New Hampshire recalls
1,930 federal recalls affecting New Hampshire in the last 12 months: 57 sold in New Hampshire plus 1,873 sold nationwide. From the CPSC, FDA, USDA and NHTSA.
Recent recalls
Page 8 of 65- Philips Spectral CT recalled for software image and motion issues
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.
ModerateFDAOct 14, 2026Philips
- HALYARD laparoscopy packs recalled for undeclared latex catheter
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.
ModerateFDAOct 14, 2026GRI Medical & Electronic Technology
- QUANTUM OPS Beach Chair positioner recalled for weld defect
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.
ModerateFDAOct 14, 2026Quantum Ops
- Steris VERIFY biological indicators recalled for spore shelf-life issue
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.
ModerateFDAOct 14, 2026Steris6 products
- Sweet Sensi THC gum drops recalled for Staphylococcus aureus
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.
ModerateFDAOct 14, 2026Sweet Sensi
- X10 and biQ-FEL supplements recalled for undeclared sildenafil and tadalafil
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.
SeriousFDAOct 14, 2026A&P Creations2 products
- bettergoods Lemon Alfredo Fettuccine recalled for Listeria risk
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.
SeriousFDAOct 14, 2026bettergoods
- Berlin Seeds alfalfa seeds recalled for possible E. coli/Salmonella
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.
SeriousFDAOct 14, 2026Berlin Seeds
- Donutful chocolate dipped cake donuts recalled for undeclared milk
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.
SeriousFDAOct 14, 2026Donutful
- LEASA alfalfa sprouts recalled for E. coli risk
LEASA is recalling two sizes of alfalfa sprouts sold in plastic clamshell containers: Living Alfalfa Sprouts (4 oz.) and Alfalfa Sprouts (6 oz.). The seeds used to grow the sprouts may be contaminated with E. coli. The products were distributed in Florida and New Hampshire, and no illnesses have been reported.
SeriousFDAOct 14, 2026LEASA2 products
- Orbi 20 and Omni Gold creams recalled for mercury contamination
Sold nationwide. DANALVIG LLC is recalling two skin whitening creams, Orbi 20 Whitening Cream and Omni Gold Anti-Marks Cream Extra Brightening, sold nationwide through eBay. FDA analysis found the products contain mercury, and both are made by White Gold International in Lahore, Pakistan. No injuries have been reported.
SeriousFDAOct 14, 2026DANALVIG LLC2 products
- Apothecary Pharma tirzepatide and NAD+ injections recalled over sterility
Sold nationwide. 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.
ModerateFDAOct 14, 2026Apothecary Pharma2 products
- Taro and Northstar Rx tretinoin cream recalled for impurities
Sold nationwide. 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.
ModerateFDAOct 14, 2026Sun Pharmaceutical3 products
- Carolina Infusion compounded injectables recalled for sterility risk
Sold nationwide. 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.
ModerateFDAOct 14, 2026Carolina Infusion16 products
- Cipla USA fosfomycin granules recalled for failed impurity specifications
Sold nationwide. 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.
ModerateFDAOct 14, 2026Cipla
- Preferred Pharmaceuticals Lidocaine Ointment recalled for content uniformity failure
Sold nationwide. 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.
ModerateFDAOct 14, 2026Preferred Pharmaceuticals
- Best Choice, LEADER eye drops and more recalled for sterility
Sold nationwide. K.C. Pharmaceuticals is recalling eight sterile eye drop products sold nationwide because they may not be sterile. The products are sold under the Best Choice, Equaline, Good Sense, LEADER, exchange select and Crocodile Tears names. No injuries have been reported.
SeriousFDAOct 14, 2026K.C. Pharmaceuticals8 products
- Centric Compounding vitamin injections recalled for contamination
Sold nationwide. Centric Compounding of Houston, Texas, is recalling three sterile vitamin products sold as Tri-Immune Boost, Glutathione 200 mg/mL and Multidose Myers Cocktail vials. Test results found bacterial endotoxin levels outside acceptable limits. No injuries have been reported.
SeriousFDAOct 14, 2026Centric Compounding4 products
Para Bien Al Grano recalled for undeclared sesameSold nationwide. Pan Pepin Inc. is recalling certain lots of Para Bien Al Grano cereal because it contains sesame that is not listed on the label. People with a sesame allergy or sensitivity could have a serious or life-threatening allergic reaction if they eat this product. The product was sold in Puerto Rico.
SeriousFDAOct 13, 2026Para Bien
Par Pharmaceutical Brevital Sodium recalled for particulate matterSold nationwide. Par Pharmaceutical is recalling two lots of Brevital Sodium 500 mg/vial, an injectable anesthetic used in hospitals, because they contain tiny cellulose particles. These particles could potentially cause serious blood vessel blockages or clotting if injected. No adverse events have been reported so far.
SeriousFDAOct 8, 2026Par Health
Gardeners Basics broccoli sprouting seeds recalled for Salmonella riskSold nationwide. Gardeners Basics broccoli sprouting seeds may be contaminated with Salmonella, a bacteria that can cause serious illness. The contamination was identified in the seed supplier's bulk lot, which was also linked to a multistate foodborne illness outbreak. No illnesses have been reported so far.
SeriousFDAOct 8, 2026Gardeners Basics
- PHP Animal Health pet eye drops recalled for sterility assurance
Sold nationwide. PHP Animal Health Pet Drops lubricant eye drops may not be sterile due to a manufacturing issue. The affected products are single 15 mL bottles and twin packs distributed nationwide. No injuries have been reported.
ModerateFDAOct 8, 2026PHP Animal Health
The Conqueror Avengers medals recalled for magnet ingestion riskSold nationwide. The Avengers Infinity Gauntlet medals sold through The Conqueror App contain high-powered magnets that can detach and be swallowed by children. Swallowed magnets can attract each other or metal objects, causing intestinal perforations, blockages, and serious internal injuries.
SeriousCPSCOct 8, 2026The Conqueror
Snow Peak propane inserts, lava rocks recalled for fire riskSold nationwide. Snow Peak's Takibi propane inserts and lava rocks can cause the rocks to ignite and explode when heated, creating a serious burn and fire hazard. The company has received one report of lava rocks exploding with minor property damage.
SeriousCPSCOct 8, 2026Snow Peak
Romorgniz six-drawer dressers recalled for tip-over and entrapment riskSold nationwide. Romorgniz six-drawer wooden dressers can tip over and trap children if not anchored to the wall. These dressers do not meet federal safety standards for furniture stability. About 12,078 units were sold online through Amazon between May 2025 and August 2026.
SeriousCPSCOct 8, 2026Jinhao Sen
Pacearth swing seats recalled for fall injury riskSold nationwide. The metal carabiners, quick links, or webbing straps on Pacearth U-type swing seats can break during use, causing the seat to fall. The company has received at least 30 reports of falls, including nine injuries such as fractures and head trauma.
SeriousCPSCOct 8, 2026Pacearth Direct
ONTHEWEI baby bath seats recalled for drowning riskSold nationwide. ONTHEWEI baby bath seats can tip over during use because they are unstable, creating a risk of drowning. The seats violate the federal safety standard for infant bath seats. About 2,140 units were sold online through Amazon between April and January 2026.
SeriousCPSCOct 8, 2026OnTheWei
Van Rysel GRVL AF bicycles recalled for crash riskSold nationwide. The front lock nut on these gravel bicycles can loosen during use, which may cause the front wheel to dislodge or become unstable. This poses a serious crash hazard to riders. The issue affects specific Van Rysel GRVL AF models sold at REI Co-op between March 2025 and August 2026.
SeriousCPSCOct 8, 2026Decathlon
DR Power trimmer mowers recalled for fire and burn riskSold nationwide. Grass and debris can accumulate inside DR Power Pilot and Premier trimmer mowers and ignite, creating a fire hazard. The company has received 19 reports of fires, including two minor burn injuries.
SeriousCPSCOct 8, 2026Generac
Giant SureLock LED bike keys recalled for battery ingestion riskSold nationwide. LED-light keys included with certain Giant SureLock bicycle lock sets contain button batteries that children can access and swallow. Swallowing these batteries can cause serious internal injuries, chemical burns, and death. The recalled keys were sold from March 2023 through August 2026.
SeriousCPSCOct 8, 2026Giant