State

Arizona product recalls

73,388 recalls have nationwide distribution and so reach Arizona. 8,387 additional recalls listed Arizona specifically in their distribution scope.

What the numbers show

Total: 8,387
Critical: 1,313
Severe: 2,047
Most recent: 2026-10-02

Of the 8,387 recalls naming Arizona we have scored against our rubric, 1,313 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,047 (24%) are Severe.

Which agencies issued them

These figures cover only the 8,387 recalls whose distribution notice names Arizona specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

21651–21675 of 81775

HighCPSC·22175·2022-06-30
RIO-Branded Swinging Hammock Chairs Recalled Due to Collapse Injury Hazard
ShelterLogic Group is recalling approximately 786,000 RIO-branded swinging hammock chairs because improper pin insertion during assembly can cause the chair's legs to collapse, injuring users. The company has received 24 reports of injuries including bruises, lacerations, concussions, and back strain.
Product
RIO-branded Swinging Hammock Chairs
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·22754·2022-06-30
Mohnark Lidocaine 4% Topical Anesthetic Cream Recalled for Non-Child-Resistant Packaging
Mohnark Pharmaceuticals is recalling Lidocaine 4% Topical Anesthetic Cream because the packaging does not meet child-resistant requirements, creating a poisoning risk if young children ingest the product. About 9,000 units sold online were affected.
Product
Lidocaine 4% Topical Anesthetic Cream
Category
Drug
Distribution
Distributed nationwide
HighCPSC·22176·2022-06-30
Laars Residential Gas-Fired Boilers Recalled for Carbon Monoxide Risk
Laars Heating Systems is recalling about 545 residential gas-fired boilers because a malfunctioning blocked vent temperature switch can release carbon monoxide into homes. No injuries have been reported.
Product
Residential atmospheric gas-fired boilers
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·22V465000·2022-06-30
GM Recalls 2018-2020 Buick Regal for Brake Software Error
General Motors is recalling 2018-2020 Buick Regal vehicles because a software error may cause loss of power brake assist, increasing stopping distance.
Product
BUICK — BUICK REGAL
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·22178·2022-06-30
Children's Nightgowns Recalled for Flammability Standards Violation
iMOONZZZ children's nightgowns sold on Amazon fail to meet federal flammability standards for sleepwear, posing a burn injury risk. About 2,000 units sold between June 2019 and May 2022 are affected.
Product
Children's Nightgowns
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·22V463000·2022-06-30
2022 Chevrolet Silverado 1500 accessory brake light may not function properly
General Motors is recalling certain 2022 Chevrolet Silverado and GMC Sierra trucks with an accessory sport bar. The high-mounted brake light may not function or may be blocked, reducing visibility to other drivers and increasing crash risk.
Product
GMC — GMC, CHEVROLET SIERRA 1500, SILVERADO 1500
Category
Vehicle
Distribution
Distributed nationwide
ModerateCPSC·22753·2022-06-30
Yamaha Kodiak 700 ATVs Recalled for Missing Load Limit Label
Yamaha is recalling about 3,500 Model Year 2021 and 2022 Kodiak 700 ATVs because they are missing the "Maximum Loading Limit" label, which can result in unsafe trailer towing and crash hazards.
Product
Model Year 2021 and 2022 Kodiak 700 All-Terrain Vehicles (ATVs)
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1339-2022·2022-06-29
Peanut Butter Fudge Recalled Due to Potential Salmonella Contamination
Calico Cottage Inc is recalling Peanuttiest Caramel Chocolate fudge nationwide because the peanut butter ingredient may be contaminated with Salmonella.
Product
1. PEANUTTIEST CARAMEL CHOCOLATE P-MADE(6SS)6LB NT WT - not consumer packaging, bulk carton
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1338-2022·2022-06-29
Peanut Butter Fudge Recalled for Potential Salmonella Contamination
Calico Cottage Inc is recalling peanut butter fudge products due to potential Salmonella contamination in the peanut butter ingredient. The recall affects bulk carton products distributed nationwide.
Product
1. PEANUT BUTTER FUDGE (3 - 6LB SLABS/CS) 18LB NET WT - not consumer packaging, bulk carton 2. PEANUT BUTTER FUDGE (6S) 6LB NET WT- not consumer packaging, bulk carton 3. PEANUT BUTTER FUDGE (6SS) 6LB NET WT- not consumer packaging, bulk carton
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1271-2022·2022-06-29
Medfusion Syringe Pump Recalled Due to Multiple Infusion Control and Alarm Failures
Smiths Medical recalled 58,671 Medfusion Syringe Pump units worldwide due to multiple failures that could interrupt therapy or cause over-infusion, including defective alarms and display errors.
Product
Medfusion Syringe Pump Model: Model 4000-0100-50, Model 4000-0101-249, Model 4000-0101-50, Model 4000-0101-51, Model 4000-0101-78, Model 4000-0105-249, Model 4000-0105-51, Model 4000-0105-78, Model 4000-0106-00, Model 4000-0106-01, Model 4000-0106-231
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1341-2022·2022-06-29
Black Sesame Mochi Lacks Undeclared Milk Powder Labeling
Mia's Bakery recalls Black Sesame Mochi (7 oz packages) because the product does not declare milk powder on its label, posing a risk to consumers with milk allergies.
Product
Mia's Bakery Black Sesame Mochi Wt. 7 oz./198.5 gram UPC: 8 50660 00009 0 Ings: Glutinous Rice Flour, Sugar, Mung Bean, Soy Bean Oil, Water, Sesame Oil, Sodium Benzoate, Black Color, FD & C Yellow 5 & 6, Red #4 and Blue #1. Keep refrigerated after opening 1965 Potrero…
Category
Food
Distribution
4 states
SevereFDA (Food)·F-1321-2022·2022-06-29
Chocolate Peanut Butter Cups Recalled for Salmonella Contamination
Albanese Confectionery Group recalls Rich's Milk Chocolate peanut butter cups nationwide due to Salmonella contamination from recalled Jif peanut butter used in manufacturing.
Product
Rich s Milk Chocolate Giant Layered Peanut Butter and Cups Rich s Milk Chocolate Mini Peanut Butter Cups; 2ct 5lb bulk per 10 lb case. Product not retail packaged, distributed for bulk sale at retail.
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1337-2022·2022-06-29
Chocolate fudge with peanut butter recalled for potential Salmonella
Calico Cottage Inc is recalling chocolate fudge products containing peanut butter due to potential Salmonella contamination. The recall affects 677 units distributed nationwide.
Product
1. PEANUT BUTTER CHOC (3 - 6LB SLABS/CS) 18LB NET WT - Not consumer packaging, bulk carton 2. PEANUT BUTTER CHOC FUDGE LAYERED (6S) 6LB NET WT - not consumer packaging, bulk carton 3. PEANUT BUTTER CHOCOLATE FUDGE (6SS) 6LB NET WT - not consumer packaging, bulk carton
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1272-2022·2022-06-29
Medfusion Syringe Pump Class I Recall: Risk of Over-Infusion or Therapy Interruption
Smiths Medical is recalling multiple Medfusion Syringe Pump models due to software and hardware defects that may interrupt drug infusion or cause over-infusion. Approximately 65,093 units distributed worldwide are affected.
Product
Medfusion Syringe Pump Models: 3500, 3500-0600-00, 3500-0600-01, 3500-0600-249, 3500-0600-50, 3500-0600-51, 3500-0600-82, 3500-306, 3500-402, 3500-414, 3500-415, 3500-500, 3500BC, 3500E, 3500G, 3500SD, 3500SD-500, 3500VX, 3500VX-306, 3500VX-414, 3500VX-415, 3500VX-500, 3500ZE…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1266-2022·2022-06-29
HeartWare HVAD Battery Model 1650DE May Malfunction Due to Weld Defect
Medtronic is recalling HeartWare HVAD batteries (Model 1650DE) due to an internal weld defect that can cause battery malfunction and prevent proper charging. Approximately 429 affected batteries were distributed worldwide.
Product
HeartWare Battery, Model #1650DE, a component of the HeartWare Ventricular Assist Device (HVAD) System.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1320-2022·2022-06-29
JR Simplot Frozen French Fries Recalled for Undeclared Wheat
JR Simplot Food Group is recalling bulk frozen french fries (Shoestring 1/4" Grade A Fancy Fry, lot code 200 APR 17 22) due to undeclared wheat. Approximately 3,207 cases were distributed wholesale to food service customers in 12 states.
Product
Bulk, frozen french fries as Shoestring 1/4" Frozen Grade A Fancy Fry packed in clear poly bag with lot code "200 APR 17 22" and packed in cardboard case that is labeled in part, "Bountiful HARVEST***ORIGINALS SHOESTRING 1/4" FROZEN GRADE A FANCY FRY NO ARTIFICIAL FLAVORS OR…
Category
Food
Distribution
12 states
SevereFDA (Food)·F-1340-2022·2022-06-29
Salted Nut Roll Fudge Recalled for Potential Salmonella in Peanut Butter
Calico Cottage Inc is recalling Salted Nut Roll Pre-Made Fudge nationwide because the peanut butter ingredient is potentially contaminated with Salmonella.
Product
1. SALTED NUT ROLL PRE-MADE FUDGE (6SS) 6LB NET WT - not consumer package, bulk carton
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1274-2022·2022-06-29
Colonovideoscope Model CF-H180AL recalled due to narrowed viewing angle
Olympus Corporation recalls a single colonovideoscope model CF-H180AL because an incorrect camera unit was installed, causing narrower viewing angle and potential device protrusion that could injure tissue. No injuries have been reported.
Product
Colonovideoscope Model CF-H180AL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1156-2022·2022-06-29
Tretinoin Capsules Recalled Nationwide for Failed Dissolution Specifications
Teva Pharmaceuticals is recalling Tretinoin Capsules (10 mg) nationwide due to failed dissolution specifications that may affect medication effectiveness. Patients should contact their pharmacist or doctor to confirm if their prescription is affected.
Product
Tretinoin Capsules, 10 mg, Rx Only, 100 capsules per bottle, Teva Pharmaceuticals USA Inc., North Wales, PA, 19454, NDC 0555-0808-02.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1153-2022·2022-06-29
Testosterone Cypionate Injectable Recalled for Manufacturing Quality Issues
Sun Pharmaceutical recalls 97,450 vials of Testosterone Cypionate Injection nationwide due to manufacturing deviations that could cause out-of-specification impurities.
Product
TESTOSTERONE CYPIONATE — TESTOSTERONE CYPIONATE (TESTOSTERONE CYPIONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1154-2022·2022-06-29
Testosterone Cypionate Injectable Recalled Due to Manufacturing Sterility Deviation
Sun Pharmaceutical is recalling approximately 47,500 vials of Testosterone Cypionate Injection due to a manufacturing deviation that may have affected product sterility.
Product
TESTOSTERONE CYPIONATE — TESTOSTERONE CYPIONATE (TESTOSTERONE CYPIONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1322-2022·2022-06-29
Trader Joe's Chopped Salad Recalled Due to Undeclared Peanut Allergen
Taylor Farms is recalling Trader Joe's BBQ & Black Pepper Toscano Chopped Salad because it contains undeclared peanuts and peanut lime dressing due to an incorrect master pack. The product poses a risk to consumers with peanut allergies.
Product
Trader Joe's BBQ & Black Pepper Toscano Chopped Salad 11 oz. Contains Milk, Soy, Wheat Dist. & Sold Exclusively By: Trader Joe's, Monrovia, CA 91016
Category
Food
Distribution
43 states
HighFDA (Food)·F-1345-2022·2022-06-29
Ice cream recall for undeclared tree nut allergen
Red Button Vintage Creamery Canadian Vanilla Ice Cream was distributed nationwide with undeclared almond allergen due to packaging mix-up. Consumers with tree nut allergies should not consume this product.
Product
Red Button Vintage Creamery Canadian Vanilla Ice Cream, 56 ounce tub, UPC 0 77865 01001 7, Distributed by Associated Foods Stores, Salt Lake City, UT, 84119. Store Frozen.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1273-2022·2022-06-29
FDA Recalls Catheter Drainage Kits With Wrong Needle Size
Bard Peripheral Vascular Inc is recalling certain catheter drainage kits that may contain an 8 Fr needle instead of the correct 6 Fr needle. The incorrect needle size could cause tissue injury during patient care.
Product
REF: PIG1260K, 6Fr, X10, Safe-t-Centesis Catheter drainage Kit, Sterile EO,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1347-2022·2022-06-29
Kava Glycerite Recalled Due to High Yeast and Mold Contamination
EarthLab Inc is recalling Wise Woman Herbals Standardized Kava Glycerite due to high yeast and mold counts detected during microbial testing. The affected product was distributed nationwide.
Product
Wise Woman Herbals Standardized Kava Glycerite, product is liquid and contains 15 mg Kavalactones (from Piper methysticum) and 9 mg Kavalactones (from Piper methysticum) depending on lot. Dosage: 60 drops 1-2 times a day. Product is packaged in Amber Glass Boston Round…
Category
Food
Distribution
Distributed nationwide