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. 2,406 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
2,406 in last 12 months

Showing 4904149060 of 52,339 recalls

Medical DeviceMarch 4, 2013· Medtronic Xomed, Inc.

Recalled Item: x1 NIM TriVantage EMG Endotracheal Tube 5.0 mm Recalled by Medtronic Xomed,...

The Issue: In March 2013, Medtronic issued a recall of the NIM TriVantage EMG...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 4, 2013· Philips And Neusoft Medical Systems Co., Ltd.

Recalled Item: NeuViz 16 Multi-Slice CT Scanner System Recalled by Philips And Neusoft...

The Issue: User error of the NeuViz 16 or NeuViz Dual may cause personnel injuries....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2013· Philips And Neusoft Medical Systems Co., Ltd.

Recalled Item: NeuViz Dual series CT Scanner System Recalled by Philips And Neusoft Medical...

The Issue: User error of the NeuViz 16 or NeuViz Dual may cause personnel injuries....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2013· Arrow International Inc

Recalled Item: Arrow/Teleflex Medical Berman Angiographic Balloon Catheter and Reverse...

The Issue: The product specifications sheet, part of the Instructions for Use (IFU),...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2013· CareFusion 213, LLC

Recalled Item: Sepp Recalled by CareFusion 213, LLC Due to An internal review of...

The Issue: An internal review of CareFusion's labeling for preoperative skin prep...

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

Class III — Low RiskOngoing
DrugMarch 2, 2013· Physicians Total Care, Inc.

Recalled Item: Voltaren 1% Gel Recalled by Physicians Total Care, Inc. Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Lot and/or Expiration Date; This recall is...

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

Class III — Low RiskOngoing
Refund
FoodMarch 1, 2013· Jans Enterprises Corp. dba WIRA Corp.

Recalled Item: Jasmine Brand Garlic Flavored Crackers (Krupuk Bawang) Recalled by Jans...

The Issue: Wira Corp. is recalling Jasmine Garlic Flavored Crackers because of...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 1, 2013· Bumble Bee International

Recalled Item: Bumble Bee Brand 5oz Chunk Light Tuna in Vegetable Oil Recalled by Bumble...

The Issue: Bumble Bee Foods, LLC, has issued a voluntary recall on specific codes of...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 1, 2013· Bumble Bee International

Recalled Item: Brunswick and Bumble Bee Brand 5oz Chunk Light Tuna in Water. Recalled by...

The Issue: Bumble Bee Foods, LLC, has issued a voluntary recall on specific codes of...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 1, 2013· Bumble Bee International

Recalled Item: Bumble Bee Brand 5oz Chunk White Albacore in Water Recalled by Bumble Bee...

The Issue: Bumble Bee Foods, LLC, has issued a voluntary recall on specific codes of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 1, 2013· American Medical Systems, Inc.

Recalled Item: AMS 800¿ Urinary Control System. The AMS 800¿ Urinary Control Recalled by...

The Issue: American Medical Systems, Inc. is initiating a recall on two components of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2013· American Medical Systems, Inc.

Recalled Item: AMS 800¿ Urinary Control System. The AMS 800¿ Urinary Control Recalled by...

The Issue: American Medical Systems, Inc. is initiating a recall on two components of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2013· B. Braun Medical, Inc.

Recalled Item: Diacap(R) Ultra Dialysis Fluid Filter Recalled by B. Braun Medical, Inc. Due...

The Issue: There is the potential of the residual moisture of the Diacap Ultra membrane...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: Roche Molecular Systems cobas x 480 System 50 mL reagent reservoir Recalled...

The Issue: Certain lots of Reagent reservoirs, may not have a separation in the lower...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2013· Boston Scientific CRM Corp

Recalled Item: Boston Scientific/Cameron Health SQ-RX Model 1010 subcutaneous pulse...

The Issue: An internal protective fuse can be unintentionally activated while the...

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

Class II — Potential Health HazardOngoing
FoodFebruary 28, 2013· See's Candies Inc.

Recalled Item: See's Candies Recalled by See's Candies Inc. Due to One code of 1.7 oz...

The Issue: One code of 1.7 oz Divinity Easter Eggs with Walnuts may actually contain...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 28, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Mammomat Inspiration - full-field digital mammography Product Usage:...

The Issue: Firm became aware of an unintended behavior when using the Mammomat...

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

Class II — Potential Health HazardOngoing
DrugFebruary 27, 2013· Mutual Pharmaceutical Company, Inc.

Recalled Item: Fenofibric Acid Recalled by Mutual Pharmaceutical Company, Inc. Due to...

The Issue: Labeling: Incorrect instructions; an error in section 5.11 of the patient...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 27, 2013· Mutual Pharmaceutical Company, Inc.

Recalled Item: FIBRICOR (fenofibric acid) Tablets Recalled by Mutual Pharmaceutical...

The Issue: Labeling: Incorrect instructions; an error in section 5.11 of the patient...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 27, 2013· Mutual Pharmaceutical Company, Inc.

Recalled Item: Fenofibric Acid Recalled by Mutual Pharmaceutical Company, Inc. Due to...

The Issue: Labeling: Incorrect instructions; an error in section 5.11 of the patient...

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

Class III — Low RiskOngoing
Refund