State

Arizona product recalls

73,376 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 73,376 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

20651–20675 of 81763

SevereFDA (Food)·F-1660-2022·2022-09-07
Lyons Barista Frappe Base recalled for bacterial contamination
Lyons Magnus is recalling Barista Style Sweet Cream Frappe Base nationwide due to findings of and potential for Cronobacter sakazakii and Clostridium botulinum.
Product
Lyons Barista Style Sweet Cream Frappe Base 32 fl oz (1qt) 946 mL. UPC 0 45796-10089 3. Shake well before using. After opening, keep refrigerated and use within 7 days. 4count Case UPC 629046564019.
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1676-2022·2022-09-07
Oatly Oat Drink Recalled for Bacterial Contamination Findings
Oatly Oat Drink Deluxe 330ml is being recalled for findings of Cronobacter sakazakii and Clostridium botulinum. Approximately 53.8 million units nationwide are affected. Consumers should not consume the product.
Product
PROUCT WAS NOT DISTRIBUTED IN US. The Original Oatly! Oat Drink Deluxe 330ml. UPC 7 394376 619021 18 count case UPC 27394376619025. Shake well before drinking. Produced in the USA. Oatly AB, Stora Varvsgatan 6a, SE-211 19 Malmo.
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1617-2022·2022-09-07
Lyons Barista Oat Beverage Recalled for Potential Bacterial Contamination
Lyons Magnus is recalling Lyons Barista Style Oat, a plant-based milk beverage distributed nationwide, due to potential contamination with Cronobacter sakazakii and Clostridium botulinum.
Product
Lyons Barista Style Oat, Non-Dairy Beverage. Plant-Based Milk. 32 FL OZ (1 QT) 946mL UPC 0 45796-10180 7. 12 count case UPC 10045796101804. Shake Well before Serving. After opening keep refrigerated and use within 7 days. Lyons Magnus, Fresno, CA 93702.
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1675-2022·2022-09-07
Oatly Oat-Milk Recalled for Potential Cronobacter and Botulinum Contamination
Oatly Original Oat-Milk is being recalled nationwide due to potential findings of Cronobacter sakazakii and Clostridium botulinum contamination. Approximately 53.8 million units are affected.
Product
The Original Oatly! Oat-Milk 11 fl oz (330ml). UPC 1 90646-63013 3. 18 count case UPC 20190646630137. Distributed by Oatly Inc., 220 E 42ndSt., Ste. 409A, New York, NY 10017.
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1647-2022·2022-09-07
Plant-based protein shake recalled for Cronobacter and botulinum contamination
Lyons Magnus is recalling nationwide its Lyons Ready Care Plant-Based Protein Shake due to findings of and potential for Cronobacter sakazakii and Clostridium botulinum contamination. Affected lot codes are 5221 (08/08/2022) and 6221 (08/09/2022).
Product
Lyons Ready Care Plant-Based Protein Shake Vanilla. 8.45 fl oz. ( 250mL)UPC 0 45796-10080 0. Mildly Thick Nectar Consistency. Refrigerate prior to serving. Shake well. Sold in 24-count case UPC 10045796100807. Lyons Magnus, Fresno, CA 93702.
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1521-2022·2022-09-07
NIM EMG Endotracheal Tubes recalled for risk of airway obstruction
Medtronic Xomed is recalling NIM EMG Endotracheal Tubes due to reports of airway obstruction during use. The recall affects 23,820 units distributed worldwide.
Product
NIM EMG Endotracheal Tube, Part Numbers: a) REF 8229307J b) REF 8229308J c) REF 8229306J
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1664-2022·2022-09-07
Abbott PediaSure Harvest infant nutrition recalled for bacterial contamination
Abbott PediaSure Harvest 1.0 Cal formula is being recalled nationwide due to potential contamination with Cronobacter sakazakii and Clostridium botulinum bacteria.
Product
Abbott PediaSure Harvest 1.0 Cal, For Tube Feeding. Complete nutrition blend. 8 fl oz (237mL). UPC 0 70074-67963 1. 24 count case UPC 00070074679624. Shake very well. Store unopened at room temperature. Once opened, reclose, refrigerate, and use within 24 hours.…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1672-2022·2022-09-07
Kate Farms Pediatric Peptide Formula Recalled for Bacterial Contamination
Lyons Magnus is recalling kate farms Pediatric Peptide formula nationwide due to potential Cronobacter sakazakii and Clostridium botulinum contamination. The recall affects 53.8 million units of this ready-to-use pediatric nutrition formula.
Product
kate farms Pediatric Peptide 1.5 Cal/mL, Vanilla, Sole-Source Nutrition Formula. 250 mL (8.45 fl oz) UPC 8 51823-00687 4. 12 count case UPC 00851823006201. Shake Well. A ready-to-use oral and tube feeding formula with enzymatically hydrolyzed organic pea protein. Made for…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1657-2022·2022-09-07
Sated Complete Keto Meal Shake Chocolate recalled for potential bacterial contamination
Lyons Magnus, Inc. recalls Sated Complete Keto Meal Shake Chocolate Flavor due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. More than 53 million units distributed nationwide.
Product
Sated Complete Keto Meal Shake Chocolate Flavor. 11 fl oz (325ml) UPC 8 57227-00721 9. 12 Count Case UPC 00857227007219. Distributed by LongRun LLC, Belmont, MA 02478. Important: Must be refrigerated after opening to maintain safety.
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1649-2022·2022-09-07
Cafe Grumpy Cold Brew Coffee Recalled for Potential Bacterial Contamination
Lyons Magnus is recalling Cafe Grumpy Ready to Drink Cold Brew Coffee nationwide due to findings of and potential for Cronobacter sakazakii and Clostridium botulinum. Affected lots have best-by dates of 08/27/2022 or 08/28/2022.
Product
Cafe Grumpy Ready to Drink Cold Brew Coffee 11 fl oz. UPC 7 58524-05908 9. Sold in 4-count case UPC 00758524059003. Refrigerate after opening. Shake before opening. Cafe Grumpy Beverage Company, 199 DiamondSt., Brooklyn, NY 11222
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1656-2022·2022-09-07
Organic Valley Organic Whole Milk recalled for potential Cronobacter and botulinum contamination
Lyons Magnus is recalling approximately 53.8 million units of Organic Valley Organic Whole Milk nationwide due to potential contamination with Cronobacter sakazakii and Clostridium botulinum.
Product
Organic Valley Organic Whole Milk. 8 fl oz UPC 0 93966-00818 0. 12 Count Case UPC 00093966008531.
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1606-2022·2022-09-07
Aloha Organic Protein Drink recalled nationwide for potential bacterial contamination
Lyons Magnus is recalling 53.8 million units of Aloha Organic Protein Drink iced coffee variety nationwide due to potential contamination with Cronobacter sakazakii and Clostridium botulinum.
Product
Aloha Organic Protein Drink, Iced Coffee Plant-based protein. Net 11 FL OZ (330 mL) Tetra Pak container UPC 8 42096-11238 6. Sold as 4 count package wrap with UPC 842096122385. Shake Well. Best Chilled. Manufactured for: Aloha, Littleton, CO 80127
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1661-2022·2022-09-07
Whey Protein Drink Recalled Nationwide for Potential Bacterial Contamination
Optimum Nutrition Gold Standard 100% Whey Vanilla is being recalled nationwide due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. Affected product has lot code 2321 with best-by date 08/20/2022.
Product
Optimum Nutrition Gold Standard 100% Whey Vanilla 11 fl oz (325mL). UPC 7 48927-06410 0. Shake well. Best when served chilled. Manufactured for Optimum Nutrition, Inc., 3500 Lacey Road, Suite 1200, Downers Grove, IL 60515
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1609-2022·2022-09-07
Pediatric Nutrition Formula Recalled for Potential Bacterial Contamination
Kate Farms Pediatric Standard Sole-Source Nutrition Formula is recalled nationwide due to findings of potential Cronobacter sakazakii and Clostridium botulinum contamination.
Product
kate farms Pediatric Standard Sole-Source Nutrition Formula. 1.2 cal/mL. 250 ML (8.45 FL OZ) Tetra Pak container UPC 8 51823-00690 4. Sold in 12 count case UPC 00851823006997. Refrigerate after opening. Made for: Kate Farms, Inc., 101 innovation Place, Santa Barbara…
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1649-2022·2022-09-07
Metalogix Self-Drill Half-Pin Surgical Component Recalled for Tip Breakage
New Standard Device Inc is recalling Metalogix Self-Drill Half-Pins used in external fixation surgery due to reports of tip breakages occurring during surgical procedures.
Product
Metalogix Self-Drill Half-Pin, a component of the Revolution External Fixation System. Orthopedic. Metalogix Self-Drill Half-Pin 5x30x215mm REF 620030 Metalogix Self-Drill Half-Pin 5x40x215mm REF 620040 Metalogix Self-Drill Half-Pin 5x60x215mm REF 620060…
Category
Medical Device
Distribution
11 states
HighFDA (Devices)·Z-1660-2022·2022-09-07
ARCHITECT STAT Troponin-I Reagent Kit Recalled for Insufficient Blocking Agents
Abbott is recalling one lot of ARCHITECT STAT Troponin-I Reagent Kits due to insufficient heterophilic blocking agents in the conjugate, which may affect test accuracy.
Product
ARCHITECT STAT Troponin-I Reagent Kit, REF 2K41-27
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1682-2022·2022-09-07
Sweetums Sucrose Solution Recalled for Contamination and Leaking Cups
Clinical Innovations is recalling Sweetums 24% Sucrose Solution used in NICU settings due to leaking cups and black particulates in the solution. The recall affects 1,773 boxes distributed nationwide.
Product
Sweetums 24% Sucrose Solution Preservative Free 15 mL cups VPSU15037288. Each box contains 288 cups. Product is aseptically packaged in 15 mL cups with foil lid. Each cup contains 15 mL of USP purified water, 24% sugar, citric acid (buffer). Cup is latex-free, DEHP-free…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1647-2022·2022-09-07
Siemens Artis icono X-Ray Systems Recalled for Potential Hardware Failure
Siemens has recalled Artis icono X-ray imaging systems due to a potential hardware issue affecting a specific lot of X-ray tubes. If the error detection mechanism fails, the system cannot release X-rays until it is shut down.
Product
Artis icono biplane- Model No. 11327600 Artis icono floor- Model No. 11327700
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1648-2022·2022-09-07
Siemens Dimension Vista CA 15-3 Diagnostic Cartridges Recalled for Measurement Bias
Siemens Healthcare Diagnostics is recalling Dimension Vista CA 15-3 Flex reagent cartridges because the diagnostic test can produce inaccurate results, reading 26–33% lower than actual values, potentially delaying appropriate patient treatment decisions.
Product
Dimension Vista LOCI CA 15-3 Flex reagent cartridge. In Vitro Diagnostic for the quantitative measurement of CA 15-3. Siemens Material Number (SMN)/Ref Catalog Number : 10464344/K6456
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1673-2022·2022-09-07
Eye imaging device software defect affects surgical planning calculations
Pentacam eye imaging devices with certain software versions have a bug that causes inaccurate surgical planning printouts for toric intraocular lens procedures.
Product
Pentacam AXL REF 70100, Pentacam HR REF 70900. Used to image the anterior segment of the eye.
Category
Medical Device
Distribution
37 states
HighFDA (Devices)·Z-1666-2022·2022-09-07
Radiographic imaging system may exceed radiation dose limits in biplane mode
Canon Medical's Alphenix i imaging systems may deliver radiation dose rates exceeding acceptable limits during biplane fluoroscopic procedures. Sixteen systems nationwide with software versions 8.0, 9.0, or 9.2 and TFP 1200C detector are affected.
Product
INFX-8000V. For radiographic and fluoroscopic studies and intervention.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V671000·2022-09-07
Nissan Titan vehicles recalled for transmission parking pawl failure risk
Nissan is recalling 2020-2023 Titan vehicles and certain other models because the transmission parking pawl may fail to engage in park, risking vehicle rollaway and crash.
Product
NISSAN — NISSAN TITAN, FRONTIER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-1581-2022·2022-09-07
Arborio Rice Recalled for Possible Glass Contamination
Multiple Arborio rice products are being recalled by Woodland Foods LLC due to possible presence of glass pieces. Consumers should not use the affected products.
Product
Woodland Ingredients X06D Arborio Rice, 25 lbs. bag UPC 00687080007374 Woodland Ingredients X16D Italian Arborio Rice, 25 lbs. bag UPC 00687080069143 Sysco International X06D05 Arborio Rice, 25 lbs. bag in box UPC 00074865718257 DGourmet.com X06C Arborio Rice, 10 lbs. bag in…
Category
Food
Distribution
23 states
HighFDA (Food)·F-1684-2022·2022-09-07
Clinical Innovations Sweetums Sucrose Solution Vials Recalled for Contamination
Clinical Innovations is recalling Sweetums 24% sucrose solution vials due to complaints of leaking, black liquid, and black particulates in product vials. The recall affects neonatal products distributed nationwide and internationally.
Product
Sweetums 24% sucrose solution preservative free. Vials containing 1ml or 2ml of 24% sucrose in purified water. Product is administered by drop using vials and tip allows controlled administration directly to tongue or buccal surface. Product is only used in the hospital…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1645-2022·2022-09-07
X-Ray Imaging System X-Ray Tube Hardware Defect Worldwide Recall
Siemens has recalled Artis Q and Artis Q.zen X-ray imaging systems due to a potential X-ray tube hardware defect. In rare cases, if error detection fails, the system will not be able to release X-ray until shut down; 1,389 units are affected globally.
Product
Artis Q floor- Model No. 10848280 Artis Q ceiling- Model No. 10848281 Artis Q biplane- Model No. 10848282 Artis Q zeego- Model No. 10848283 Artis Q.zen floor- Model No. 10848353 Artis Q.zen ceiling- Model No. 10848354 Artis Q.zen biplane- Model No. 10848355
Category
Medical Device
Distribution
Distributed nationwide