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. 2,406 recalls have been distributed to Arizona in the last 12 months.
Showing 51141–51160 of 52,339 recalls
Recalled Item: Centricity PACS IW by GE Healthcare Dynamic Imaging Solutions is Recalled by...
The Issue: Multiple issues were identified with the GE Centricity PACS-IW system that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA Satellite Automated Multi-Parameter Analyzer This system is a fully...
The Issue: Following a single customer complaint that incorrect INR values were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Module Model 8100 (formerly Medley Pump Module) Subsequent...
The Issue: The recall was initiated because Carefusion has identified a potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hitachi Echelon MRI System/Oasis MRI Recalled by Hitachi Medical Systems...
The Issue: Hitachi discovered a software error with a feature called Multi-Planar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AngioDynamics Angiographic catheter --- Soft-Vu (JB-1) Non-braided. ---...
The Issue: AngioDynamics is recalling one lot of Soft-Vu Angiographic catheters because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZEE Antiseptic Wipes Recalled by Dukal Corp. Due to Microbial contamination...
The Issue: Microbial contamination of Non Sterile Product; contamination with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dukal Corporation BZK Swab Recalled by Dukal Corp. Due to Microbial...
The Issue: Microbial contamination of Non Sterile Product; contamination with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kleenex Luxury Foam Hand Sanitizer Recalled by Kimberly-Clark Corporation...
The Issue: Microbial Contamination of Non-Sterile Products; The affected lots were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kleenex Foam Hand Sanitizer Recalled by Kimberly-Clark Corporation Due to...
The Issue: Microbial Contamination of Non-Sterile Products; The affected lots were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sonoran Rice Recalled by Namias dba Chonita Foods Due to The product was...
The Issue: The product was recalled due to undeclared-sub ingredient, hydrolyzed soy...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: IQF Oysters 3lbs Recalled by KOREAN FARM, INC. Due to Korean Farm is...
The Issue: Korean Farm is recalling Assi Brand Korean Oysters because they have been...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The 2.7mm Drilling Guide is a reusable instrument used in Recalled by...
The Issue: Integra' s quality system noted an adverse trend in complaints for breakage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Xcelera Connect Recalled by Philips Healthcare Inc. Due to Xcelera...
The Issue: Xcelera Connect R2.1 L 1 SP2 , incomplete information arriving from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ocean Manna Korean IQF Oysters Recalled by Pacific Giant, Inc Due to Pacific...
The Issue: Pacific Giant is recalling all frozen (IQF) oyster meat and 1/2 shell...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE has become aware of...
The Issue: GE has become aware of multiple issues affecting the Dash 3000/4000/5000 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE has become aware of...
The Issue: GE has become aware of multiple issues affecting the Dash 3000/4000/5000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: seprafilm¿ Procedure Pack ADHESION BARRIER Re-order Number: 5086-02 Product...
The Issue: Sterility of product may be compromised due to packaging defect
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: seprafilm¿ Single Site ADHESION BARRIER Re-order Number: 6641-01 Product...
The Issue: Sterility of product may be compromised due to packaging defect
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fuze Manual Tilt Wheelchair. Fuze T50 Recalled by Pdg Product Design Group...
The Issue: The hex bolt head might shear and cause the axle plate to detach from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX iD HMOD 2030 Diffusion Membrane Oxygenator Recalled by Maquet...
The Issue: It has come to firm's attention that, in some rare cases, the blood outlet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.