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. 1,887 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
1,887 in last 12 months

Showing 3006130080 of 52,339 recalls

Medical DeviceMay 30, 2017· ICU Medical, Inc.

Recalled Item: 28 cm (11") PUR Bifuse Ext Set w/6-Port NanoClave¿ Manifold Recalled by ICU...

The Issue: The connection between the Female Luer and the NanoClave¿ manifold has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2017· ICU Medical, Inc.

Recalled Item: 168 cm (66") Appx 2.6 ml Recalled by ICU Medical, Inc. Due to The connection...

The Issue: The connection between the Female Luer and the NanoClave¿ manifold has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2017· ICU Medical, Inc.

Recalled Item: 28 cm (11") PUR Smallbore Ext Set w/6-Port NanoClave¿ Manifold Recalled by...

The Issue: The connection between the Female Luer and the NanoClave¿ manifold has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2017· ICU Medical, Inc.

Recalled Item: Kit w/3 Ext Sets Recalled by ICU Medical, Inc. Due to The connection between...

The Issue: The connection between the Female Luer and the NanoClave¿ manifold has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2017· ICU Medical, Inc.

Recalled Item: PROXIMALE - 28 cm (11") Smallbore Ext Set w/6-Port NanoClave¿ Manifold...

The Issue: The connection between the Female Luer and the NanoClave¿ manifold has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2017· ICU Medical, Inc.

Recalled Item: 18 cm (7") PUR Smallbore Ext Set w/6-Port NanoClave¿ Manifold Recalled by...

The Issue: The connection between the Female Luer and the NanoClave¿ manifold has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2017· ICU Medical, Inc.

Recalled Item: 10" Smallbore Ext Set w/6-Port NanoClave¿ Manifold (Orange Recalled by ICU...

The Issue: The connection between the Female Luer and the NanoClave¿ manifold has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2017· ICU Medical, Inc.

Recalled Item: 10" Smallbore Ext Set w/6-Port NanoClave¿ Manifold Recalled by ICU Medical,...

The Issue: The connection between the Female Luer and the NanoClave¿ manifold has the...

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

Class II — Potential Health HazardOngoing
DrugMay 26, 2017· American Pharmaceutical Ingredients LLC

Recalled Item: Methocarbamol Recalled by American Pharmaceutical Ingredients LLC Due to...

The Issue: CGMP Deviations: Lack of quality assurance at the API manufacturer.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 26, 2017· Monfitello

Recalled Item: PRIVATE SELECTION AFRICAN - INSPIRED PERI PERI CHILI CULINARY SPICE Recalled...

The Issue: The firm was notified that the product may contain peanuts.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 26, 2017· Monfitello

Recalled Item: Private Selection Peruvian Inspired Aji Amarillo Culinary Spice Paste NET...

The Issue: The firm was notified that the product may contain peanuts.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 25, 2017· California Sun Dry Foods

Recalled Item: California Sun Dry Sun Dried Tomato Pesto Recalled by California Sun Dry...

The Issue: Firm employee noticed that incorrect back label was attached to Sun-Dried...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 25, 2017· Exactech, Inc.

Recalled Item: EXACTECH Equinoxe Narrow Modular Reverse Pilot-Tip Reamer // Catalog #:...

The Issue: Instructions for use (IFU) is updated to clarify the proper technique and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2017· Exactech, Inc.

Recalled Item: EXACTECH Equinoxe Reverse Starter Reamer - Catalog #: 321-05-01 Recalled by...

The Issue: Instructions for use (IFU) is updated to clarify the proper technique and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2017· Exactech, Inc.

Recalled Item: EXACTECH Equinoxe Narrow Modular Reverse Pilot-Tip Starter Reamer Catalog #:...

The Issue: Instructions for use (IFU) is updated to clarify the proper technique and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2017· Exactech, Inc.

Recalled Item: EXACTECH Equinoxe Modular Reverse Pilot-Tip Reamer Recalled by Exactech,...

The Issue: Instructions for use (IFU) is updated to clarify the proper technique and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2017· Exactech, Inc.

Recalled Item: EXACTECH Equinoxe Glenoid Reamer - Catalog #: 321-05-38 Recalled by...

The Issue: Instructions for use (IFU) is updated to clarify the proper technique and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2017· Exactech, Inc.

Recalled Item: EXACTECH Equinoxe Modular Reverse Pilot-Tip Starter Reamer - Catalog #:...

The Issue: Instructions for use (IFU) is updated to clarify the proper technique and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2017· Exactech, Inc.

Recalled Item: Logic Fit Tibial Tamp Head Recalled by Exactech, Inc. Due to The firm...

The Issue: The firm determined that the labeling (surgical technique) should be updated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2017· Carestream Health Inc

Recalled Item: DRX-Revolution Mobile X-Ray System Recalled by Carestream Health Inc Due to...

The Issue: Carestream found a single unit where four screws in the assembly were not...

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

Class II — Potential Health HazardOngoing