Product Recalls in Arizona
Product recalls affecting Arizona — including food, drugs, consumer products, medical devices, and vehicles distributed to Arizona. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,160 recalls have been distributed to Arizona in the last 12 months.
Showing 1921–1940 of 52,339 recalls
Recalled Item: PeriGiene Recalled by DermaRite Industries, LLC Due to Microbial...
The Issue: Microbial Contamination of Non-Sterile Drug Product: The products were found...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TOPS Inserter Recalled by PREMIA SPINE LTD Due to Potential for missing pins...
The Issue: Potential for missing pins at tip of inserter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentax Medical Video Processor Recalled by Pentax of America Inc Due to...
The Issue: During endoscopic procedures using a combination of the video processor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Queen Bee Gardens Whipped Honey Pure. Intended use: Recalled by...
The Issue: Product may have small flakes of stainless steel in product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Brand Name: Queen Bee Gardens Whipped Honey Raspberry. Intended use:...
The Issue: Product may have small flakes of stainless steel in product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Brand Name: Queen Bee Gardens Whipped Honey Huckleberry Intended use:...
The Issue: Product may have small flakes of stainless steel in product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above safety...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chromophare Surgical Light System Recalled by Stryker Communications Due to...
The Issue: Surgical lights have stress lines forming on the powder coating, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plastic Trial Head Brown Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...
The Issue: Inconsistent size terminology and color coding used on labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prosthesis Head B Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to...
The Issue: Inconsistent size terminology and color coding used on labeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin Operating Tables Model Numbers: (1) 770001A0 Recalled by MAQUET GMBH...
The Issue: Under certain conditions, such as the simultaneous use of the operating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline ReNewal Reprocessed St. Jude Medical Response and Supreme Diagnostic...
The Issue: Specific lots of reprocessed electrophysiology catheters may contain small...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3mensio Workstation (Vascular Fenestrated) software Recalled by PIE Medical...
The Issue: When fenestrated analysis with clock measurements is started in diagnostic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dubai emek SPREAD PISTACHIO CACAO CREAM WITH KADAYIF NET WT. Recalled by...
The Issue: Salmonella. The firm was notified by the FDA that the product may be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Baxter Novum IQ Large Volume Pump Recalled by Baxter Healthcare Corporation...
The Issue: Baxter is issuing an Urgent Medical Device Correction for the Novum IQ large...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectrum IQ Infusion Pump Recalled by Baxter Healthcare Corporation Due to...
The Issue: Baxter has identified that certain pumps have potentially been released with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Organic Pure Stevia Recalled by NuNaturals Inc Due to Product is Monk Fruit...
The Issue: Product is Monk Fruit powder but bottle was mis-labeled as Organic Pure Stevia.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pure Monk Fruit Sweetener Recalled by NuNaturals Inc Due to Product is...
The Issue: Product is Stevia powder but bottle was mis-labeled as Pure Monk Fruit...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sucralfate Tablets Recalled by Nostrum Laboratories, Inc. Due to CGMP...
The Issue: CGMP Deviations: The recalling firm filed for Chapter 11 in September 2024....
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ELEOS SEGMENTAL LIMB SALVAGE SYSTEM Recalled by Onkos Surgical, Inc. Due to...
The Issue: Unidentified substance of unknown impact was identified on devices during a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.