Product Recalls in Arkansas
Product recalls affecting Arkansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Arkansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,591 recalls have been distributed to Arkansas in the last 12 months.
Showing 15081–15100 of 49,990 recalls
Recalled Item: JUST Egg Inspired by India Curry Recalled by Cuisine Solutions Due to...
The Issue: Undeclared egg and milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: JUST Egg Inspired by Mexico Roasted Poblanos Recalled by Cuisine Solutions...
The Issue: Undeclared egg and milk
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Covidien HysteroLux Fluid Management System Control Unit Recalled by WOM...
The Issue: When the display of inflow volume to the uterus reaches 32450 ml, the fluid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThermoScientific Oxoid Antimicrobial Susceptibility Discs Rx only Made in...
The Issue: Out of Specification
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Plus Ventilator with Software Versions 3.00 and...
The Issue: It has been identified that ventilators equipped with High Flow Therapy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Ventilator with Software Versions 3.00 and 3.10....
The Issue: It has been identified that ventilators equipped with High Flow Therapy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tight! Xtreme Reloaded: 120 count capsules (serving size 3 capsules)...
The Issue: FDA inspection found New Dietary Ingredient, Hordenine, in the supplement...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Hemotherm CE Dual Reservoir Cooler/Heater Recalled by Gentherm Medical, LLC...
The Issue: There is a potential risk of device contamination and patient infection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acetaminophen 325 mg tablets Recalled by Spirit Pharmaceuticals Due to cGMP...
The Issue: cGMP deviations: Discolored acetaminophen
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Argyle UVC Insertion Tray containing Safety Scalpel N11 (vendor part...
The Issue: The current Argyle UVC Insertion Tray does not include a specific IFU to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hatch Verde Salsa Medium Net Wt. 12 oz (340g) 6 Recalled by Heritage Family...
The Issue: Potential to contain a foreign material
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: E6164J2 Taco Casa Green Salsa 8 x 4 lb (1.8 kg) pouches Recalled by Heritage...
The Issue: Potential to contain a foreign material
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Proteus 235- designed to produce and deliver a proton beam Recalled by Ion...
The Issue: Users may be misled by the popup message displayed by the Proton Therapy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Suture Anchor Recalled by Arthrex, Inc. Due to Not properly sterilized,...
The Issue: Not properly sterilized, because the outer pouch seal on the Tyvek header...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy 100 Recalled by Philips Respironics, Inc. Due to The polyester-based...
The Issue: The polyester-based polyurethane (PE-PUR) foam may degrade into particles...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A-Series BiPAP A 40 Recalled by Philips Respironics, Inc. Due to The...
The Issue: The polyester-based polyurethane (PE-PUR) foam may degrade into particles...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A-Series BiPAP Hybrid A30 (not marketed in US) Recalled by Philips...
The Issue: The polyester-based polyurethane (PE-PUR) foam may degrade into particles...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoreValve Evolut PRO Delivery Catheter System Recalled by Medtronic Heart...
The Issue: Due to reports of actuator separation for various delivery catheter systems....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoreValve Evolut R Delivery Catheter System Recalled by Medtronic Heart...
The Issue: Due to reports of actuator separation for various delivery catheter systems....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoreValve Evolut PRO PLUS Delivery Catheter System Recalled by Medtronic...
The Issue: Due to reports of actuator separation for various delivery catheter systems....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.