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. 1,762 recalls have been distributed to Arizona in the last 12 months.
Showing 47601–47620 of 52,339 recalls
Recalled Item: EZTest Steam Biological Indicator Recalled by Steritec Products Mfc. Co.,...
The Issue: Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona (TM) The Personalized Knee System CR Tibial Articular Surface...
The Issue: Zimmer had received complaints that reported breakage of the Persona Knee...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Afinity CQ2015A Intraocular Lens The visual correction of aphakia in...
The Issue: STAAR Surgical Company is recalling a limited number of nanoFLEX CC4204A and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Osseotite 2 Certain Prevail 5mm(D)X 4.1mm (P) X X 11.5mm Recalled by Biomet...
The Issue: One of the dental implants do not have the internal hex feature. One of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Instrument Control Box Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Factory testing on da Vinci Si Surgical Systems may not be in compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Si Vision System Cart Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Factory testing on da Vinci Si Surgical Systems may not be in compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Si Surgeon Side Cart Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Factory testing on da Vinci Si Surgical Systems may not be in compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Dual Camera Controller Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Factory testing on da Vinci Si Surgical Systems may not be in compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 90597002009 Articular Surface CR ART SURF 12/PURPLE 09MM Recalled by Zimmer,...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed Paradigm Insulin Infusion Sets The Paradigm infusion sets...
The Issue: Medtronic is recalling the Medtronic MiniMed Paradigm Medtronic is recalling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Programmable Infusion Pump Recalled by Codman & Shurtleff, Inc....
The Issue: Miscalibrated Fill Level Sensor may affect dosing level
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Programmable Infusion Pump- Implantable for the intrathecal...
The Issue: Miscalibrated Fill Level Sensor may affect dosing level
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Basal/Bolus Infusor. Indicated for the intravenous...
The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 90597003109 Articular Surface CR ART SURF 34/STR YEL 09MM Recalled by...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 65595201201 Femur CR-FLEX POR HATCP FEM B-L Rx Recalled by Zimmer, Inc. Due...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597002009 Articular Surface CR ART SURF 12/PURPLE 9 Recalled by Zimmer,...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00595601201 Femur CR-FLEX OPT FEM B-L Rx Sterile Recalled by Zimmer, Inc....
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 90597004109 Articular Surface CR ART SURF AE56/STR GRN 09MM Recalled by...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597001303 Femur CR PRC FEM COMP SIZE CML Rx Recalled by Zimmer, Inc. Due...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597206126 Patella ALL POLY PAT COMP MICRO 26DIA Recalled by Zimmer, Inc....
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.