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. 2,571 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
2,571 in last 12 months

Showing 3088130900 of 52,339 recalls

Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· Vyaire Medical

Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...

The Issue: The mask component on various lots of the resuscitation devices have been...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 27, 2017· AbbVie Inc.

Recalled Item: AbbVie PEG Recalled by AbbVie Inc. Due to PEG kits have the potential for...

The Issue: PEG kits have the potential for one of the following defects: missing...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2017· AbbVie Inc.

Recalled Item: AbbVie PEG Recalled by AbbVie Inc. Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2017· AbbVie Inc.

Recalled Item: AbbVie PEG Recalled by AbbVie Inc. Due to PEG kits have the potential for...

The Issue: PEG kits have the potential for one of the following defects: missing...

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

Class II — Potential Health HazardOngoing
FoodApril 27, 2017· Lords Organics Llc

Recalled Item: Organic Veda brand Ginger Powder Recalled by Lords Organics Llc Due to...

The Issue: Lord Organics is recalling ginger powder because it has the potential to be...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 27, 2017· Hetero USA Inc

Recalled Item: Acyclovir Tablets Recalled by Hetero USA Inc Due to Presence of Foreign...

The Issue: Presence of Foreign Substance: human hair melded into tablet.

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

Class III — Low RiskOngoing
Refund
DrugApril 27, 2017· Noven Pharmaceuticals, Inc.

Recalled Item: Minivelle (estradiol Transdermal System) 0.1 mg per day Recalled by Noven...

The Issue: Defective Delivery System: Out of specification for peel force from the...

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 26, 2017· Zimmer Biomet, Inc.

Recalled Item: Modular Hybrid Glenoid Base Large for the Comprehensive Shoulder System...

The Issue: Zimmer Biomet is conducting a voluntary recall for a single lot of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2017· Iba Dosimetry

Recalled Item: Large Stealth Chamber Recalled by Iba Dosimetry Due to When the Stealth...

The Issue: When the Stealth Chamber is used as a detector in relative dosimetry,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2017· Stryker Howmedica Osteonics Corp.

Recalled Item: Hoffmann LRF Safety Clip (Bone Transport Strut) Recalled by Stryker...

The Issue: Stryker is recalling Hoffmann LRF (Limb Reconstruction Frame) System Safety...

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

Class II — Potential Health HazardOngoing
FoodApril 26, 2017· Rich Products Corp

Recalled Item: ARTISAN-STYLE PIZZA DOUGH BALL distributed under the following sizes and...

The Issue: The product was made with flour supplied by Ardent Mills who issued a recall...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 26, 2017· Rich Products Corp

Recalled Item: 7 OZ PIZZA DOUGH BALL Recalled by Rich Products Corp Due to Potential E....

The Issue: The product was made with flour supplied by Ardent Mills who issued a recall...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 26, 2017· Rich Products Corp

Recalled Item: ARTISAN CRUST PIZZA DOUGH 24/18 Recalled by Rich Products Corp Due to...

The Issue: The product was made with flour supplied by Ardent Mills who issued a recall...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 25, 2017· Urban Remedy

Recalled Item: Whole Foods Market Cold Pressed Juice Recalled by Urban Remedy Due to...

The Issue: Urban Remedy is voluntarily recalling Non-Dairy Spiced Golden Milk that was...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 25, 2017· Cook Inc.

Recalled Item: Pereyra-Raz Ligature Carrier Recalled by Cook Inc. Due to reprocessing...

The Issue: reprocessing instructions do not provide sufficient detailed information for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2017· Cook Inc.

Recalled Item: Stamey Needle Recalled by Cook Inc. Due to reprocessing instructions do not...

The Issue: reprocessing instructions do not provide sufficient detailed information for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2017· Vascular Solutions, Inc.

Recalled Item: Venture RX Catheter Recalled by Vascular Solutions, Inc. Due to Vascular...

The Issue: Vascular Solutions, Inc. (VSI) is voluntarily removing all lots of Venture...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 25, 2017· Cook Inc.

Recalled Item: Clarke-Reich Laparoscopic Knot Pusher Recalled by Cook Inc. Due to...

The Issue: reprocessing instructions do not provide sufficient detailed information for...

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

Class II — Potential Health HazardOngoing