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. 2,624 recalls have been distributed to Arizona in the last 12 months.
Showing 18761–18780 of 52,339 recalls
Recalled Item: TTDEYE (brand) Devil Red Recalled by Chengdu Ai Qin E-commerce Co., Ltd Due...
The Issue: Colored contact lenses were distributed without FDA clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESCAPE ONE Recalled by GE Healthcare, LLC Due to CARESCAPE ONE may not...
The Issue: CARESCAPE ONE may not provide visual and audible alarms for Ventricular...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARTO 3 System (Software Version V7.1.80) Recalled by Biosense Webster...
The Issue: Software defect may result in disapperance of tag sites during recalculation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software versions syngo.CT VB20 or VB20_SP1 in the following systems:...
The Issue: Sporadic problems with the current software may result in scanning workflow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Saniderm ADVANCED HAND SANITIZER Recalled by UVT INC Due to Undeclared Methanol
The Issue: Chemical Contamination: Product contains undeclared methanol.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Computed Tomography X-ray System Recalled by Shanghai United Imaging...
The Issue: The metal edge overlap of the mylar strip in the gantry was uneven, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-ray System Recalled by Shanghai United Imaging...
The Issue: The metal edge overlap of the mylar strip in the gantry was uneven, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-ray System Recalled by Shanghai United Imaging...
The Issue: The metal edge overlap of the mylar strip in the gantry was uneven, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMPOWR Partial Knee Peg Drill Recalled by Encore Medical, LP Due to There...
The Issue: There have been issues experienced with the peg preparation steps,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ClosureFast Micro Introducer Sheath Set Recalled by Argon Medical Devices,...
The Issue: Sterile introducer sheath set manufactured under one lot with different...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMPOWR Partial Knee Peg Drill Guide Recalled by Encore Medical, LP Due to...
The Issue: There have been issues experienced with the peg preparation steps,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity ci series System Control Module (SCM) Recalled by Abbott Gmbh & Co....
The Issue: Quality Control results were not properly evaluated for QC failures.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7-Select Yogurt Pretzels Naturally Flavored Vanilla Crunchy Pretzel Covered...
The Issue: Potential to contain undeclared peanuts
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Gordon Choice Imitation Crab Supreme Style Recalled by Trident Seafoods...
The Issue: Product may contain undeclared egg white.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chembio DPP¿ Micro Reader for use with the DPP¿ COVID-19 Recalled by Chembio...
The Issue: FDA revocation of the Emergency Use Authorization due to performance issues
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chembio DPP COVID-19 IgM/IgG System- Rrapid immunochromatographic test for...
The Issue: FDA revocation of the Emergency Use Authorization due to performance issues
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anjon Bremer Molded Crown. bone fixation fastener for spinal use. Recalled...
The Issue: High rate of galling of one threaded component.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Holder HKHZ 19 for use with Quadrox-i and Quadrox-iD Neonatal Recalled by...
The Issue: Removal for a specific lot, lot number 70128207, of Holder HKHZ 19 for use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chembio DPP¿ Micro Reader II for use with the DPP¿ Recalled by Chembio...
The Issue: FDA revocation of the Emergency Use Authorization due to performance issues
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tasty Drops Recalled by MICHIGAN HERBAL REMEDIES Due to Undeclared Lead
The Issue: Chemical contamination: product contains elevated levels of undeclared lead.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.