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. 1,897 recalls have been distributed to Arizona in the last 12 months.
Showing 28101–28120 of 29,154 recalls
Recalled Item: The Eon Mini Implantable Pulse Generator (IPG) is a 16-channel Recalled by...
The Issue: Eon Mini IPGs manufactured in April 2012 could potentially exhibit a sudden,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sirus¿ intramedullary nail for tibia Recalled by Zimmer, Inc. Due to Zimmer...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dynesys¿ Universal spacer 6-45 Recalled by Zimmer, Inc. Due to Zimmer Inc.,...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dynesys¿ Set screw M6 Recalled by Zimmer, Inc. Due to Zimmer Inc., is...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wagner SL Revision Stem Recalled by Zimmer, Inc. Due to Zimmer Inc., is...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MS-30¿ Proximal positioner Recalled by Zimmer, Inc. Due to Zimmer Inc., is...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Metasul¿ Durom¿ Femoral component Sterile Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anatomical Shoulder" Fracture Humeral Head Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NCB¿-PH Plate Recalled by Zimmer, Inc. Due to Zimmer Inc., is initiating a...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dynesys¿ HA Pedicle + set screw Recalled by Zimmer, Inc. Due to Zimmer Inc.,...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anatomical Shoulder" Revision Humeral stem Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLS Stem Recalled by Zimmer, Inc. Due to Zimmer Inc., is initiating a...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anatomical Shoulder" Fracture Humeral stem Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NCB¿ screw ¿ 4.0 self-tapping Recalled by Zimmer, Inc. Due to Zimmer Inc.,...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MS-30 Shaft Recalled by Zimmer, Inc. Due to Zimmer Inc., is initiating a...
The Issue: Zimmer Inc., is initiating a correction to the patient labels of products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multipolar¿ Bipolar Cup Liner 22 mm LD. Recalled by Zimmer, Inc. Due to...
The Issue: Zimmer Inc. is initiating a removal of the Multipolar¿ Bipolar Cup Liner 22...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wound Pro Apex Negative Pressure Wound Therapy Powered Suction Pump Recalled...
The Issue: Accuro has received reports of some Apex Pumps either failing to operate or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Brilliance CT Big Bore is a whole-body Computed Tomography Recalled by...
The Issue: Philips Healthcare received a complaint stating the system opens e-stop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATLANTIS(R) Anterior Cervical Plate System VARIABLE ANGLE SCREW MODULE...
The Issue: Lines on the screw gauge may not placed on the caddy properly which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATLANTIS(R) Anterior Cervical Plate System FIXED ANGLE SCREW MODULE Recalled...
The Issue: Lines on the screw gauge may not placed on the caddy properly which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.