Arizona recalls
3,557 federal recalls affecting Arizona in the last 12 months - 194 Arizona-specific plus 3,363 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-03-04FDA-DeviceMedlineClass IINationwideStop using Medline Sterile Saline Wound Wash
Medline Industries recalled its 7.1 FL OZ Sterile Saline Wound Wash because the manufacturer may not have properly sterilized the product to meet safety standards. This affects all lots of model MDSALINE7 distributed nationwide and in the Caribbean. No injuries have been reported.
- 2026-03-04FDA-FoodPrime Food Processing LLC.Class IStop using Prime Food Processing dried croaker fish
Prime Food Processing dried croaker fish (8 oz packages) may contain uneviscerated fish—meaning the internal organs were not removed before drying. Uneviscerated fish can harbor harmful bacteria and parasites that may cause serious illness if not completely removed during cleaning and cooking.
- 2026-03-04FDA-FoodGerber Products Company dba Nestle Infant NutritionClass IINationwideGerber Arrowroot Biscuits, Net Wt. 5.5 oz. (155g), packaged in a plastic resealable bag with UPC 015000005962, packed 4 bags/case with UPC 015000935726; Made for Gerber Products Co., Fremont, MI 49413
Downstream recall. Product contains arrowroot flour ingredient that was voluntarily recalled by the supplier due to potential contamination of soft kraft paper/plastic bag pieces.
- 2026-03-04FDA-DrugWizcure PharmaClass IINationwideStop using BioGlo Fluorescein Sodium eye strips
BioGlo Fluorescein Sodium Ophthalmic Strips were not manufactured according to safety standards, raising concerns about sterility. The strips are used by eye care professionals for diagnostic eye exams. All lots distributed nationwide are affected.
- 2026-03-04FDA-DrugWizcure PharmaClass IINationwideStop using Bio Glo Fluorescein Sodium strips
Bio Glo Fluorescein Sodium Ophthalmic Strips USP were not manufactured following proper sterility standards. These diagnostic strips, distributed nationwide, may not be sterile and could pose a safety risk if used in the eye.
- 2026-03-04FDA-DrugWizcure PharmaClass IINationwideStop using Wizcure Fluorescein Sodium eye strips
Wizcure Fluorescein Sodium Ophthalmic Strips (1mg) were not manufactured following proper sterilization standards. These strips are used by eye care professionals to examine the eye surface. Because sterility cannot be assured, there is a potential risk of contamination.
- 2026-03-04FDA-DrugWizcure PharmaClass IINationwideStop using Vista Gonio Eye Lubricant
Vista Gonio Eye Lubricant (hypromellose ophthalmic solution) distributed by hi-health was not manufactured following required safety standards, raising concerns about sterility. All lots of this eye drop product are affected. No injuries have been reported to date.
- 2026-03-04FDA-DrugWizcure PharmaClass IINationwideStop using Vista Meibo Tears eye drops
Vista Meibo Tears Propylene Glycol 0.6% eye drops were not manufactured under proper safety conditions, raising concerns about sterility. The FDA issued a recall of all lots distributed nationwide. No injuries have been reported.
- 2026-03-04FDA-DrugWizcure PharmaClass IINationwideStop using Vista Gel eye drops
Vista Gel Hypromellose eye drops were not manufactured according to FDA safety standards, which means the product may not be sterile. The eye drops were distributed nationwide in the United States. No injuries have been reported.
- 2026-03-04FDA-DrugWizcure PharmaClass IINationwideStop using Vista Tears eye drops
Vista Tears eye drops were manufactured without proper sterility controls, which means they may not be safe for use in the eye. No injuries have been reported, but the product does not meet FDA safety standards.
- 2026-03-04FDA-DrugAgeboxClass IINationwideStop using Agebox iKids-Growth Night Formula
Agebox iKids-Growth Night Formula contains ibutamoren, a substance not listed on the label or approved by the FDA for this product. The affected 60-count bottles were sold online through Agebox.com and Amazon.com. No injuries have been reported.
- 2026-03-04FDA-DrugAgeboxClass IINationwideStop using Agebox iKids-Growth capsules
Agebox iKids-Growth Day Formula capsules contain an undeclared drug ingredient called ibutamoren that was not approved by the FDA. The product was sold without proper FDA authorization. This affects 60-count bottles with lot numbers 23101201, 24080801, and 25020701.
- 2026-03-04FDA-DrugSlate Run PharmaceuticalsClass IIINationwideCheck Slate Run Eptifibatide Injection labeling
Slate Run Pharmaceuticals is recalling Eptifibatide Injection 75 mg/100 mL vials because the carton label says "weight-adjusted bolus dosing" when it should say "weight-adjusted infusion." This labeling error could lead to incorrect administration of the medication. No injuries have been reported.
- 2026-03-04FDA-DrugAvKAREClass IINationwideStop using AvKARE Amantadine HCl capsules
AvKARE is recalling one lot of Amantadine HCl 100 mg capsules because they failed to meet dissolution specifications—meaning the capsules may not break down properly in the body, affecting how much medicine you receive. This is a quality issue identified during manufacturing testing. No injuries have been reported.
- 2026-03-04FDA-DrugLeo PharmaClass IINationwideStop using recalled Adbry injection lots
LEO Pharma is recalling specific lots of Adbry, a prescription injection used to treat atopic dermatitis, because one unit was found to contain wool fiber particles. This contamination raises concerns about sterility and safety. No injuries have been reported so far.
- 2026-03-03USDAClass INationwideThrow out recalled Ajinomoto frozen Asian food products
Ajinomoto Foods North America is recalling frozen fried rice, ramen, and shu mai (dumpling) products sold under Ajinomoto, Kroger, Ling Ling, Tai Pei, and Trader Joe's brand names due to possible glass fragments in the food. The glass came from carrots used in the products. No injuries have been reported so far.
- 2026-03-01USDAPublic Health AlertNationwideThrow out beef jerky with undeclared soy
Several beef jerky products sold in Hawaii and online contain soy lecithin that is not listed on the label. Soy is a common allergen that can cause serious reactions in people with soy allergies. The products are no longer being sold, but some may still be in home pantries.
- 2026-02-26CPSCEvajoyNationwideStop using Evajoy above-ground pools
Evajoy above-ground pools 48 inches tall or larger have a compression strap around the outside legs that can act as a foothold, allowing children to climb into the pool. This creates a drowning risk even if the ladder is removed.
- 2026-02-26CPSCHisenseNationwideStop using Babysense Max View monitor display
The display unit (parent unit) of Babysense Max View Baby Monitors can overheat or spark while charging, creating a fire risk. The affected model is VBM55, sold online from January 2023 through December 2025. Hisense has received 11 reports of overheating or sparking, but no injuries so far.
- 2026-02-26CPSCAndersenNationwideStop using Andersen Windows opening control devices
Andersen Windows is recalling opening control devices on 100 Series casement windows manufactured before November 19, 2025. These devices can break or detach after impact, allowing windows to open unexpectedly and creating a fall risk, especially for children. No injuries have been reported, but eight instances of device failure have been documented.
- 2026-02-26CPSCSumDirectNationwideStop using SumDirect LED mini lights
SumDirect LED mini lights contain small button cell batteries that children can easily remove and swallow, causing serious internal injuries or death. The product lacks required safety warnings and does not meet federal battery safety standards. About 1,600 units were sold online since 2016.
- 2026-02-26CPSCTodsonNationwideStop using Concord bike helmets immediately
Todson's Concord 360 Degree Rechargeable Light-Up bike helmets (size large, black with LED lights) do not meet federal safety standards for retention and fit. The helmets may fail to stay in place or protect your head during a crash, creating a serious injury risk.
- 2026-02-26CPSCIndream StoreNationwideStop using Joyreal busy board toys
Joyreal busy board toys sold on Amazon have a small mirror that can detach, creating a choking hazard for children. The mirror also has sharp edges that can cause cuts. About 210 units were sold between September and November 2025.
- 2026-02-26CPSCnbplusNationwideStop using Zelbuck chess games immediately
Zelbuck children's chess games contain loose magnets that can come out and be swallowed by children. When high-powered magnets are ingested, they can stick together inside the stomach or intestines, causing serious blockages, tears, or life-threatening infections.
- 2026-02-26CPSCTheKiddoSpaceStoreNationwideStop using TheKiddoSpace sensory swing
TheKiddoSpace's cocoon-style sensory swing can form loops with its fabric that may wrap around a child's head or neck, creating a strangulation risk. About 140 swings were sold online between November 2023 and February 2025. No injuries have been reported yet.
- 2026-02-26CPSCTheKiddoSpaceStoreNationwideStop using TheKiddoSpace Christmas tree toy
TheKiddoSpace children's Christmas tree play sets contain dangerous levels of lead in the zipper pull on the music box compartment. Lead can poison young children if ingested. The toy also fails to meet safety standards for battery-operated toys.
- 2026-02-26CPSCTheKiddoSpaceStoreNationwideStop using TheKiddoSpace peg dolls immediately
TheKiddoSpace peg dolls in cups toys contain small wooden pieces that can block a child's airway. These toys are intended for children under three years old but violate federal small parts safety rules. About 40 of these toys were sold online between July 2023 and February 2025.
- 2026-02-26CPSCTheKiddoSpaceStoreNationwideStop using TheKiddoSpace LED soccer hover balls
TheKiddoSpace LED soccer hover balls have batteries that get too hot and can cause burns. The company received three reports of a burning smell during use. About 650 small hover balls (5.5 inches diameter) with black and white design and foam bumpers are affected.
- 2026-02-26CPSCTheKiddoSpaceStoreNationwideStop using TheKiddoSpace egg puzzle toys
TheKiddoSpace recalled children's Montessori puzzle eggs because the egg pieces can block a child's airway. The toys were sold online from June 2023 through February 2025. No injuries have been reported, but the risk to young children is serious.
- 2026-02-26CPSCTheKiddoSpaceStoreNationwideTheKiddoSpace Recalls Children's Flashcard Talking Toys Due to Risk of Injury from Lead and Phthalate Exposure; Violates Federal Lead Content and Phthalates Bans and Standard for Toys
The recalled children's flashcard toy sets contain levels of lead that exceed the federal lead content ban and levels of phthalates that exceed the federal phthalates ban. Lead and phthalates are toxic if ingested by young children and can cause adverse health issues. In addition, the flashcards also violate the mandatory standard for toys because they fail to comply with the short circuit protection requirement for battery-operated toys.
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