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. 2,782 recalls have been distributed to Arizona in the last 12 months.
Showing 4321–4340 of 29,154 recalls
Recalled Item: Jackson-Pratt 3-Spring Reservoir with Silicone Adapters Recalled by Cardinal...
The Issue: Cardinal Health is issuing a lot number specific voluntary removal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jackson-Pratt 3-Spring Reservoir Kit with PVC Round Drain Recalled by...
The Issue: Cardinal Health is issuing a lot number specific voluntary removal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jackson-Pratt Universal Connector PVC Tubing Anti Transparent Y Recalled by...
The Issue: Cardinal Health is issuing a lot number specific voluntary removal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jackson-Pratt 3-Spring Reservoir Kit with PVC Round Drain Recalled by...
The Issue: Cardinal Health is issuing a lot number specific voluntary removal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jackson-Pratt 3-Spring Reservoir Kit with PVC Round Drain Recalled by...
The Issue: Cardinal Health is issuing a lot number specific voluntary removal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BiPAP V30 Auto Ventilator Recalled by Philips Respironics, Inc. Due to...
The Issue: Potential for devices to experience interruption/loss of therapy during a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BiPAP A40 Ventilators: BiPAP A40 Recalled by Philips Respironics, Inc. Due...
The Issue: Potential for devices to experience interruption/loss of therapy during a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BiPAP A30 Ventilator Recalled by Philips Respironics, Inc. Due to Potential...
The Issue: Potential for devices to experience interruption/loss of therapy during a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stealth S8 Clinical Software Application Recalled by Medtronic Navigation,...
The Issue: Due to a software issue, there is the potential for a missing digit, letter,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POLYSIN (Polyglycolic Acid) suture Recalled by SURGICAL SPECIALTIES Due to...
The Issue: Complaints have been received with allegations of Incorrect Needle Curvature.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RKN130002 Recalled by Ossur H / F Due to Due to firmware issues with the...
The Issue: Due to firmware issues with the prosthetic knee, there is the potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RKNXC0005 Recalled by Ossur H / F Due to Due to firmware issues with the...
The Issue: Due to firmware issues with the prosthetic knee, there is the potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RKNXC0003 Recalled by Ossur H / F Due to Due to firmware issues with the...
The Issue: Due to firmware issues with the prosthetic knee, there is the potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RKN130003 Recalled by Ossur H / F Due to Due to firmware issues with the...
The Issue: Due to firmware issues with the prosthetic knee, there is the potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AW-M0001 SONARMED MONITOR. Used in conjunction with SonarMed Acoustic...
The Issue: Software anomaly resulted in failure to detect a partial obstruction in 2.5...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5000 Compact Series Ultrasound Systems Recalled by Philips Ultrasound, Inc....
The Issue: Ultrasound system with: 1) transesophageal echocardiography transducer (TEE)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINER Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to A slight...
The Issue: A slight dimensional variation which has the potential for increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINER Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to A slight...
The Issue: A slight dimensional variation which has the potential for increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure kits labeled as follows: a) HEART ANESTHESIA SET...
The Issue: A slight dimensional variation which has the potential for increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1 Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to A slight...
The Issue: A slight dimensional variation which has the potential for increased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.