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. 2,407 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
2,407 in last 12 months

Showing 4330143320 of 52,339 recalls

Medical DeviceJuly 22, 2014· Abbott Laboratories

Recalled Item: ICT Serum Calibrator . For use in the calibration Recalled by Abbott...

The Issue: ICT Serum Calibrator may generate lower than expected Potassium Quality...

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

Class II — Potential Health HazardOngoing
FoodJuly 22, 2014· River Canyon Retreat

Recalled Item: Organic Carob Powder Recalled by River Canyon Retreat Due to Potential...

The Issue: Firm was notified by supplier of recall or Organic Carob Powder that they...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 22, 2014· Dancing Star LLC

Recalled Item: Carob Supergreens Chunks of Energy (10# ) Recalled by Dancing Star LLC Due...

The Issue: Product may be contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 22, 2014· Dancing Star LLC

Recalled Item: Date Flax with Turmeric Chunks of Energy (10# ) Recalled by Dancing Star LLC...

The Issue: Product may be contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 22, 2014· Dancing Star LLC

Recalled Item: Bulk organic Carob powder (10# ) Recalled by Dancing Star LLC Due to...

The Issue: Product may be contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 21, 2014· Medtronic MiniMed Inc.

Recalled Item: Medtronic MiniMed Guardian Monitor Recalled by Medtronic MiniMed Inc. Due to...

The Issue: Medtronic MiniMed is recalling the Guardian REAL-Time monitors because of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2014· GF Health Products, Inc./d.b.a.Basic American Metal Products

Recalled Item: Zenith Slide W-I-D-E Long Term Care Bed Recalled by GF Health Products,...

The Issue: The bed head deck may fail to elevate as expected during normal operation....

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

Class II — Potential Health HazardOngoing
FoodJuly 21, 2014· American Spoon Foods, Inc.

Recalled Item: American Spoon Food Sour Cherry Marmalade Recalled by American Spoon Foods,...

The Issue: Product may have mold in jar.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 18, 2014· Unique Pharmaceutical, Ltd

Recalled Item: All sterile products within expiry Recalled by Unique Pharmaceutical, Ltd...

The Issue: Lack of Sterility Assurance: A recent FDA inspection revealed poor aseptic...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 18, 2014· Unique Pharmaceutical, Ltd

Recalled Item: N-Acetyl Cysteine 20% 4 mL Vial Stock Code: 4133 Recalled by Unique...

The Issue: Non-Sterility: One lot of N-Acetyl Cysteine vials tested positive for...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 18, 2014· Smith & Nephew, Inc.

Recalled Item: RENASYS EZ/ RENASYS EZ Plus 800 mL canister (w/o CLP) Recalled by Smith &...

The Issue: RENASYS EZ Canisters exhibiting visible evidence of deformation of the inlet...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2014· Smith & Nephew, Inc.

Recalled Item: RENASYS EZ/ RENASYS EZ Plus 250 mL canister with Solidifier Recalled by...

The Issue: RENASYS EZ Canisters exhibiting visible evidence of deformation of the inlet...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2014· Diagnostica Stago, Inc.

Recalled Item: Stago IVD Recalled by Diagnostica Stago, Inc. Due to Diagnostica Stago Inc....

The Issue: Diagnostica Stago Inc. received some customer complaints regarding a...

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

Class III — Low RiskOngoing
Medical DeviceJuly 18, 2014· Smith & Nephew, Inc.

Recalled Item: RENASYS EZ/ RENASYS EZ Plus 800 mL canister with Solidifier Recalled by...

The Issue: RENASYS EZ Canisters exhibiting visible evidence of deformation of the inlet...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2014· Cook Inc.

Recalled Item: CloverSnare 4-Loop Vascular Retrieval Snare. Product is packaged in a...

The Issue: This remedial action is the result of six product complaints associated with...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 17, 2014· Zimmer, Inc.

Recalled Item: Tapered-Screw Vent Implant Recalled by Zimmer, Inc. Due to Zimmer Dental is...

The Issue: Zimmer Dental is recalling the Tapered Screw-Vent Implant because the inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2014· Genesis BPS, LLC.

Recalled Item: Pedi-Pak Pedi-Syringe Filter 30 mL Becton Dickinson Syringe Rx Only Genesis...

The Issue: Genesis BPS is recalling numerous devices since they did not notify the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2014· Genesis BPS, LLC.

Recalled Item: Pedi-Pak Pedi-Syringe Filter 35 mL Monoject Syringe Rx Only Genesis BPS...

The Issue: Genesis BPS is recalling numerous devices since they did not notify the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2014· Genesis BPS, LLC.

Recalled Item: Pedi-Pak Pedi-Syringe Filter 60 mL Becton Dickinson/Monoject Syringe Rx Only...

The Issue: Genesis BPS is recalling numerous devices since they did not notify the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2014· TomoTherapy Incorporated

Recalled Item: TomoTherapy Treatment System Recalled by TomoTherapy Incorporated Due to...

The Issue: Accuray is voluntarily recalling TomoTherapy H Series software versions...

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

Class II — Potential Health HazardOngoing