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 13761–13780 of 29,154 recalls
Recalled Item: Alpha Conducting solution product codes:3310-15 ACS - Product Usage:...
The Issue: Potential for failed stability antimicrobial effectiveness testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual-Sided Interhemispheric Recalled by Ad-Tech Medical Instrument...
The Issue: Supplemental information provided with devices indicates that the subdural...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Depth Electrodes Recalled by Ad-Tech Medical Instrument Corporation Due to...
The Issue: Supplemental information provided with devices indicates that the subdural...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Skull Anchor Bolts Recalled by Ad-Tech Medical Instrument Corporation Due to...
The Issue: Supplemental information provided with devices may indicate that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LSB Style Anchor Bolt. Labeled with the following parts: 13mm Recalled by...
The Issue: On June 12, 2019 Ad-Tech was made aware that on three different occasions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Serrato 9.5mm X 90mm Polyaxial Screw Catalog Number 482619590 Serrato...
The Issue: Discrepant length; Lot B88751 90mm screws were manufactured with a 100mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEEP Precision Integrated System 120V & LEEP Precision Generator Recalled by...
The Issue: The products' cut, coagulate, or blend function may not operate with the use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Surgical System Recalled by Intuitive Surgical, Inc. Due to One da...
The Issue: One da Vinci Xi Endoscope Controller in the field was improperly calibrated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products GLU Slides-Product Code:1707801. IVD VITROS...
The Issue: Potentially Biased Results using VITROS Chemistry Products GLU Slides
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS100 Intra-Aortic Balloon Pump Recalled by Datascope Corp. Due to If...
The Issue: If battery maintenance is not performed appropriately, the battery may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS100 Intra-Aortic Balloon Pump Recalled by Datascope Corp. Due to If...
The Issue: If battery maintenance is not performed appropriately, the battery may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS300 Intra-Aortic Balloon Pump Recalled by Datascope Corp. Due to If...
The Issue: If battery maintenance is not performed per instructions, the battery may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: Battery short-run times and unanticipated stoppage may be due to user not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS300 Intra-Aortic Balloon Pump Recalled by Datascope Corp. Due to If...
The Issue: If battery maintenance is not performed per instructions, the battery may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue IABP Recalled by Datascope Corp. Due to If battery...
The Issue: If battery maintenance is not performed appropriately, the battery may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EQUISTREAM¿ XK Long-Term Hemodialysis Catheter....
The Issue: Incorrect Peel-Apart Introducer Sheath in Kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EQUISTREAM¿ XK Long-Term Hemodialysis Catheter....
The Issue: Incorrect Peel-Apart Introducer Sheath in Kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Babi.Plus 12.5 cm H2O Pressure Relief Manifold Catalog # 2691 Recalled by...
The Issue: Device vented gas below the stated pressure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STANLEY Healthcare Arial 54315 Network Manager Recalled by Stanley Security...
The Issue: STANLEY Healthcare has received reports of outages on the Arial nurse call...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advincula Delineator with Ultem Plastic Soft Cup size 3.0 cm Recalled by...
The Issue: The soft, flexible cup of the Advincula Delineator may be unvalidated and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.