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. 2,600 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
2,600 in last 12 months

Showing 2064120660 of 52,339 recalls

Medical DeviceNovember 6, 2019· Allergan PLC

Recalled Item: Natrelle Inspira Sillicone-Filled Breast Implants for the following Styles...

The Issue: The firm has became aware that 2D barcodes on breast implants and sizers may...

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

Class III — Low RiskOngoing
Medical DeviceNovember 6, 2019· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Color Cuff Disposable Tourniquet Cuff Recalled by Stryker Instruments Div....

The Issue: There is a potential for the cuff to leak air leading to a loss of vascular...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2019· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Color Cuff Disposable Tourniquet Cuff Recalled by Stryker Instruments Div....

The Issue: There is a potential for the cuff to leak air leading to a loss of vascular...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2019· Allergan PLC

Recalled Item: NATRELLE Resterilizable Sizers for the styles and sizes: Style 15 Recalled...

The Issue: The firm has became aware that 2D barcodes on breast implants and sizers may...

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

Class III — Low RiskOngoing
Medical DeviceNovember 6, 2019· Qualigen Inc

Recalled Item: The FastPack System Comlete Immunoassay Kit Immunoassay for the Quantitative...

The Issue: The chemiluminescent immunoassay has been noted to have higher than expected...

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

Class II — Potential Health HazardOngoing
DrugNovember 6, 2019· Golden State Medical Supply Inc.

Recalled Item: GSMS: Ranitidine Capsules 300 mg Recalled by Golden State Medical Supply...

The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2019· AuroMedics Pharma LLC

Recalled Item: Ranitidine Syrup (Ranitidine Oral Solution Recalled by AuroMedics Pharma LLC...

The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2019· AuroMedics Pharma LLC

Recalled Item: DG Health Acid Reducer Ranitidine Tablets 150 mg Recalled by AuroMedics...

The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2019· AuroMedics Pharma LLC

Recalled Item: Aurobindo Ranitidine Caspules 150 mg Recalled by AuroMedics Pharma LLC Due...

The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2019· Golden State Medical Supply Inc.

Recalled Item: GSMS: Ranitidine Capsules 150 mg Recalled by Golden State Medical Supply...

The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2019· AuroMedics Pharma LLC

Recalled Item: Aurobindo Ranitidine Capsules 150 mg Recalled by AuroMedics Pharma LLC Due...

The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2019· AuroMedics Pharma LLC

Recalled Item: Aurobindo Ranitidine Capsules 300 mg Recalled by AuroMedics Pharma LLC Due...

The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 5, 2019· Avanos Medical, Inc.

Recalled Item: Haylard Closed Suction System for Neonates/Pediatrics Recalled by Avanos...

The Issue: Avanos Medical has received reports stating that the central lumen of some 5...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2019· King Systems Corp. dba Ambu, Inc.

Recalled Item: King Vision Video Adapter Size 1/2. Laryngoscope used to examine Recalled by...

The Issue: Exhibiting a reversed image. Although the image may appear normal, the users...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 5, 2019· Dako Denmark A/S

Recalled Item: Dako Autostainer instruments: Autostainer Link 48 Recalled by Dako Denmark...

The Issue: The Autostainer instrument may not have a syringe tray installed which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2019· Collagen Matrix Inc

Recalled Item: GIBSON Healthcare Membrane 6-9 Recalled by Collagen Matrix Inc Due to The...

The Issue: The products may have been packaged with an incorrect Instructions for Use.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2019· Collagen Matrix Inc

Recalled Item: GIBSON Healthcare Membrane Extended Recalled by Collagen Matrix Inc Due to...

The Issue: The products may have been packaged with an incorrect Instructions for Use.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2019· Collagen Matrix Inc

Recalled Item: GIBSON Healthcare Membrane Extended Recalled by Collagen Matrix Inc Due to...

The Issue: The products may have been packaged with an incorrect Instructions for Use.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2019· Collagen Matrix Inc

Recalled Item: GIBSON Healthcare Membrane 6-9 Recalled by Collagen Matrix Inc Due to The...

The Issue: The products may have been packaged with an incorrect Instructions for Use.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2019· Collagen Matrix Inc

Recalled Item: GIBSON Healthcare Membrane 6-9 Recalled by Collagen Matrix Inc Due to The...

The Issue: The products may have been packaged with an incorrect Instructions for Use.

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

Class II — Potential Health HazardOngoing