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. 2,582 recalls have been distributed to Arizona in the last 12 months.
Showing 24481–24500 of 52,339 recalls
Recalled Item: STEPHANIX D2RS Digital Dynamic Remote...
The Issue: The firm has detected a potential risk using the command. After releasing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curaplex Epi Kit NOT FOR IV USE Recalled by Bound Tree Medical, LLC Due to...
The Issue: Labeling Incorrect Instructions: This recall has been initiated because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Isosorbide Dinitrate Tablets Recalled by Sandoz Inc Due to Cross...
The Issue: Cross Contamination with Other Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Isosorbide Dinitrate Tablets Recalled by Sandoz Inc Due to Cross...
The Issue: Cross Contamination with Other Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Isosorbide Dinitrate Tablets Recalled by Sandoz Inc Due to Cross...
The Issue: Cross Contamination with Other Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: curaplex Epi Safe Administration and Training Kits Recalled by Bound Tree...
The Issue: Labeling Incorrect Instructions: This recall has been initiated because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: curaplex Epi Safe Kit Recalled by Bound Tree Medical, LLC Due to Labeling...
The Issue: Labeling Incorrect Instructions: This recall has been initiated because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Curaplex Epi Safe Kit Recalled by Bound Tree Medical, LLC Due to Labeling...
The Issue: Labeling Incorrect Instructions: This recall has been initiated because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Isosorbide Dinitrate Tablets Recalled by Sandoz Inc Due to Cross...
The Issue: Cross Contamination with Other Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nitrofurantoin Capsules Recalled by Sandoz Inc Due to Cross Contamination...
The Issue: Cross Contamination with Other Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nitrofurantoin Capsules Recalled by Sandoz Inc Due to Cross Contamination...
The Issue: Cross Contamination with Other Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Curaplex Epi Safe Kit Recalled by Bound Tree Medical, LLC Due to Labeling:...
The Issue: Labeling: Incorrect or missing Lot and/or Exp Date:The Kit is incorrectly...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: curaplex Epi Safe Administration and Training Kits # 8600-01100. Kit...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp date: vials of epinephrine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Genesys Analytical Column Recalled by Clark Laboratories, Inc. (dba,Trinity...
The Issue: lack of 510K
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ultra2 Genesys Variants Analyzer Recalled by Clark Laboratories, Inc....
The Issue: lack of 510K
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesys Diluent Reagent Recalled by Clark Laboratories, Inc. (dba,Trinity...
The Issue: lack of 510K
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The SQ-RX Pulse Generator a component of the Subcutaneous Implantable...
The Issue: Experienced accelerated battery depletion and a shortened replacement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS NT-proBNP Reagent Recalled by ORTHO-CLINICAL DIAGNOSTICS Due to The...
The Issue: The firm is extending their previous July 2018 recall to include additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesys 1 Reagent Recalled by Clark Laboratories, Inc. (dba,Trinity Biotech...
The Issue: lack of 510K
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS HBeAg Reagent Recalled by ORTHO-CLINICAL DIAGNOSTICS Due to The firm...
The Issue: The firm is extending their previous July 2018 recall to include additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.