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 4178141800 of 52,339 recalls

Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: (R)IR remote control JUPITER Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: Cable remote control JUPITER Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Leonhard Lang Gmbh

Recalled Item: GE Healthcare Pediatric Direct-Wired Disposable Defibrillation/Pacing...

The Issue: The firm discovered that during the use of these defibrillation electrodes a...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 3, 2014· Iris Diagnostics

Recalled Item: RTH8 Rotor Recalled by Iris Diagnostics Due to Iris International is...

The Issue: Iris International is recalling the RTH8 Rotor used in the StatSpin Express...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Teleflex Medical

Recalled Item: WECK Hemoclip¿ Traditional Medium Tantalum Ligating Clips. Weck Ligating...

The Issue: The manufacturing dates and expiration dates were transposed on the Tyvek label.

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

Class II — Potential Health HazardOngoing
FoodDecember 2, 2014· ReNew Life Formulas, Inc.

Recalled Item: PureLife Naturals Adult Multi-Plus Multi-Vitamins & Minerals Plus Herbs...

The Issue: Labels indicate "no wheat" "no gluten" and the products contain gluten and...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 2, 2014· ReNew Life Formulas, Inc.

Recalled Item: PureLife Naturals Multi-Action Immunity 90 Pure-Caps HDPE bottle Recalled by...

The Issue: Labels indicate "no wheat" "no gluten" and the products contain gluten and...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 2, 2014· Overhill Farms Inc

Recalled Item: Open Nature Chile Cheese Enchilada Two enchiladas filled with a Recalled by...

The Issue: A recall notice from High Quality Organics (HQO) recalling their organic...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 2, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Linear Accelerator: ARTISTE Recalled by Siemens Medical Solutions...

The Issue: Use of any unauthorized third-party components on Siemens LINACs may lead to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2014· Vyaire Medical

Recalled Item: Adult AirLife dual-limb Recalled by Vyaire Medical Due to Manufacturing...

The Issue: Manufacturing error in humidification chamber may cause an overfill/overflow...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 29, 2014· Vyaire Medical

Recalled Item: Infant AirLife single-limb Recalled by Vyaire Medical Due to Manufacturing...

The Issue: Manufacturing error in humidification chamber may cause an overfill/overflow...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 29, 2014· Vyaire Medical

Recalled Item: Infant AirLife Dual- Recalled by Vyaire Medical Due to Manufacturing error...

The Issue: Manufacturing error in humidification chamber may cause an overfill/overflow...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 29, 2014· Vyaire Medical

Recalled Item: Adult Air-Life single-limb circuit (Model AH202) with AirLife Humidification...

The Issue: Manufacturing error in humidification chamber may cause an overfill/overflow...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 29, 2014· Magellan Diagnostics, Inc.

Recalled Item: Magellan Diagnostics LeadCare Ultra Blood Analyzer Part Number: 80-0010...

The Issue: LeadCare Plus and LeadCare Ultra Blood Lead Testing Systems may generate...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 29, 2014· Magellan Diagnostics, Inc.

Recalled Item: Magellan Diagnostics LeadCare Ultra Blood Lead Test Kits Part Number:...

The Issue: LeadCare Plus and LeadCare Ultra Blood Lead Testing Systems may generate...

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

Class I — Serious Health HazardOngoing
FoodNovember 28, 2014· The Santa Barbara Smokehouse, Inc.

Recalled Item: Cambridge House Balmoral Thinly Sliced Exceptional Ready to Enjoy Smoked...

The Issue: The firm was notified by two customers of two lot/batch numbers testing...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 26, 2014· Zydus Pharmaceuticals USA Inc

Recalled Item: Benzonatate Capsules Recalled by Zydus Pharmaceuticals USA Inc Due to Failed...

The Issue: Failed Tablet/Capsule Specifications: Recall due to wet and/or leaking capsules.

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 26, 2014· fgf brands, inc

Recalled Item: Mini Naan Eight (8) nann packaged in coated paper printed Recalled by fgf...

The Issue: The products were shipped without labels declaring the nutrition and...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 26, 2014· SCC Soft Computer

Recalled Item: SoftPath Laboratory Information System. Versions 4.3.0.8 Recalled by SCC...

The Issue: Modifications to diagnostic text may be: 1) Saved to the database but not...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2014· Lacrimedics Inc

Recalled Item: VisiPlugST for the Lacrimal Efficiency Test. It is also sold Recalled by...

The Issue: Moisture level may cause the VisiPlugST (or CollaSyn Plugs) to break apart,...

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

Class III — Low RiskOngoing