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.

25626–25650 of 81893

SevereFDA (Drugs)·D-0805-2021·2021-09-22
AMINOSYN II 15% Amino Acid Injection Recalled for Particulate Matter
ICU Medical Inc is recalling AMINOSYN II 15% An Amino Acid Injection due to the presence of particulate matter including fibers, hair, and proteinaceous material found in retained samples.
Product
AMINOSYN II 15% An Amino Acid Injection, Sulfite-Free, 2000 mL in flexible containers, Rx ONLY, Hospira, Inc., Lake Forest, IL 60045. NDC 0409-7171-17
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0796-2021·2021-09-22
Florance Morris ANTISEPTIC Hand Sanitizer Recalled for Methanol Contamination
Florance Morris ANTISEPTIC Hand Sanitizer (70% ethyl alcohol) in 8.45 fl oz and 33.81 fl oz bottles is being recalled due to methanol contamination found in some lots. All lots are affected due to manufacturing under the same conditions as contaminated products.
Product
Florance Morris ANTISEPTIC Hand Sanitizer (ethyl alcohol 70%), packaged in a) 8.45 fl oz (250 mL) bottles and b) 33.81 fl oz (1L) bottles, Distributed by: Asimex International LLC, 9100 S Dadeland Blvd, Ste 912, Miami, FL 33156, COUNTRY OF ORIGIN: MEXICO.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0795-2021·2021-09-22
Florance Morris Hand Sanitizer Recalled for Methanol Contamination
Florance Morris ANTISEPTIC Hand Sanitizer (70% ethyl alcohol) distributed nationwide is recalled due to FDA-detected methanol contamination and insufficient ethanol content. The product was distributed by Asimex International LLC in Florida.
Product
Florance Morris ANTISEPTIC Hand Sanitizer (ethyl alcohol 70%), packaged in a) 8.45 fl oz (250 mL) bottles and b) 33.81 fl oz (1L) bottles, Distributed by: Asimex International LLC, 9100 S Dadeland Blvd, Ste 912, Miami, FL 33156, COUNTRY OF ORIGIN: MEXICO.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0800-2021·2021-09-22
Lidocaine Hydrochloride Topical Solution Recalled for Superpotency
Teligent Pharma is recalling Lidocaine Hydrochloride Topical Solution, USP 4% due to the product being superpotent. The recall affects 32,544 bottles distributed nationwide in the United States and Canada.
Product
Lidocaine Hydrochloride Topical Solution, USP, 4% , 50 mL glass bottles, Rx Only, Teligent Pharma Inc. Buena, New Jersey 08310, NDC 52565-009-50.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0803-2021·2021-09-22
MIC+Methyl B12 Injection Recalled for Lack of Processing Controls
Promise Pharmacy is recalling MIC+Methyl B12 injection (57 vials, Lot# 06152021@2) distributed across five states due to lack of processing controls that may affect product quality and safety.
Product
MIC+Methyl B12 injection Methionine Inositol Choline+Methylcobalamin 25 mg/50 mg/50 mg/1 mg/mL, 10 mL vial sterile, Rx only, Promise Pharmacy 31818 US Hwy 19N Palm Harbor FL 34684 1-888-3PROMIS
Category
Drug
Distribution
5 states
SevereFDA (Devices)·Z-2429-2021·2021-09-22
Cordis Angiographic Catheter Recall Due to Potential Marker Band Dislodgement
Cordis is recalling approximately 1,610 SUPER TORQUE PIG PIGTAIL SPECIAL angiographic catheters worldwide because the device can become entrapped between endovascular devices and the vessel wall, potentially causing marker band movement or dislodgement.
Product
Cordis 5F SUPER TORQUE PIG PIGTAIL SPECIAL, Angiographic Catheter, REF SRD7040MB
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2431-2021·2021-09-22
Cordis Angiographic Catheter Recalled for Marker Band Dislodgement Risk
Cordis is recalling angiographic catheters that may become entrapped between devices and vessel walls, risking marker band dislodgement during vascular procedures. Approximately 71,330 units were distributed worldwide.
Product
Cordis SUPER TORQUE MB 5F PIG, Angiographic Catheter, REF 532-598B
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2430-2021·2021-09-22
Cordis SUPER TORQUE Angiographic Catheter Recalled for Entrapment Risk
Cordis is recalling the SUPER TORQUE MB angiographic catheter (18,730 units) due to risk of entrapment between endovascular devices and vessel wall, which can cause marker band movement or dislodgement. Units were distributed worldwide.
Product
Cordis SUPER TORQUE MB 5F PIG, Angiographic Catheter, REF 532-598A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0976-2021·2021-09-22
Vita Aid Keto-Elemental Nutrition Powder Recall: Undeclared Milk
Naturo Aid Pharmaceutical Inc. is recalling Vita Aid Keto-Elemental Nutrition (Chocolate) powder due to undeclared milk contamination. The product may pose a risk to consumers with milk allergies.
Product
Vita Aid Keto-Elemental Nutrition (Chocolate), VA-958. The product is a powder, packaged in an aluminum bag , with a net weight of 315g.
Category
Food
Distribution
10 states
HighFDA (Devices)·Z-2444-2021·2021-09-22
Roche cobas infinity software may release incorrect test results to laboratories
Roche Diagnostics is recalling cobas infinity central lab software versions 3.01.03–3.02.08 because under certain circumstances, the software may automatically send false test results to laboratory information systems. Correct results remain available on the instrument.
Product
cobas infinity central lab running software version 3.01.03 through 3.02.08, Catalog#: 07154003001
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2467-2021·2021-09-22
BD SmartSite Needle-Free Connector Valves Recalled for Flow and Occlusion Issues
CAREFUSION is recalling BD SmartSite needle-free connector valves due to difficulty flushing, flow issues, and occlusions that could delay therapy. Approximately 23.8 million units were distributed worldwide.
Product
BD SmartSite, REF: 2000E CHINA; BD SmartSite Connector, REF: 2000E-04; BD SmartSite J-LOOP Extension Set One Needle Free Valve, REF: 20021E7D; BD SmartSite Extension Set One Needle Free Valve Slip Luer, REF: 20037E7D; BD SmartSite Extension Set 3 Needle Free Valves, REF…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2457-2021·2021-09-22
BD Syringe Set Needle-Free Connector Valves May Cause Therapy Delay
BD Syringe Set needle-free connector valves may experience difficulty flushing, flow issues, or occlusions that could delay patient therapy. About 16,700 units have been distributed worldwide.
Product
BD Syringe Set 20 DP MIC TBG 0.2MF CKV Anti-Siphon SmartSite VLV Sensing Disc, REF: 10798696; BD Syringe Set 20 DP MIC TBG CKV Anti-Siphon SmartSite VLV Sensing Disc, REF: 10798703;
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·21199·2021-09-22
Oceanic Adult Dry Top Snorkels Recalled Due to Drowning Hazard
Huish Outdoors is recalling Oceanic Adult Dry Top Snorkels sold at Costco because the bottom purge valve can leak, allowing unexpected water entry that poses a drowning hazard. Consumers should stop using the snorkels immediately.
Product
Oceanic Adult Dry Top Snorkels
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2455-2021·2021-09-22
BD SmartSite Needle-Free Valve Extension Set Recalled for Potential Occlusion
CareFusion recalls BD SmartSite needle-free valve extension sets due to potential occlusion, flow issues, and difficulty flushing that could delay medical therapy.
Product
BD SmartSite 'Y' Extension Set 2 Needle-Free Valves, REF: 20019E7D
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2456-2021·2021-09-22
FDA recalls BD burette sets for connector valve occlusion and flow defects
BD Gravity Burette Sets and Add-On Burette Sets are being recalled due to needle-free connector valve defects that may cause flushing difficulties, flow problems, or complete occlusions, potentially delaying therapy. The recall affects approximately 77,802 units distributed worldwide.
Product
BD Gravity Burette Set 60 DROP 1.2 MF 2 SmartSite VALVES BALL VALVE DRIP CHAMBER V/NV, REF: 10037031; BD Gravity Burette Set 20 DROP 1.2 Micron Filter 2 SmartSite VALVES BALL VALVE DRIP CHAMBER V/NV , REF: 10037032; BD GRAVITY BURETTE SET 60 DROP 2 Smartsite VALVES BALL DRIP…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2465-2021·2021-09-22
BD SE Burette Set needle-free connectors recalled for flow obstruction risk
CareFusion is recalling BD SE Burette Sets with needle-free connector valves that may fail to flush or develop flow obstructions, risking therapy delays. Approximately 56,680 units were distributed worldwide.
Product
BD SE Burette Set 20 Drops 2 Injection Ports Vented/NonVented, REF: 72103E-0006
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2472-2021·2021-09-22
Alinity ci-series System Control Module Software Performance Issues
Abbott's Alinity ci-series analyzers with software version 3.2.3 and earlier have multiple issues that could display expired reagents as valid, fail to alert operators to errors, and produce incorrect test results.
Product
Alinity ci-series System Control Module clinical chemistry and immunoassay analyzer for in vitro diagnostic use. Model number LN 03R70-01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2482-2021·2021-09-22
Braun ThermoScan PRO 6000 Ear Thermometer Recall: Burn Risk from Fluid Exposure
Braun ThermoScan PRO 6000 ear thermometers may overheat if exposed to fluids and used before drying, risking burns to the user or patient. More than 1 million units are affected.
Product
Braun ThermoScan PRO 6000 Ear Thermometer-indicated for the intermittent measurement of human body temperature for patients having ages ranging from normal weight (full term) newborn to geriatric adults in a professional use environment. Model: 6000
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2460-2021·2021-09-22
BD needle-free connector valves recalled for flow obstruction risk
BD needle-free connector valves and extension sets may experience flow obstruction and flushing difficulties, potentially delaying medical therapy. No adverse events have been reported.
Product
BD Extension Set SMALLBORE Tubing SmartSite VALVE, REF: 10010511; BD SmartSite Extension Set Needle-Free Valve, REF: 10010912; BD EXTENSION SET SMALLBORE TUBING DETACHABLE SmartSite VALVE, REF: 10010983; BD Gravity Burette Set 60 DP 4 VersaSafe PORTS 3 SmartSite VALVES BALL…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0978-2021·2021-09-22
Vita Aid SynerClear Powder Recalled for Undeclared Milk Contamination
Naturo Aid Pharmaceutical Inc. is recalling Vita Aid SynerClear (Unflavoured) powder because it may contain undeclared milk residue. Consumers with milk allergies are at risk.
Product
Vita Aid SynerClear (Unflavoured), VA-925. The product is a powder, packaged in a plastic bottle and a white cap, with a net weight of 650g.
Category
Food
Distribution
10 states
HighFDA (Devices)·Z-2443-2021·2021-09-22
Hero Model 100 Smart Pill Dispenser Recalled for Software Dose-Prompting Error
Hero Health is recalling the Model 100 smart pill dispenser due to a software defect causing the device to prompt users to take medication doses that have already been dispensed, creating overdose risk.
Product
The Hero Model 100 (H-100) is a system consisting of a smart pill dispenser and a medication management app.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2476-2021·2021-09-22
Philips Azurion Imaging System Failure at 480V Hospital Power Supply
Philips Azurion medical imaging devices may fail when powered by hospital electrical systems providing 480V. The failure reduces X-ray performance and may be preceded by a burning smell.
Product
The Azurion series (within the limits of the used Operation Room table) are intended for use to perform: "Image guidance in diagnostic, interventional and minimally invasive surgery procedures for the following clinical application areas: vascular, non-vascular, cardiovascular…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0977-2021·2021-09-22
Vita Aid Keto-Elemental Nutrition powder recalled for undeclared milk
Naturo Aid Pharmaceutical is recalling Vita Aid Keto-Elemental Nutrition (Thai) powder because it may contain undeclared milk residue. The product was distributed across ten U.S. states.
Product
Vita Aid Keto-Elemental Nutrition (Thai), VA-958. The product is a powder, packaged in an aluminum bag , with a net weight of 315g.
Category
Food
Distribution
10 states
HighFDA (Devices)·Z-2479-2021·2021-09-22
Bariatric ceiling-mounted lift spreader bar can disconnect from scale attachment
Arjohuntleigh recalls 62 Maxi Sky 1000 and V10 bariatric ceiling lifts because the spreader bar can disconnect from the scale attachment. Users should immediately stop using affected units and contact the manufacturer.
Product
Maxi Sky 1000 (Arjo) and V10 (BHM) Bariatric Ceiling Rail - Mounted Lift with measuring function
Category
Medical Device
Distribution
11 states
HighFDA (Devices)·Z-2470-2021·2021-09-22
Arjo Disposable Repositioning Sling Recalled for Trip Hazard Risk
Getinge recalled 46,085 Arjo Disposable Repositioning Sling units because the sling loop straps pose a trip hazard. The affected devices were distributed nationwide to healthcare facilities.
Product
Arjo Disposable Repositioning Sling, Model AHD001
Category
Medical Device
Distribution
Distributed nationwide