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. 1,938 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
1,938 in last 12 months

Showing 1672116740 of 29,154 recalls

Medical DeviceMarch 12, 2018· Hamilton Medical AG

Recalled Item: Hamilton-C2 Ventilator Unit Intended to provide ventilator support to adults...

The Issue: After two and a half years, the battery fuel gauge may indicate a higher...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· Ohio Medical Corporation

Recalled Item: Vacuum Regulator Recalled by Ohio Medical Corporation Due to Final quality...

The Issue: Final quality control testing was not completed before the devices were...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2018· Stryker GmbH

Recalled Item: Hinge Coupling Hoffmann LRF Catalog # 4933-0-800 Intended for fixation...

The Issue: The wrong parts were picked for packaging. The connecting Nuts were packed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Edwards Lifesciences Optisite Arterial Perfusion Cannula Recalled by SPS...

The Issue: The expiration date on the device labeling exceeds its actual validated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Boston Scientific Wallstent RP Endoprosthesis Tracheobronchial...

The Issue: The expiration date on the device labeling exceeds its actual validated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Boston Scientific Wallstent Endoprosthesis Tracheobronchial Self-Expanding...

The Issue: The expiration date on the device labeling exceeds its actual validated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Vascular Solutions Venture Rx Catheter Recalled by SPS Sterilization, Inc...

The Issue: The expiration date on the device labeling exceeds its actual validated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Boston Scientific Wallstent RP Endoprosthesis Tracheobronchial Transhepatic...

The Issue: The expiration date on the device labeling exceeds its actual validated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· Ethicon, Inc.

Recalled Item: Evicel Accessory Device - 45 cm Flexible Tip (SET OF 3) Recalled by Ethicon,...

The Issue: Products labeled for distribution outside the United States may have been...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· Intuitive Surgical, Inc.

Recalled Item: da Vinci X Surgical System Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Specific da Vinci X Surgical Systems (IS4200) were shipped with defective...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Edwards Lifesciences EZ Glide Aortic Cannula Recalled by SPS Sterilization,...

The Issue: The expiration date on the device labeling exceeds its actual validated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Edwards Lifesciences Femoral Venous Cannula Recalled by SPS Sterilization,...

The Issue: The expiration date on the device labeling exceeds its actual validated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Edwards Lifesciences Thin-Flex Single Stage Venous Drainage Cannula Recalled...

The Issue: The expiration date on the device labeling exceeds its actual validated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Edwards Lifesciences Avid Dual Stage Venous Drainage Cannula Recalled by SPS...

The Issue: The expiration date on the device labeling exceeds its actual validated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Edwards Lifesciences Thin-Flex Single Stage Venous Drainage Cannula Recalled...

The Issue: The expiration date on the device labeling exceeds its actual validated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Edwards Lifesciences Aortic Perfusion Cannula Recalled by SPS Sterilization,...

The Issue: The expiration date on the device labeling exceeds its actual validated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Boston Scientific Wallstent Endoprosthesis Tracheobronchial Transhepatic...

The Issue: The expiration date on the device labeling exceeds its actual validated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Boston Scientific Wallstent Enteral Endoprosthesis Colonic/Duodenal Stent...

The Issue: The expiration date on the device labeling exceeds its actual validated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Boston Scientific Wallstent Endoprosthesis Tracheobronchial Self-Expanding...

The Issue: The expiration date on the device labeling exceeds its actual validated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2018· SPS Sterilization, Inc

Recalled Item: Edwards Lifesciences Femoral Venous Cannula Recalled by SPS Sterilization,...

The Issue: The expiration date on the device labeling exceeds its actual validated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing