State

Arizona product recalls

73,503 recalls have nationwide distribution and so reach Arizona. 8,390 additional recalls listed Arizona specifically in their distribution scope.

What the numbers show

Total: 8,390
Critical: 1,313
Severe: 2,047
Most recent: 2026-10-14

Of the 8,390 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 8,390 recalls whose distribution notice names Arizona specifically. The 73,503 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25151–25175 of 81893

HighFDA (Food)·F-0052-2022·2021-10-27
Rice Crispy Treats Recalled for Undeclared Milk and Soy Allergens
Chocolate & the Chip is recalling The Sweetie Rice Crispy treats due to undeclared milk and soy allergens found during inspection. The products were distributed nationwide.
Product
Chocolate & the Chip The Sweetie Rice Crispy: Rice crispy treats: 6 oz / 171 grams Packaged in a food grade clear poly tubing, heat sealed with label Corrected Ingredients: Not provided Labels found during the inspection had undeclared milk, soy. Firm had listed…
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0158-2022·2021-10-27
Medtronic surgical blades recalled for tip breaks and vibration
Medtronic recalls 274,991 sterile surgical blades due to complaints of tip breaks and vibration during use. The blades are components of surgical systems used in brain and ENT procedures.
Product
Medtronic Sterile single-use blades that are components of the StraightShot M Series Handpiece and Fusion ENT Navigation Software, and the Midas Rex Microsaw and Triton System with the following product numbers: (1) REF 40A2500, Nucleus Removal Angled Blade, 25 cm x 4.0 mm…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0124-2022·2021-10-27
Atellica IM 1300 Analyzer Reagent Overflow at High Altitudes
Siemens has recalled approximately 1,193 Atellica IM 1300 analyzers due to reagent overflow that occurs at altitudes above 350 meters, causing diagnostic test errors.
Product
Atellica IM 1300 Analyzer, SMN 11066001
Category
Medical Device
Distribution
23 states
HighFDA (Devices)·Z-0138-2022·2021-10-27
GE Healthcare SIGNA Voyager MRI System Recall for Missing Image Slices
GE Healthcare is recalling the SIGNA Voyager nuclear magnetic resonance imaging system due to a software issue that can cause missing slices in 3D volume images, potentially creating gaps in anatomical information.
Product
SIGNA Voyager nuclear magnetic resonance imaging system
Category
Medical Device
Distribution
19 states
HighCPSC·22011·2021-10-27
Magnussen Home Nova Series 5-Drawer Chests Recalled for Tip-Over Hazard
Magnussen Home is recalling about 13,200 Nova Series 5-Drawer Chests sold from August 2009 through August 2015 because they can tip over and cause entrapment hazards to children if not anchored to the wall.
Product
Nova Series 5-Drawer Chests
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Food)·F-0050-2022·2021-10-27
Chocolate & the Chip Brown Butter Rice Crispy Treats Recalled for Undeclared Milk
Chocolate and the Chip is recalling Brown Butter Rice Crispy Treat products due to undeclared milk allergen on labels. The products were distributed nationwide and manufactured between July 1 and September 30, 2021.
Product
Chocolate & the Chip Brown Butter Rice Crispy Treat - Chocolate: Rice crispy treats: 6 oz / 171 grams Packaged in a food grade clear poly tubing, heat sealed with label Corrected Ingredients: Ingredients: rice cereal (rice, sugar, malt extract, salt, preservative…
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0136-2022·2021-10-27
GE Discovery MR750 MRI System May Produce Incomplete Diagnostic Images
GE Healthcare's Discovery MR750 3.0T MRI system may not capture all required image slices under certain conditions, resulting in gaps in diagnostic 3D images. Five devices are affected.
Product
Discovery MR750 3.0T nuclear magnetic resonance imaging system
Category
Medical Device
Distribution
19 states
HighNHTSA·21V840000·2021-10-27
Hyundai recalls 2021 Palisade for brake fluid contamination
Brake fluid contamination in certain 2021 Hyundai Palisades can reduce braking performance and increase crash risk. Owners should contact Hyundai for a free brake system repair.
Product
HYUNDAI — HYUNDAI PALISADE
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·22010·2021-10-27
Liberty Hardware Glass Cabinet Knobs Recalled for Laceration Hazard
Liberty Hardware is recalling about 38,000 glass cabinet knobs because the glass stem can break during use, causing laceration injuries. Consumers should stop using the knobs and contact Liberty Hardware for a refund.
Product
Glass cabinet knobs
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Food)·F-0028-2022·2021-10-27
Chocolate & the Chip Cookies Recalled for Undeclared Allergens
Chocolate & the Chip Original Cookies are being recalled due to undeclared allergens including wheat, milk, soy, and tree nuts (hazelnuts) found during a California Department of Public Health inspection. Consumers with allergies to these substances should not consume the product.
Product
Chocolate & the Chip The Original Cookies: 4 oz / 114 grams per pack. Cookies are packaged in uniform pairs in a food grade clear resealable bag and label Corrected Ingredients: Original chocolate chip cookie: Ingredients: All purpose flour (bleached wheat flour, malted barley…
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0033-2022·2021-10-27
Chocolate & the Chip Cookies Recalled for Undeclared Allergens
Chocolate & the Chip is recalling Fluffadoodle and Fluffa-Nutta Cookies due to undeclared wheat, milk, and soy allergens found on packaging labels during a California health inspection.
Product
Chocolate & the Chip Fluffadoodle and Fluffa-Nutta Cookies: 4 oz / 114 grams per pack. Cookies are packaged in uniform pairs in a food grade clear resealable bag and label Corrected Ingredients: Ingredients: All purpose flour (bleached wheat flour, malted barley flour…
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0135-2022·2021-10-27
Discovery MR750w 3.0T MRI: Missing Image Slices in 3D Volume
GE Healthcare recalls the Discovery MR750w 3.0T MRI system. Under certain software conditions, image slices may be missing, creating gaps in 3D diagnostic images.
Product
Discovery MR750w 3.0T nuclear magnetic resonance imaging system
Category
Medical Device
Distribution
19 states
HighFDA (Food)·F-0036-2022·2021-10-27
Chocolate & the Chip Octoberfest Cookies Recalled for Undeclared Allergens
Chocolate & the Chip Octoberfest Cookies are being recalled due to undeclared wheat, milk, and soy allergens found on product labels during a California Department of Public Health inspection.
Product
Chocolate & the Chip Octoberfest Cookies: 4 oz / 114 grams per pack. Cookies are packaged in uniform pairs in a food grade clear resealable bag and label Corrected Ingredients: Not provided. Labels found during the inspection had undeclared wheat, milk, soy. Firm had listed…
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0042-2022·2021-10-27
Chocolate & the Chip Lavender Cookies Recalled for Undeclared Allergens
Chocolate & the Chip is recalling Lavender chocolate chip cookies due to undeclared wheat, milk, and soy allergens found on product labels during a California Department of Public Health inspection.
Product
Chocolate & the Chip Lavender chocolate chip cookies: Cookies: 4 oz / 114 grams per pack. Cookies are packaged in uniform pairs in a food grade clear resealable bag and label Corrected Ingredients: Ingredients: All purpose flour (bleached wheat flour, malted barley flour…
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0134-2022·2021-10-27
GE SIGNA Pioneer MRI Recall for Missing Image Slices
GE Healthcare is recalling 5 SIGNA Pioneer MRI systems where a software issue can cause missing image slices in 3D volume scans. This may lead to diagnostic gaps.
Product
SIGNA Pioneer nuclear magnetic resonance imaging system
Category
Medical Device
Distribution
19 states
ModerateFDA (Drugs)·D-0015-2022·2021-10-27
Coppertone Pure & Simple 50 Sunscreen Spray Recall for cGMP Deviations
Beiersdorf Inc. is recalling Coppertone Pure & Simple 50 Sunscreen Spray due to manufacturing practice deviations. Approximately 36,660 cans were distributed nationwide.
Product
Coppertone Pure & Simple 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%, NET WT 5 OZ (142 g) can, Beiersdorf Inc., Wilton, CT 06897 UPC 0 72140 02880 0
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0019-2022·2021-10-27
Rocuronium Bromide Injection Lacks Paralyzing Agent Warning
Piramal Critical Care is recalling Rocuronium Bromide Injection because the finished product vial lacks the required "WARNING: PARALYZING AGENT" statement on the flip cap. The missing warning could lead to unsafe use of this prescription neuromuscular-blocking drug.
Product
Rocuronium Bromide Injection 50mg/5 mL, 5mL Multi-Dose Vial, Rx only, Manufactured for: Piramal Critical Care, Bethlehem, PA 18017, USA, Manufactured by: Sanovel Ilac, San. Ve Tic. A.S. Istanbul, Turkey, NDC 66794-0228-41
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0120-2022·2021-10-27
Diagnostic Control Material Outside Expected Range, Potential for Delayed Results
Ortho Clinical Diagnostics is recalling VITROS Anti-SARS-CoV-2 Immunodiagnostic Controls that may be outside the expected control range, potentially delaying diagnostic test results in laboratory systems.
Product
VITROS Immunodiagnostic Products Anti-SARS-CoV-2 IgG Quantitative Controls (IVD)- For use in monitoring the performance of the VITROS ECi/ECiQ/3600 Immunodiagnostic Systems and the VITROS 5600/XT 7600 Integrated Systems when used with the VITROS Immunodiagnostic Products…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0022-2022·2021-10-27
AirDuo Digihaler 232/14 Inhalation Powder Subpotent Recall
Teva Pharmaceuticals is recalling AirDuo Digihaler 232/14 inhalation powder because some units do not deliver the correct amount of salmeterol as labeled.
Product
AirDuo Digihaler 232/14 (fluticasone propionate 232 mcg and salmeterol 14 mcg) Inhalation Powder, Sample Not For Sale, Rx Only, Mktd by: Teva Respiratory, LLC, Frazer, PA 19355, Manufactured in Ireland, NDC 59310-530-08.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0025-2022·2021-10-27
AirDuo Digihaler 232/14 Inhalation Powder Recall for Subpotent Salmeterol
Teva Pharmaceuticals is recalling approximately 5,500 units of AirDuo Digihaler 232/14 inhalation powder distributed nationwide because some inhalers contain less salmeterol than the labeled dose.
Product
AirDuo Digihaler 232/14 (fluticasone propionate 232 mcg and salmeterol 14 mcg) Inhalation Powder, Rx Only, Mktd by: Teva Respiratory, LLC, Frazer, PA 19355, Manufactured in Ireland, NDC 59310-136-06
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0143-2022·2021-10-27
Smith & Nephew cannulated screw label incorrectly indicates threading type
Smith & Nephew is recalling 6.5mm x 165mm cannulated screws because the product label incorrectly states the screws are fully threaded when they are actually partially threaded.
Product
6.5MMX165MM CANNULATED SCREW
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0017-2022·2021-10-27
Coppertone Pure & Simple Baby 50 Sunscreen Spray Recalled for cGMP Deviations
Beiersdorf Inc. is recalling 14,748 cans of Coppertone Pure & Simple baby 50 Sunscreen Spray due to cGMP (current Good Manufacturing Practice) deviations. The product was distributed nationwide.
Product
Coppertone Pure & Simple baby 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%, NET WT 5 OZ (142 g) can, Beiersdorf Inc., Wilton, CT 06897 UPC 0 72140 02881 7
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0026-2022·2021-10-27
Omeprazole Magnesium Acid Reducer Capsules Recalled for Staple Contamination
Dr. Reddy's Laboratories is recalling Acid Reducer (Omeprazole Magnesium) 20 mg capsules nationwide because staples have been found co-mingled with capsules in bottles.
Product
ACID REDUCER — ACID REDUCER (OMEPRAZOLE MAGNESIUM)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0024-2022·2021-10-27
AirDuo Digihaler inhalation powder subpotent drug recall
Teva Pharmaceuticals is recalling AirDuo Digihaler 113/14 inhalation powder because some batches do not deliver the labeled amount of salmeterol, a critical active ingredient for asthma and COPD control.
Product
AirDuo Digihaler 113/14 (fluticasone propionate 113 mcg and salmeterol 14 mcg) Inhalation Powder, Rx Only, Mktd. by: Teva Respiratory, LLC, Frazer, PA 19355, Manufactured in Ireland, NDC 59310-129-06.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0151-2022·2021-10-27
HemosIL Liquid Anti-Xa Assay On-Board Stability Issue Recall
Instrumentation Laboratory is recalling HemosIL Liquid Anti-Xa, a coagulation assay measuring heparin activity, due to reduced on-board instrument stability from 7 days to 5 days.
Product
HemosIL Liquid Anti-Xa- Automated chromogenic assay for the quantitative determination of unfractionated heparin (UFH) and low molecular weight heparin (LMWH) activity in human citrated plasma on IL Coagulation Systems, (ACLTOP¿ Family, ACL TOP Family 50 Seriest and ACL…
Category
Medical Device
Distribution
Distributed nationwide