Arizona recalls

Sold nationwide. Holsum Spinach Flour Tortillas (large, 8-count packages) contain FD&C Blue No. 1 and FD&C Yellow No. 5 food dyes that are not listed on the label. People with sensitivities or allergies to these dyes may be affected. The affected product was distributed in Puerto Rico and the US Virgin Islands.

Moderate·FDA·Oct 21, 2026·Holsum

Sold nationwide. Par Health USA's Dexmedetomidine HCl injection vials contain unwanted particulate matter, identified as cellulose or stopper material. The contamination affects two specific lots distributed nationwide. This is a prescription medication used during anesthesia and sedation.

Serious·FDA·Oct 21, 2026·Paragon 28

Sold nationwide. American Health Packaging distributed metoclopramide 5 mg tablets that contained foreign tablets or capsules mixed in with the correct medication. The contamination was found in two lot numbers distributed nationwide. No injuries have been reported.

Moderate·FDA·Oct 21, 2026·American Health Packaging

Sold nationwide. Houston Rx is recalling two injectable products, a tirzepatide/niacinamide 2 mL vial and a sermorelin 10 mL vial, because the company cannot assure they are sterile. The recall covers 71 vials distributed nationwide in the USA, and the FDA has reported no injuries.

Moderate·FDA·Oct 21, 2026·Houston Rx2 products

Sold nationwide. Zydus Pharmaceuticals is recalling specific lots of Hydrocortisone Sodium Succinate for Injection because the drug failed quality testing for impurities and degradation. The affected lots (LB00047A and LB00048A, expiring 03/2028) were distributed nationwide. No injuries have been reported.

Moderate·FDA·Oct 21, 2026·Zydus

Sold nationwide. Teva Pharmaceuticals discovered that some bottles of Metoclopramide 5 mg tablets contain foreign tablets or capsules mixed in with the correct medication. The contamination was found in specific lots distributed nationwide. No injuries have been reported.

Moderate·FDA·Oct 21, 2026·Teva

Sold nationwide. Ventec Life Systems is recalling 12 ventilator models used for ventilatory support, including VOCSN+Pro, VC+Pro, VOCSN, VCSN+Pro, V+Pro, VC, V+ Pro Emergency and V*Home, some in Japan versions. The internal flow transducer cable connector may disconnect from the internal board, which could cause the system to reboot and interrupt ventilation therapy. The notice reports no injuries, and the devices were distributed nationwide, including Puerto Rico.

Serious·FDA·Oct 20, 2026·Ventec Life Systems12 products

Sold nationwide. Cronus Pharma is recalling one lot of AnaSed Equine Injection (xylazine 100 mg/mL), a sedative for horses, due to reports of product discoloration. The affected lot is C25110AV1 with an expiration date of November 2027. Discoloration may indicate a quality issue with the medication.

Moderate·FDA·Oct 20, 2026·AnaSed

Great Value Fruit Cocktail in Fruit Juice from Concentrate (15 oz cans) has been recalled due to potential contamination with elevated levels of lead. The affected product was distributed to Walmart stores in Alabama, Arizona, Louisiana, New Mexico, Pennsylvania, Washington, and Wyoming. The specific lot number is 6FCB 04 C2263 with a "Best If Used By" date of September 1, 2027.

Serious·FDA·Oct 20, 2026·Great Value

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

Sempio Food Services, Inc. is recalling Yellow Peach canned peaches (14.10 oz cans, UPC 8801005320825, lot code 2026 06 01) because they contain elevated levels of lead. The product was distributed to Asian grocery stores across multiple states. No injuries have been reported.

Moderate·FDA·Oct 19, 2026·Sempio

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