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.
Showing 30941–30960 of 52,339 recalls
Recalled Item: 30 count Miss Vickies Multipack Tray 41.25 oz. packaged in flexible plastic...
The Issue: Potential presence of Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Microfil Composite Instruments are packaged in an unsealed plastic sleeve...
The Issue: Microfil Composite Instruments were distributed with a sterile symbol on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Positive Susceptibility card (AST-P603) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Positive Susceptibility card (AST-P629) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Acumed Slide-Loc Anatomic Radial Head System is intended for Recalled by...
The Issue: The firm initiates a voluntary removal and discontinue marketing of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10-1335M - SpF-XL IIB 2/DM Implantable Stimulator. Indicated as a Recalled...
The Issue: Zimmer Biomet is conducting a medical device field action for the SpF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N350) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N211) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10-1398M - SpF-PLUS Implantable Stimulator. Indicated as a spinal fusion...
The Issue: Zimmer Biomet is conducting a medical device field action for the SpF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N293) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phenobarbital Tablets USP Recalled by C. O. Truxton Due to Mislabeling
The Issue: Labeling: Label Mixup; potentially mislabeled
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IC-Green (indocyanine green for injection Recalled by Akorn, Inc. Due to...
The Issue: Product is being recalled due to low pH value.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenobarbital Tablets USP Recalled by C. O. Truxton Due to Mislabeling
The Issue: Labeling: Label Mixup; potentially mislabeled
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenobarbital Tablets USP Recalled by C. O. Truxton Due to Mislabeling
The Issue: Labeling: Label Mixup; potentially mislabeled
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenobarbital Tablets USP Recalled by C. O. Truxton Due to Labeling: Labeled...
The Issue: Labeling: Labeled Error on Declared Strength; report of a 1000 ct bottle...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amitriptyline HCL Tablets Recalled by C. O. Truxton Due to Mislabeling
The Issue: Labeling: Label Mixup; potentially mislabeled
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenobarbital Tablets USP Recalled by C. O. Truxton Due to Mislabeling
The Issue: Labeling: Label Mixup; potentially mislabeled
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-GN92) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N334) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N314) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.