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.

52,339 total recalls
2,582 in last 12 months

Showing 2470124720 of 52,339 recalls

DrugOctober 9, 2018· Sprayology

Recalled Item: SleepEase Recalled by Sprayology Due to CGMP Deviations: products...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2018· Sprayology

Recalled Item: Snore Soother Recalled by Sprayology Due to CGMP Deviations: products...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2018· Sprayology

Recalled Item: Body Balance Recalled by Sprayology Due to CGMP Deviations: products...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2018· Sprayology

Recalled Item: PMS Support Recalled by Sprayology Due to CGMP Deviations: products...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2018· Sprayology

Recalled Item: ImmunoBooster Recalled by Sprayology Due to CGMP Deviations: products...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2018· Sprayology

Recalled Item: Man Power Recalled by Sprayology Due to CGMP Deviations: products...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2018· Sprayology

Recalled Item: Arnica Power Recalled by Sprayology Due to CGMP Deviations: products...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2018· Sprayology

Recalled Item: Bone Builder Recalled by Sprayology Due to CGMP Deviations: products...

The Issue: CGMP Deviations: products manufactured by contract manufacturer under...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2018· Lupin Pharmaceuticals Inc.

Recalled Item: Testosterone Topical Solution Recalled by Lupin Pharmaceuticals Inc. Due to...

The Issue: Defective Container: Repetitive complaints received indicating pump not working.

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 9, 2018· Synaptive Medical Inc

Recalled Item: BrightMatter Guide Recalled by Synaptive Medical Inc Due to This recall has...

The Issue: This recall has been initiated due to a software defect found in the Guide...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 9, 2018· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Fresenius Granuflo Dry Acid Concentrate- 2K 2.0 Ca 1 Mg Recalled by...

The Issue: Discolored powder has confirmed the presence of a foreign substance

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

Class III — Low RiskOngoing
Medical DeviceOctober 9, 2018· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Fresenius Granuflo Dry Acid Concentrate- 2K 2.5 Ca 1 Mg Recalled by...

The Issue: Discolored powder has confirmed the presence of a foreign substance

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

Class III — Low RiskOngoing
Medical DeviceOctober 9, 2018· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Fresenius Granuflo Dry Acid Concentrate- 3K 2.5 Ca 1 Mg Recalled by...

The Issue: Discolored powder has confirmed the presence of a foreign substance

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

Class III — Low RiskOngoing
Medical DeviceOctober 9, 2018· Theragenics Corporation

Recalled Item: Theragenics Applicator Needle (18g x 20cm) The device is comprised Recalled...

The Issue: Some of the pouches containing Brachytherapy Applicator Needles (18g x 20cm)...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2018· Stryker Medical Division of Stryker Corporation

Recalled Item: The Spirit Select Bed Recalled by Stryker Medical Division of Stryker...

The Issue: The beds with the high rail side rail option may not be complaint with IEC...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2018· Stryker Medical Division of Stryker Corporation

Recalled Item: The Spirit Plus Bed Recalled by Stryker Medical Division of Stryker...

The Issue: The beds with the high rail side rail option may not be complaint with IEC...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS¿ Chemistry Products dLDL Reagent-GENs 26 & 27. In Vitro Recalled by...

The Issue: VITROS Chemistry Products dLDL Reagent GENs 26 and 27, negatively biased results

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

Class II — Potential Health HazardOngoing
DrugOctober 8, 2018· ICU Medical Inc

Recalled Item: 5% Dextrose Injection Recalled by ICU Medical Inc Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility; bags have the potential to leak

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 8, 2018· ICU Medical Inc

Recalled Item: 0.9% Sodium Chloride Injection Recalled by ICU Medical Inc Due to Lack of...

The Issue: Lack of Assurance of Sterility; bags have the potential to leak

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 8, 2018· Akorn, Inc.

Recalled Item: Gentamicin Sulfate Ophthalmic Solution Recalled by Akorn, Inc. Due to...

The Issue: Presence of Particulate Matter: Crystalline particles were noticed at the 24...

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

Class II — Potential Health HazardOngoing
Refund