Alabama recalls

1,960 federal recalls affecting Alabama in the last 12 months: 87 sold in Alabama plus 1,873 sold nationwide. From the CPSC, FDA, USDA and NHTSA.

Recent recalls

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  • 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

  • Gatorade 28 oz. drinks recalled for undeclared Yellow dyes

    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.

    ModerateFDAOct 14, 2026Gatorade

  • 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 sesame

    Sold 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 matter

    Sold 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 risk

    Sold 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 risk

    Sold 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 risk

    Sold 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 risk

    Sold 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 risk

    Sold 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 risk

    Sold 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 risk

    Sold 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 risk

    Sold 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 risk

    Sold 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

  • Eden Brothers Calabrese broccoli seeds recalled for possible Salmonella

    Sold nationwide. Eden Brothers LLC is recalling Calabrese Broccoli Seeds in multiple sizes (packets, 1-ounce, and 1-pound) because they may be contaminated with Salmonella. The affected seeds were sold online through EdenBrothers.com and Amazon.com from July through September 2026. No illnesses have been reported so far.

    SeriousFDAOct 7, 2026Eden Brothers

  • Siemens Atellica CH CRP test recalled for falsely elevated results

    Sold nationwide. Siemens has recalled its Atellica CH Revised C-Reactive Protein (RCRP) test kit worldwide due to the potential for falsely elevated results. This diagnostic test is used in clinical laboratories to measure inflammation levels. Laboratories using affected lots may have received inaccurate test results.

    ModerateFDAOct 7, 2026Siemens

  • Wright Medical CHARLOTTE CLAW Screws recalled for manufacturing defect

    Sold nationwide. Wright Medical manufactured CHARLOTTE CLAW Screws (REF: 40122716) with missing threads on the screwheads. These screws are designed to work with the CLAW II Polyaxial Compression Plating System for foot surgery. If used, the missing threads could prevent the screw from securing properly to the plate, potentially requiring surgery to be extended or alternative procedures performed.

    ModerateFDAOct 7, 2026Wright Medical

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