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. 2,755 recalls have been distributed to Arizona in the last 12 months.
Showing 8421–8440 of 29,154 recalls
Recalled Item: EXALT Model D Single- Use Duodenoscope (Box 1) UPN: M00542420 Recalled by...
The Issue: Updated Instructions for Use (IFU) for EXALT Model D Single-Use Duodenoscope...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXALT Model D Single- Use Duodenoscope (Box 2) UPN: M00542421 Recalled by...
The Issue: Updated Instructions for Use (IFU) for EXALT Model D Single-Use Duodenoscope...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: First Aid Kits containing acetaminophen under brand names Equate (Walmart)...
The Issue: Kits contained recalled acetaminophen.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Harmony Delivery Catheter System. Part of the Harmony Transcatheter...
The Issue: There is potential for the capsule bond to break during the procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FORE-SIGHT ELITE Tissue Oximeter module Recalled by Edwards Lifesciences,...
The Issue: The StO2 values may be inaccurately low when using either the FORE-SIGHT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FORE-SIGHT ELITE Absolute Tissue Oximeter Recalled by Edwards Lifesciences,...
The Issue: The StO2 values may be inaccurately low when using either the FORE-SIGHT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AccessPLUS Large Bore Hemostasis Valves Recalled by Merit Medical Systems,...
The Issue: A design change made to a hemostasis valve to improve manufacturability...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access-9 Large Bore Hemostasis Valves Recalled by Merit Medical Systems,...
The Issue: A design change made to a hemostasis valve to improve manufacturability...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Plus Ventilator (All Models Recalled by Respironics...
The Issue: Ventilator units have an issue impacting an internal electrical circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDTRONIC INTERSTIM THERAPY SYSTEM FOR URINARY CONTROL Recalled by Medtronic...
The Issue: There is a software anomaly with the InterStim X Clinician software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Ventilator (All Models Recalled by Respironics...
The Issue: Ventilator units have an issue impacting an internal electrical circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V680 Ventilator (All Models Recalled by Respironics...
The Issue: Ventilator units have an issue impacting an internal electrical circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NanoSight LM10 fitted with LM14 module. A laboratory instrument for Recalled...
The Issue: Product found to not comply to Class 1 Laser safety requirement.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NanoSight LM10 fitted with LM12 module. A laboratory instrument for Recalled...
The Issue: Product found to not comply to Class 1 Laser safety requirement.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Universal Flexible Arm part number Recalled by Integra LifeSciences...
The Issue: Excess force used to tighten the Universal Flexible Arm can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coryell Memorial Hosp Total Recalled by Stradis Medical, LLC dba Stradis...
The Issue: The outer bag may be perforated or torn, which may result in a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...
The Issue: Product is mislabeled as self-righting Luer slip tip caps, yellow.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ExacTrac Dynamic software model numbers: 20910-01 Recalled by Brainlab AG...
The Issue: The yaw angle may be incorrect for CBCT positioning workflows using setup...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mycoplasma genitalium Control Panel (Inactivated Pellet) Recalled by...
The Issue: Distributed product did not undergo proper release testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo Application software VE20 (Material Number 10848815) installed on the...
The Issue: After CT image data from Toshiba is loaded, image mirroring can occur along...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.