State

Arizona product recalls

73,088 recalls have nationwide distribution and so reach Arizona. 8,385 additional recalls listed Arizona specifically in their distribution scope.

What the numbers show

Total: 8,385
Critical: 1,313
Severe: 1,719
Most recent: 2026-09-23

Of the 8,385 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 1,719 (21%) are Severe.

Which agencies issued them

These figures cover only the 8,385 recalls whose distribution notice names Arizona specifically. The 73,088 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

9326–9350 of 81473

HighFDA (Drugs)·D-0049-2025·2024-11-27
Guaifenesin-Dextromethorphan Cough Syrup Recalled for Failed Impurity Specifications
Major Pharmaceuticals is recalling Guaifenesin Dextromethorphan Syrup nationwide for specific lots that failed to meet impurity and degradation specifications. Consumers should contact their pharmacist if they possess affected lots.
Product
Guaifenesin Dextromethorphan Syrup, 200 mg/20mg per 10 mL, Major Pharmaceuticals 8401 Bearing Drive, Suite 100, Indianapolis, IN, 46268, NDC 0904-7135-72
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0054-2025·2024-11-27
Ramipril Capsule Medication Recalled Over Unapproved Vendor Manufacturing Deviations
Lupin Pharmaceuticals is recalling 357,414 bottles of Ramipril 10 mg capsules due to CGMP deviations where the active pharmaceutical ingredient was sourced from an unapproved vendor. The affected product was distributed to 30 wholesalers with potential nationwide distribution.
Product
RAMIPRIL — RAMIPRIL (RAMIPRIL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0468-2025·2024-11-27
Posi-Stop Injection Needles Recalled for Manufacturing Debris Blocking Flow
Hobbs Medical is recalling Posi-Stop Injection Needles because manufacturing debris blocks the needle, preventing injection solutions from flowing properly. The 70 affected units were distributed to healthcare facilities in multiple U.S. states and Canada.
Product
Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4720
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0476-2025·2024-11-27
FDA Recalls Posi-Stop Injection Needles Due to Manufacturing Debris
Hobbs Medical is recalling Posi-Stop Injection Needles (25 gauge) because some units contain debris in the needle shaft that blocks injection solution flow.
Product
Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4723
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0471-2025·2024-11-27
Injection Needles Recalled for Manufacturing Debris Blocking Medication Flow
Hobbs Medical is recalling Posi-Stop Injection Needles due to manufacturing debris inside the needle shaft that blocks medication flow. The affected lot was distributed across multiple US states and Canada.
Product
Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4716
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0376-2025·2024-11-27
Baxter MiniCap PD Transfer Set Recalled for Potential PCB Exposure
Baxter is recalling MiniCap Extended Life PD Transfer Sets due to potential exposure to non-dioxin-like polychlorinated biphenyls.
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4483; use in Peritoneal Dialysis
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0052-2025·2024-11-27
FDA recalls Ramipril 2.5 mg capsules for manufacturing control deviations
Lupin Pharmaceuticals is recalling Ramipril 2.5 mg capsules after sourcing the active ingredient from an unapproved vendor. Approximately 112,770 bottles were distributed to wholesalers nationwide.
Product
RAMIPRIL — RAMIPRIL (RAMIPRIL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0474-2025·2024-11-27
Posi-Stop Injection Needles Recalled Due to Manufacturing Debris Blocking Injection Flow
Hobbs Medical recalls Posi-Stop injection needles because manufacturing debris can block the needle, preventing injection solutions from flowing properly. Affected units were distributed across multiple US states and Canada.
Product
Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4718
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0473-2025·2024-11-27
Posi-Stop Injection Needles recalled for manufacturing debris blockage
Hobbs Medical is recalling Posi-Stop Injection Needles due to manufacturing debris that can block needle flow. Some units may contain debris in the inner sheath that prevents injection solutions from functioning properly.
Product
Posi-Stop Injection Needle, 25 Gauge, Catalog Number: 4704
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0140-2025·2024-11-27
Great Value Cheese Danish Recalled for Plastic Pieces
Great Value Cheese Danish is being recalled due to plastic pieces found in the product. Consumers who purchased this item should discard it.
Product
Great Value Cheese Danish 16.5 oz UPC 078742201177, 12 retail units per case
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0488-2025·2024-11-27
EnChroma Safety Glasses recalled for defective impact protection
EnChroma Inc recalls 53 units of safety glasses with Rx indoor lenses that fail impact safety standards, posing a risk of eye injury. Affected models include Martinez Cx1 Indoor Rx, Summit Indoor Rx, and Martinez Black Cx Rx.
Product
EnChroma Safety Glasses with Rx Indoor Universal Lenses: Martinez Cx1 Indoor Rx, SKU: Cx.PC.IN.MTZ.BK.Rx; Summit Indoor Rx, Cx.PC.IN.SUM.BK.Rx; Martinez Black Cx Rx, Cx-3.PC.PT.MTZ.BK.Rx
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0374-2025·2024-11-27
Baxter MiniCap Peritoneal Dialysis Transfer Set Recalled for Chemical Exposure Risk
Baxter is recalling MiniCap Extended Life PD Transfer Sets due to potential exposure to polychlorinated biphenyls found in similar devices.
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482EJ; use in Peritoneal Dialysis
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0477-2025·2024-11-27
JuggerLoc/ToggleLoc 2.9mm Drill Guide Warping in Packaging
Biomet's JuggerLoc/ToggleLoc 2.9mm Drill Guide may warp when removed from packaging, potentially extending surgical time or causing tissue damage requiring intervention.
Product
JuggerLoc/ToggleLoc 2.9mm Drill Guide, Model number 110027357
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0141-2025·2024-11-27
Great Value Cinnamon Rolls Recalled for Plastic Contamination Nationwide
The JM Smucker Company is recalling Great Value Cinnamon Rolls nationwide due to possible plastic pieces in the product. Consumers should not consume affected units.
Product
Great Value Cinnamon Rolls 16.5oz UPC 078742201160, 12 retail units per case
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0061-2025·2024-11-27
Lisinopril 10 mg Tablets Recalled for Metal Fragment Contamination
Evaric Pharmaceuticals is recalling Lisinopril 10 mg tablets after a metal fragment was found embedded in a tablet. The affected lot (241103) was distributed nationwide; contact your pharmacist if you have this medication.
Product
LISINOPRIL — LISINOPRIL (LISINOPRIL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0380-2025·2024-11-27
Baxter MiniCap Peritoneal Dialysis Transfer Set Recalled for Chemical Exposure Risk
Baxter is recalling MiniCap Extended Life PD Transfer Sets due to potential exposure to non-dioxin-like polychlorinated biphenyls.
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4484; use in Peritoneal Dialysis
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0381-2025·2024-11-27
Baxter MiniCap PD Transfer Set Recalled for Potential Chemical Exposure Risk
Baxter is recalling MiniCap Extended Life PD Transfer Sets due to potential exposure to polychlorinated biphenyls.
Product
Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number T5C4482; use in Peritoneal Dialysis
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0470-2025·2024-11-27
Posi-Stop Injection Needle Recall Due to Manufacturing Debris
Hobbs Medical is recalling Posi-Stop Injection Needles (23 Gauge, Catalog 4706) due to manufacturing debris in the inner sheath that can block the needle and prevent injection solution flow.
Product
Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4706
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0485-2025·2024-11-27
Acrobat SUV Vacuum Stabilizer System Sterile Barrier Compromise Recall
Maquet Cardiovascular is recalling the Acrobat SUV Vacuum Stabilizer System (Model C-OM-9000Z) due to manufacturing deviations that compromise the sterile barrier. Sterility cannot be assured during the 2-year shelf life, affecting approximately 10,778 units.
Product
Acrobat SUV Vacuum Stabilizer System, ST. Model Number C-OM-9000Z
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0472-2025·2024-11-27
Posi-Stop Injection Needle Recalled Due to Manufacturing Debris Blockage
Hobbs Medical is recalling Posi-Stop Injection Needles (23 Gauge, Lot H11-23-057) because some units contain manufacturing debris that blocks the needle opening, preventing injection solutions from flowing properly.
Product
Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4721
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·24V898000·2024-11-27
Audi plug-in hybrid high voltage batteries can overheat
Volkswagen is recalling certain 2022-2023 Audi Q5 PHEV and 2022 Audi A7 PHEV vehicles because the high-voltage battery may overheat, increasing the risk of a fire.
Product
AUDI — AUDI Q5, A7
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0056-2025·2024-11-27
Vitamin D3 Dietary Supplement Recalled for Packaging Defect
Safecor Health is recalling specific lots of Vitamin D3 25 mcg tablets due to a manufacturing defect where blister card-foils may separate from the blister cavity. No illnesses or injuries have been reported.
Product
Vitamin D3, 25 mcg, 1 tablet in blister card-foils, 100-count unit dose box, www.safecorhealth.com, NDC 48433-104-01
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0498-2025·2024-11-27
Olympus Gastrointestinal Videoscope Drying Instructions Clarified
Olympus is recalling 1,749 GIF-1TH190 gastrointestinal videoscopes to clarify drying procedures in the instructions for use after human errors were identified during evaluation.
Product
Brand Name: EVIS EXERA III Gastrointestinal Videoscope GIF-1TH190 Product Name: Olympus GIF-1TH190 Model/Catalog Number: GIF-1TH190 Software Version: N/A Product Description: This instrument is intended to be used with an Olympus video system center, light source, documentati
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0058-2025·2024-11-27
Aspirin 81 mg chewable tablets recalled due to packaging defect
Safecor Health, LLC is recalling 1,470 boxes of Aspirin 81 mg chewable tablets nationwide due to a manufacturing defect where blister card-foils are separating from the blister cavity.
Product
ASPIRIN — ASPIRIN (ASPIRIN 81 MG)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0139-2025·2024-11-27
Dietary Supplement Recalled: Douglas Labs Stress-B-Plus Due to Niacin Form Mismatch
Nestle Health Science is recalling Douglas Labs Stress-B-Plus Dietary Supplement due to incorrect formulation. The product contains Niacin as Nicotinic acid but the label states Niacinamide.
Product
Douglas Labs Stress-B-Plus Dietary Supplement, Tablets, 90 tablets per bottle. UPC # 10539 97452, Lot Numbers ,50335944 and 50344396. Expiration Date 04/11/2026
Category
Drug
Distribution
35 states