The products are sold under the Barbie, Hot Wheels, Crayola and My Little Pony names, plus the Brush Buddies, evo, ARU and BB brands. No injuries have been reported.

Moderate·FDA·Oct 19, 2026·PRITAM INTERNATIONAL PRIVATE LIMITED17 products

Sold nationwide. Kayem Foods discovered that some of its ready-to-eat meat and poultry products may have been stored at unsafe temperatures in a warehouse cooler. The products were made between late March and early October 2026. No illnesses have been reported so far.

Serious·USDA·Oct 17, 2026·Kayem

Sold nationwide. Philips Smart-hopping 2.0 AP wireless access points may experience unreliable roaming behavior when older Smart-hopping 1.0 wireless clients move between locations. This can cause loss of connection to the central monitoring system, potentially interrupting patient monitoring in healthcare facilities.

Moderate·FDA·Oct 16, 2026·Philips

Sold nationwide. Axonics has recalled certain lots of its PNE Lead Implant Kit because the 10mL luer lock syringes included in the kit may leak, break, or malfunction. This could affect the safe use of the implant procedure. The recall affects approximately 18,294 kits distributed nationwide and internationally.

Moderate·FDA·Oct 16, 2026·Axonics

Sold nationwide. Medtronic Navigation is recalling four products: certain NDI passive spheres and a biopsy needle kit. The reflective material on these items may vary, which could affect a navigation system's ability to detect and track them. No injuries have been reported.

Moderate·FDA·Oct 16, 2026·Medtronic4 products

Sold nationwide. B. Braun Medical Inc is recalling certain SAFSITE Injection Site valves (model RV1000NC, catalog number 415068) because they may leak or allow blood to flow backward into the IV line. This could affect the safety of IV therapy. The recall affects specific lot numbers with expiration dates in September and October 2029.

Moderate·FDA·Oct 16, 2026·B. Braun

Sold nationwide. Think Surgical's Square Driver robotic component did not meet design specifications. This could cause the pin to become stuck or wobble during surgical drilling procedures. No injuries have been reported.

Moderate·FDA·Oct 16, 2026·Think Surgical

Sold nationwide. Abbott has updated the instructions for use for certain Amplatzer Amulet left atrial appendage occluder devices to address a risk of pulmonary artery injury during the procedure. This is a precautionary update affecting multiple model numbers across all lots and serial numbers.

Moderate·FDA·Oct 16, 2026·Abbott

Sold nationwide. The Philips Lumify portable ultrasound system may fail to recognize previously saved transducer settings, forcing re-registration that requires Wi-Fi or cellular access—unavailable in ambulances, aircraft, or remote field settings. Additionally, the USB cable connection between the transducer and tablet/phone may become unstable or disconnect, disrupting scans. These issues could delay diagnosis or treatment.

Serious·FDA·Oct 16, 2026·Philips

Sold nationwide. Pfizer is recalling specific lots of Levoxyl (levothyroxine sodium) 175 mcg tablets because stability testing found the drug potency fell below required specifications. This means some tablets may contain less active medication than labeled. The recall affects 134 bottles with lot number 24W07, expiring 11/30/2026.

Moderate·FDA·Oct 16, 2026·Pfizer2 products

Sold nationwide. Hepalink USA is recalling Heparin Sodium Injection (5,000 USP Units/mL) due to lack of assurance that the product is sterile. The affected multidose vials have lot number CU03232A with an expiration date of January 31, 2028. This product is used in hospitals and medical settings.

Moderate·FDA·Oct 16, 2026·Techdow

Sold nationwide. Certain lots of Telmisartan and Amlodipine 40mg/5mg tablets manufactured by Mylan Pharmaceuticals (Viatris) may contain higher-than-specified amounts of Telmisartan, the blood pressure-lowering active ingredient. The affected lots were distributed nationwide. No injuries have been reported.

Moderate·FDA·Oct 16, 2026·Viatris

Sold nationwide. Ascend Laboratories is recalling one lot of amlodipine and olmesartan medoxomil combination tablets (10mg/40mg) because they do not dissolve properly in the body. This means the medication may not work as intended. The affected lot was distributed nationwide.

Moderate·FDA·Oct 16, 2026·Ascend Laboratories

Sold nationwide. usOpal's Xalirium portable bed rails can trap users between the rail and mattress, or inside the rail frame, creating a serious risk of asphyxiation. The rails also lack required warning labels and do not meet safety standards for stability and retention straps.

Serious·CPSC·Oct 15, 2026·usOpal

Sold nationwide. Primark's 101 Dalmatians faux leather coin purses contain higher levels of phthalates than allowed. Phthalates can be harmful to young children, especially if ingested, and may affect development and hormones.

Serious·CPSC·Oct 15, 2026·Primark

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