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. 1,048 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
1,048 in last 12 months

Showing 24621–24640 of 52,339 recalls

FoodOctober 16, 2018· Buddy's Kitchen Inc

Recalled Item: Stir Fry Wrap with Rice Recalled by Buddy's Kitchen Inc Due to Potential...

The Issue: Buddy's Kitchen is recalling several products in response to the McCain...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 16, 2018· Bakkavor Foods USA, Inc.

Recalled Item: Trader Joe's Tomato & Basil Hummus Dip Recalled by Bakkavor Foods USA, Inc....

The Issue: Hummus was recalled due to potential Salmonella and/or Listeria...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 16, 2018· Carl Zeiss Meditec, Inc.

Recalled Item: The PLEX Elite 9000 Recalled by Carl Zeiss Meditec, Inc. Due to Under...

The Issue: Under certain fault conditions, the existing design may expose the operator...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: Argon Medical Devices TRI-JECT Recalled by Argon Medical Devices, Inc Due to...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: Argon Medical Devices Septishield II Recalled by Argon Medical Devices, Inc...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: Argon Medical Devices Double Male LL Adapter Recalled by Argon Medical...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: Argon Medical Devices Hemostasis Valve Recalled by Argon Medical Devices,...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· MED-EL Elektromedizinische Gereate, Gmbh

Recalled Item: MED EL Cochlear Implant System Recalled by MED-EL Elektromedizinische...

The Issue: Devices were distributed despite the Helium-fine leak test results not being...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· MED-EL Elektromedizinische Gereate, Gmbh

Recalled Item: MED EL Cochlear Implant System Recalled by MED-EL Elektromedizinische...

The Issue: Devices were distributed despite the Helium-fine leak test results not being...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: Argon Medical Devices Plugs Recalled by Argon Medical Devices, Inc Due to...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: Argon Medical Devices AHD Luer Lock Cap Recalled by Argon Medical Devices,...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· MED-EL Elektromedizinische Gereate, Gmbh

Recalled Item: MED EL Cochlear Implant System Recalled by MED-EL Elektromedizinische...

The Issue: Devices were distributed despite the Helium-fine leak test results not being...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: (1) Argon Medical Devices Stopcocks Recalled by Argon Medical Devices, Inc...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: (1) Argon Medical Devices Vascuclamp Recalled by Argon Medical Devices, Inc...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Canon Medical System, USA, INC.

Recalled Item: Radrex-i X-Ray System (DRAD-3000E) TFP-4336W (Wireless FPD) Software...

The Issue: software malfunction; It was found when a user performs radiography using...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: (1) Argon Medical Devices Double Female LL Adapter Recalled by Argon Medical...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2018· Smiths Medical ASD Inc.

Recalled Item: Medfusion¿ Model 4000 Syringe Infusion Pump Recalled by Smiths Medical ASD...

The Issue: Customers who utilize PharmGuard¿ Server Software (PGS) with Medfusion¿ 4000...

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

Class II — Potential Health HazardOngoing
DrugOctober 15, 2018· Zero Xtreme USA

Recalled Item: Zero Xtreme Dietary Supplement 30-count capsules. By:Zero Xtreme Registro...

The Issue: Marketed Without an Approved NDA/ANDA: Undeclared Sibutramine

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 15, 2018· Heritage Pharmaceuticals, Inc.

Recalled Item: Cidofovir injection 375 mg/mL (75 mg/mL) vial Injection Recalled by Heritage...

The Issue: Lack of Assurance of Sterility: complaints received about dried powder on...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 15, 2018· Baxter Healthcare Corporation

Recalled Item: Metoprolol Tartrate Injection Recalled by Baxter Healthcare Corporation Due...

The Issue: Failed pH Specifications: Upward shift in the pH of the solution within the...

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

Class III — Low RiskOngoing
Refund