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 76817700 of 29,154 recalls

Medical DeviceAugust 26, 2022· Leica Microsystems, Inc.

Recalled Item: Leica Surgical Operating Microscopes Recalled by Leica Microsystems, Inc....

The Issue: During internal testing, Leica Microsystems has become aware of a component...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2022· Leica Microsystems, Inc.

Recalled Item: Leica Surgical Operating Microscopes Recalled by Leica Microsystems, Inc....

The Issue: During internal testing, Leica Microsystems has become aware of a component...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2022· Leica Microsystems, Inc.

Recalled Item: Leica Surgical Operating Microscopes Recalled by Leica Microsystems, Inc....

The Issue: During internal testing, Leica Microsystems has become aware of a component...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2022· Leica Microsystems, Inc.

Recalled Item: Leica Surgical Operating Microscopes Recalled by Leica Microsystems, Inc....

The Issue: During internal testing, Leica Microsystems has become aware of a component...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2022· Philips Respironics, Inc.

Recalled Item: Philips BiPAP A30 Recalled by Philips Respironics, Inc. Due to Motor...

The Issue: Motor assemblies manufactured with nonconforming plastic that contributes to...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 26, 2022· Philips Respironics, Inc.

Recalled Item: Philips BiPAP V30 Auto Recalled by Philips Respironics, Inc. Due to Motor...

The Issue: Motor assemblies manufactured with nonconforming plastic that contributes to...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 26, 2022· Philips Respironics, Inc.

Recalled Item: Philips OmniLab Advanced+ Intl (Flow Gen) Recalled by Philips Respironics,...

The Issue: Motor assemblies manufactured with nonconforming plastic that contributes to...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 26, 2022· Philips Respironics, Inc.

Recalled Item: Philips OmniLab Advanced + with Heated Tube Humidifier Recalled by Philips...

The Issue: Motor assemblies manufactured with nonconforming plastic that contributes to...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 26, 2022· Philips Respironics, Inc.

Recalled Item: Philips BiPAP A40 Recalled by Philips Respironics, Inc. Due to Motor...

The Issue: Motor assemblies manufactured with nonconforming plastic that contributes to...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 26, 2022· Philips Respironics, Inc.

Recalled Item: Philips OmniLab Advanced+ Recalled by Philips Respironics, Inc. Due to Motor...

The Issue: Motor assemblies manufactured with nonconforming plastic that contributes to...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 25, 2022· Zimmer, Inc.

Recalled Item: G7 Acetabular System Recalled by Zimmer, Inc. Due to The outer sterile...

The Issue: The outer sterile package cavity has a corner wall thickness that is below...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista High Density Lipoprotein Cholesterol (HDLC) Flex reagent...

The Issue: Dimension Vista¿ High Density Lipoprotein Cholesterol (HDLC) Potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2022· SenTec AG

Recalled Item: sentec 24 / MARe-SF Multi-Site Attachment Ring Easy Recalled by SenTec AG...

The Issue: Weak skin adhesion.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2022· Abbott Molecular, Inc.

Recalled Item: Abbott Alinity m SARS-CoV-2 CTRL Kit Recalled by Abbott Molecular, Inc. Due...

The Issue: Reports received of an increase of message code 9186 (internal control...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 17, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Magnesium (MG) Flex reagent cartridge Siemens Material Number...

The Issue: Dimension Magnesium (MG) Flex reagent cartridge lots may exhibit imprecision...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 17, 2022· Associates of Cape Cod, Inc.

Recalled Item: Fungitell STAT- IVD Assay for (1 ¿ 3)-~-D-Glucan in Serum Recalled by...

The Issue: Incorrect information on the Fungitell STAT clamshells containing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· ConvaTec, Inc

Recalled Item: ConvaTec Active Life Recalled by ConvaTec, Inc Due to impaired functionality...

The Issue: impaired functionality of the release liner

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· ConvaTec, Inc

Recalled Item: ConvaTec Esteem+ Durahesive Plus Recalled by ConvaTec, Inc Due to impaired...

The Issue: impaired functionality of the release liner

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· ConvaTec, Inc

Recalled Item: ConvaTec Esteem+ Durahesive Plus Recalled by ConvaTec, Inc Due to impaired...

The Issue: impaired functionality of the release liner

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· ConvaTec, Inc

Recalled Item: ConvaTec Active Life Recalled by ConvaTec, Inc Due to impaired functionality...

The Issue: impaired functionality of the release liner

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

Class II — Potential Health HazardOngoing