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. 2,759 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
2,759 in last 12 months

Showing 79417960 of 52,339 recalls

Medical DeviceOctober 9, 2023· Philips North America Llc

Recalled Item: Brilliance CT Big Bore Oncology with software version V4.8.0.10421...

The Issue: For oncology users: If the user performed off-set reconstruction on CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Philips Ultrasound, Inc.

Recalled Item: Philips Affiniti 70 Recalled by Philips Ultrasound, Inc. Due to Their is the...

The Issue: Their is the potential that diagnostic ultrasound systems operating with...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Philips Ultrasound, Inc.

Recalled Item: Philips EPIQ Diagnostic Ultrasound System Models: EPIQ 7G(model # 795200)...

The Issue: Their is the potential that diagnostic ultrasound systems operating with...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2023· Advance-Esthetic LLC

Recalled Item: MED-810A Zemits NDPrime Laser products Recalled by Advance-Esthetic LLC Due...

The Issue: Advance-Esthetic LLC failed to comply with the applicable standards...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2023· Peter Lazic Gmbh

Recalled Item: D-Clip Standard/Mini Applier Recalled by Peter Lazic Gmbh Due to Customer...

The Issue: Customer complaint received that reported the applier failed during surgery....

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2023· Peter Lazic Gmbh

Recalled Item: D-Clip Standard/Mini Applier Recalled by Peter Lazic Gmbh Due to Customer...

The Issue: Customer complaint received that reported the applier failed during surgery....

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2023· Peter Lazic Gmbh

Recalled Item: D-Clip Standard/Mini Applier Recalled by Peter Lazic Gmbh Due to Customer...

The Issue: Customer complaint received that reported the applier failed during surgery....

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2023· LEONI CIA CABLE SYSTEMS

Recalled Item: ORION System with software OSS v6.0 and OSS v7.0- An Recalled by LEONI CIA...

The Issue: Users of the patient positioning system ORION System can be faced with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2023· LEONI CIA CABLE SYSTEMS

Recalled Item: ORION System with software OSS v6.0 and OSS v7.0- An Recalled by LEONI CIA...

The Issue: Users of the patient positioning system ORION System can be faced with a...

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

Class II — Potential Health HazardOngoing
DrugOctober 5, 2023· Dollar Tree Distribution, Inc.

Recalled Item: Certain Over-The-Counter (OTC) drug products sold by Family Dollar retail...

The Issue: CGMP Deviations: OTC products were stored outside of labeled temperature...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 5, 2023· CareFusion 303, Inc.

Recalled Item: MEDFLEX Recalled by CareFusion 303, Inc. Due to If "Clear All" selected...

The Issue: If "Clear All" selected medications is selected on patient profile, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2023· Encore Medical, LP

Recalled Item: Recalled by Encore Medical, LP Due to Mislabeling

The Issue: Mislabeling

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2023· Encore Medical, LP

Recalled Item: Reverse Shoulder System e+ Recalled by Encore Medical, LP Due to Mislabeling

The Issue: Mislabeling

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2023· Integra LifeSciences Corp.

Recalled Item: CereLink ICP Extension Cable (Extension Cable) Recalled by Integra...

The Issue: Firm is expanding the existing recall RES 90457 for the Cerelink, initiated...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 5, 2023· Siemens Medical Solutions USA, Inc

Recalled Item: Mobilett Mira wireless (VA20) mobile x-ray system(s) Recalled by Siemens...

The Issue: Due to the incorrect mounting of the buzzer component, there is no acoustic...

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

Class II — Potential Health HazardOngoing
DrugOctober 4, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Clinical TREAT Antifungal Powder Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: CGMP deviations: the product was shipped from the Manufacturer to a Medline...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 4, 2023· Denver Solutions, LLC DBA Leiters Health

Recalled Item: VANCOmycin HCI PF Recalled by Denver Solutions, LLC DBA Leiters Health Due...

The Issue: Labeling: Not Elsewhere Classified

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugOctober 4, 2023· Denver Solutions, LLC DBA Leiters Health

Recalled Item: VANCOmycin HCI PF Recalled by Denver Solutions, LLC DBA Leiters Health Due...

The Issue: Labeling: Not Elsewhere Classified

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugOctober 4, 2023· Denver Solutions, LLC DBA Leiters Health

Recalled Item: Oxytocin synthetic Recalled by Denver Solutions, LLC DBA Leiters Health Due...

The Issue: Labeling: Not Elsewhere Classified

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugOctober 4, 2023· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Bupropion Hydrochloride Extended-Release Tablets USP (SR) Recalled by SUN...

The Issue: Failed Dissolution Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund