State

Arizona product recalls

73,106 recalls have nationwide distribution and so reach Arizona. 8,386 additional recalls listed Arizona specifically in their distribution scope.

What the numbers show

Total: 8,386
Critical: 1,313
Severe: 1,720
Most recent: 2026-10-02

Of the 8,386 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 1,720 (21%) are Severe.

Which agencies issued them

These figures cover only the 8,386 recalls whose distribution notice names Arizona specifically. The 73,106 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

12801–12825 of 81492

HighFDA (Drugs)·D-0400-2024·2024-04-03
Fentanyl and Bupivacaine Epidural Injection Recalled for Sterility Assurance Issue
SCA Pharmaceuticals recalls 412 cassettes of fentanyl-bupivacaine epidural injection (lots 1223049261 and 1223049724) due to lack of assurance of sterility.
Product
fentaNYL 500 mcg/100 mL, Bupivacaine HCl 0.04% in 0.9% Sodium Chloride 100 mL Injection (fentaNYL Concentration = 5 mcg/mL), EPIDURAL USE ONLY, 100 mL Yellow CADD Cassette, Rx only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095, NDC 70004-0289-64, Bar Code 70004028964
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1098-2024·2024-04-03
Barsotti Organic Carrot Juice recalled due to under-processing
Barsotti Organic Carrot Juice in 16 oz and 64 oz bottles (also sold under Trader Joe's label) is recalled because it was determined to be under-processed. This may allow harmful bacteria to survive.
Product
Barsotti Organic Carrot Juice 16 oz. and 64 oz. plastic bottles Perishable, Keep Refrigerated Ingredient: Fresh Pressed Organic Carrot Juice. Flash Pasteurized. Barsotti Juice Co., Camino, CA 95709 (530_ 622-4629 www.barsottijuice.com Trader Joe's 100% Juice Organic Carrot…
Category
Food
Distribution
10 states
HighFDA (Devices)·Z-1391-2024·2024-04-03
Puritan HydroFlock Collection Device Distributed with Wrong Product Code
Puritan Medical Products distributed HydroFlock Sterile Flocked Collection Devices labeled as Part Number 25-3317-H, Lot S1014 that actually contain product code 25-3317-U. Approximately 232,500 units were affected.
Product
HydroFlock Sterile Flocked Collection Device, Part Number 25-3317-H.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1366-2024·2024-04-03
MediBeads Neck Wrap recalled for potential mold and mildew growth
Bruder Healthcare Company is recalling 430 units of MediBeads Neck Wrap (Item 34320) because the product may have been exposed to excessive moisture, creating potential for mold and mildew growth. Lot Number M053300, distributed in the US and Canada.
Product
MediBeads Neck Wrap, Item Number 34320
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1094-2024·2024-04-03
Himalayan Pain Relief Tea Contains Undeclared Pharmaceutical Drugs
WS Global Inc is recalling Himalayan Pain Relief Tea nationwide due to undeclared pharmaceutical drugs—Diclofenac and Dexamethasone Acetate—that were not listed on the product label.
Product
Himalayan Pain Relief Tea for Gout and Hangover
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1361-2024·2024-04-03
Thermalon Sinus Compress Recalled for Potential Mold and Mildew
Bruder Healthcare Company is recalling 1,416 units of Thermalon Sinus Compress (Item Number 24332) due to potential mold and mildew growth from excessive moisture exposure. Affected lot numbers are M053160 and M053570.
Product
Thermalon Sinus Compress, Item Number 24332
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1390-2024·2024-04-03
Boston Scientific iSLEEVE Expandable Introducer Sets Recalled for Hemostatic Valve Leak
Boston Scientific is recalling specific batches of the iSLEEVE Expandable Introducer Set due to hemostatic valve leaks affecting 4,060 devices. The devices are distributed in the US, Canada, and worldwide.
Product
Boston Scientific iSLEEVE EXPANDABLE Introducer Set REF H74939349140, facilitates femoral access to the vascular system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0419-2024·2024-04-03
Pharmaceutical Injection Recalled Due to Lack of Sterility Assurance
SCA Pharmaceuticals is recalling PHENYLephrine HCl 40 mg injection nationwide due to lack of sterility assurance. Patients should contact their healthcare provider and not use this product.
Product
PHENYLephrine HCl 40 mg in 0.9% Sodium Chloride Injection, (Concentration = 160 mcg/mL), 250 mL Bag, Rx Only, SCA Pharmaceuticals, 755 Rainbow Rd. Windsor, CT 06095, NDC 70004-0825-40, Bar Code 70004082540.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1369-2024·2024-04-03
Cystatin C Calibrator Series CVS 2699 Recalled for Calibration Bias
Randox Laboratories is recalling Cystatin C Calibrator Series CVS 2699 because it runs with negative bias compared to other methods, which could affect test accuracy on automated analyzers.
Product
Cystatin C Calibrator - In vitro diagnostic (IVD) use in the calibration of the Randox Cystatin C assay on automated analysers Catalog Number: CVS 2699
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·24V247000·2024-04-03
Winnebago Recalls 2024 Access Trailers Due to GFCI Wiring Defect
Winnebago is recalling 2024 Access travel trailers because incorrectly wired GFCI outlets may lack protection, increasing the risk of electrical shock.
Product
WINNEBAGO — WINNEBAGO ACCESS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24E031000·2024-04-03
Watson & Chalin Recalls SL2065 Steerable Lift Axle Suspension Systems
Watson & Chalin is recalling SL2065 steerable lift axle suspension systems because bearing journals may not be fully seated, creating a risk of spindle fracture and crash.
Product
STEERING:LINKAGES:KNUCKLE:SPINDLE:ARM recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1360-2024·2024-04-03
Thermalon Sinus Compress Recalled for Potential Mold and Mildew Growth
Bruder Healthcare Company is recalling certain lots of Thermalon Sinus Compress due to potential mold and mildew growth from moisture exposure. The product was distributed in the US and Canada.
Product
Thermalon Sinus Compress (French), Item Number 24332F
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0420-2024·2024-04-03
PHENYLephrine HCl Injectable Recalled Due to Lack of Sterility Assurance
SCA Pharmaceuticals is recalling PHENYLephrine HCl 800 mcg/10 mL injections due to lack of assurance of sterility. The recall affects 3,671 syringes distributed nationwide.
Product
PHENYLephrine HCl 800 mcg/10 mL in 0.9% Sodium Chloride Injection, (Concentration = 80mcg/mL) 10 mL fill 12 mL Syringe, Rx Only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095, NDC 70004-0816-12, Bar Code 700040081612.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1372-2024·2024-04-03
Laboratory performance verifier recalled for mismatched diluent assembly
Ortho-Clinical Diagnostics is recalling 10,911 units of VITROS Performance Verifier I worldwide due to mismatched diluent components that could cause inaccurate quality control test results.
Product
VITROS Performance Verifier I
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0407-2024·2024-04-03
Hydromorphone Injection Recalled Due to Lack of Sterility Assurance
SCA Pharmaceuticals recalls 1,023 syringes of Hydromorphone Injection nationwide due to lack of sterility assurance. No illnesses have been reported.
Product
HYDROmorphone HCl 10 mg/50 mL in 0.9% Sodium Chloride Injection (Concentration = 0.2 mg/ml) 50 mL fill Syringe, Rx only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095, NDC 70004-0300-22, Bar Code 70004030022
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0424-2024·2024-04-03
Succinylcholine Chloride Injection Recalled for Sterility Assurance Failure
SCA Pharmaceuticals is recalling 5,079 syringes of Succinylcholine Chloride Injection nationwide due to lack of sterility assurance. Affected lots are #1223049085 and #1223049364.
Product
SUCcinylcholine Chloride 100 mg/5mL Injection (Concentration = 20mg/mL), 5 mL fill 6 mL Syringe, Rx only, Repackaged by SCA Pharma, 755 Rainbow Rd., Windsor, CT 06095, NDC 70004-0908-09, Bar Code 70004090809
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1364-2024·2024-04-03
Thermalon Heating Pads Recalled for Potential Mold and Mildew Growth
Bruder Healthcare recalls Thermalon Heating Pad model 24002 due to potential mold and mildew growth from moisture exposure. Affected units were distributed nationwide in the US and to Canada.
Product
Thermalon Heating Pad, Item Number 24002
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1386-2024·2024-04-03
Philips Patient Information Center Custom Ringtones Fail When Screen Locked
Philips Patient Information Center iX running software version 4.X may not play custom ringtones when iOS screens are locked with a passcode. Approximately 257,183 units have been distributed worldwide. No injuries have been reported.
Product
Patient Information Center iX (PIC iX), Model Numbers 866389, 866390 (PIC iX Expand), and 866424 (PIC iX Hardware) running Software Version Number 4.X
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1363-2024·2024-04-03
Thermalon Neck Wrap recalled due to potential mold and mildew growth
Bruder Healthcare Company is recalling Thermalon Neck Wrap (Item Number 24322) from certain lots due to potential mold and mildew growth from excessive moisture exposure. Consumers should discontinue use and contact the manufacturer.
Product
Thermalon Neck Wrap, Item Number 24322
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1387-2024·2024-04-03
CareEvent Event Management System notification failure on locked iOS devices
The CareEvent Event Management System's Care Assist mobile application fails to play custom ringtones when iOS device screens are locked with a passcode. This may result in missed alerts or notifications.
Product
CareEvent Event Management System, Model Numbers 866435 and 866436 (CareEvent Upgrade), Software Version Number C.03.X
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0427-2024·2024-04-03
FDA Recalls VCF Contraceptive Film Due to Manufacturing Process Violations
The FDA is recalling VCF Contraceptive Film due to manufacturing process deviations. Apothecus Pharmaceutical Corp. initiated the voluntary recall on March 21, 2024, affecting 17,280 cartons distributed nationwide.
Product
VCF CONTRACEPTIVE — VCF CONTRACEPTIVE (NONOXYNOL-9)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1376-2024·2024-04-03
Access Substrate Reagent Bottles Recalled for Missing Product Labels
Beckman Coulter is recalling Access Substrate reagent bottles (REF 81906) due to missing product labels on certain manufacturing lots. While the missing labels may delay patient test result reporting, no incorrect results have been reported.
Product
Access Substrate, REF 81906, For use with the Access Immunoassay Systems
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·24V245000·2024-04-02
2021 Jayco Redhawk motorhomes recalled for power steering connection defect
Certain 2021 Jayco Redhawk motorhomes have a defective power steering connection that can cause sudden loss of power steering and brake assist, increasing crash risk. Dealers will replace the defective parts free of charge.
Product
JAYCO — JAYCO, ENTEGRA GREYHAWK, ESTEEM, ODYSSEY, GREYHAWK PRESTIGE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V246000·2024-04-02
2024 Hyundai Santa Fe rearview camera obstruction recall
The rearview camera image may be obstructed by a trailer parking assist message, reducing rearward visibility and increasing crash risk. An over-the-air software update will fix the issue.
Product
HYUNDAI — HYUNDAI SANTA FE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V244000·2024-04-01
2023 Kia Forte: Front Suspension Control Arm Failure Risk
Kia recalls certain 2023 Forte vehicles because the right front lower control arm may be improperly welded and fail, risking sudden loss of steering control and crashes.
Product
KIA — KIA FORTE
Category
Vehicle
Distribution
Distributed nationwide