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. 2,732 recalls have been distributed to Arizona in the last 12 months.
Showing 9541–9560 of 52,339 recalls
Recalled Item: Safe tussin PM Recalled by Denison Pharmaceuticals, LLC Due to CGMP...
The Issue: CGMP Deviations: Use of non-food grade lubricant in mixing vessel.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Colic Calm Recalled by Denison Pharmaceuticals, LLC Due to CGMP Deviations:...
The Issue: CGMP Deviations: Use of non-food grade lubricant in mixing vessel.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pin-Away PYRENTAL PAMOATE (Pyrantel base 50 mg / mL) Pinworm Treatment...
The Issue: CGMP Deviations: Use of non-food grade lubricant in mixing vessel.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gose con Sandia Recalled by Avery Brewing Company Due to Due to over...
The Issue: Due to over pressurization, can may fail/explode.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: V-Sign Sensor 2 Recalled by SenTec AG Due to The sensors may experience an...
The Issue: The sensors may experience an out-of-box failure because after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sertera 14 Gauge Biopsy Device-intended to obtain percutaneous core biopsy...
The Issue: The inner needle of the Sertera device is either detaching or discharging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGACY SMARTBASE Recalled by Implant Direct Sybron Manufacturing LLC Due to...
The Issue: Non-engaging abutments were distributed without FDA clearance; the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith&Nephew ENGAGE Cementless Partial Knee System Recalled by Smith &...
The Issue: Recent complaint data indicates that the revision rate may be trending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith&Nephew ENGAGE Cementless Partial Knee System Recalled by Smith &...
The Issue: Recent complaint data indicates that the revision rate may be trending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith&Nephew ENGAGE Cementless Partial Knee System Recalled by Smith &...
The Issue: Recent complaint data indicates that the revision rate may be trending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith&Nephew ENGAGE Cementless Partial Knee System Recalled by Smith &...
The Issue: Recent complaint data indicates that the revision rate may be trending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Famotidine Tablets Recalled by Glenmark Therapeutics, Inc. Due to Labeling:...
The Issue: Labeling: Label Error on Declared Strength: some cartons labeled and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Top Label: TRADER JOE'S GENOVA PESTO NET WT. 7 OZ. Recalled by Bakkavor...
The Issue: The firm was notified that the product top label reads "Pesto" and the side...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Trilogy Evo Recalled by Philips Respironics, Inc. Due to Environmental...
The Issue: Environmental debris may accumulate on the internal machine flow sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo O2 and LifeVent EVO2 Recalled by Philips Respironics, Inc. Due...
The Issue: Environmental debris may accumulate on the internal machine flow sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Veritor System for Rapid Detection of SARS-CoV-2 & Flu A+B Recalled by...
The Issue: IFU- Instructions for Use (IFU) package insert and both the IFU packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo O2 EV300 Recalled by Philips Respironics, Inc. Due to...
The Issue: Environmental debris may accumulate on the internal machine flow sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo Universal Ventilator Recalled by Philips Respironics, Inc. Due...
The Issue: The Trilogy Evo Universal ventilator provides continuous or intermittent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QIAstat-Dx Respiratory SARS-CoV-2 Panel multiplexed nucleic acid real-time...
The Issue: Faulty cartridges in the lot could result in false test results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neonatal TPN Starter Bag Recalled by Central Admixture Pharmacy Services,...
The Issue: Lack of Assurance of Sterility: after an FDA inspection called into question...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.