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. 2,725 recalls have been distributed to Arizona in the last 12 months.
Showing 13341–13360 of 29,154 recalls
Recalled Item: Transducer S8-3t UDI (01)00884838073524 Can be used as Recalled by Philips...
The Issue: The firm has discovered an issue associated with some Transesophageal (TEE)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dario Blood Glucose Monitoring System Recalled by LABSTYLE INNOVATIONS Due...
The Issue: The Dario-Blood Glucose Tracker Android App versions 4.3.0-4.3.2 may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion CIRCLAMP W/1.3 CM BELL-single-use Recalled by Centurion Medical...
The Issue: A mismatch between the angle of the hole in the base and the angle of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas c 311 Recalled by Roche Diagnostics Operations, Inc. Due to Tina-quant...
The Issue: Tina-quant Soluble Transferrin Receptor (STFR) Assays Updated Claims for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion CIRCLAMP W/1.1CM BELL - single-use Recalled by Centurion Medical...
The Issue: A mismatch between the angle of the hole in the base and the angle of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas c 701 and 702 Analyzer/Module-RF interference claims for the Recalled...
The Issue: Tina-quant Soluble Transferrin Receptor (STFR) Assays Updated Claims for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AD-TECH Drill Sleeve Guides Recalled by Ad-Tech Medical Instrument...
The Issue: The inner diameter of the drill sleeve guide raw material was found to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz Recalled by Karl Storz Endoscopy Due to During a complaint...
The Issue: During a complaint investigation it was determined that an error was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Low Volume Cartridge IFU (SKU CAR-125-B) used with the following Recalled by...
The Issue: There is a potential patient health risk while performing chronic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz NEURO-FIBERSCOPE Recalled by Karl Storz Endoscopy Due to During a...
The Issue: During a complaint investigation it was determined that an error was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz RHINO-LARYNGO-BRONCHO FIBERSCOPE Recalled by Karl Storz Endoscopy...
The Issue: During a complaint investigation it was determined that an error was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Positron Emission Tomograpy and Computed Tomography System Recalled by...
The Issue: Potential sporadic software bugs in R001.3.0.0.750505 software version may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pharos Excimer Laser Recalled by Ra Medical Systems, Inc. Due to At doses of...
The Issue: At doses of less than 100 mJ, in custom and auto repeat modes, a software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue 1.4 GHz Remote Antenna Used with Philips MX4O Monitors-The...
The Issue: Remote Antenna Cable Used with Philips MX4O Monitors Does Not Have the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CentriMag Acute Circulatory Support System Motor Recalled by Thoratec...
The Issue: Reports have been received of the CentriMag Systems experiencing motor and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VNS Therapy Recalled by LivaNova USA Inc Due to Sentiva generators may reset...
The Issue: Sentiva generators may reset and become disabled within 60 days of enabling....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COMP RVRS Shoulder Baseplates Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.0MM BALL NOSE GUIDE WIRE Recalled by Zimmer Biomet, Inc. Due to Elevated...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CEZANNE II TLIF Bullet-Tip Cage Recalled by CTL Medical Corporation Due to...
The Issue: Reports received of the device fracturing during insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Recalled by Zimmer Biomet, Inc. Due to Elevated levels of bacterial...
The Issue: Elevated levels of bacterial endotoxin and residual debris remain on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.