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 3024130260 of 52,339 recalls

Medical DeviceMay 19, 2017· GE Healthcare, LLC

Recalled Item: GE Healthcare Optima CT580 Recalled by GE Healthcare, LLC Due to It was...

The Issue: It was discovered that an issue has been identified that can result in a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2017· GE Healthcare, LLC

Recalled Item: GE Healthcare Discovery NM/CT 570c X-ray system Recalled by GE Healthcare,...

The Issue: It was discovered that an issue has been identified that can result in a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2017· Medacta Usa Inc

Recalled Item: Medacta GMK HINGE Recalled by Medacta Usa Inc Due to One lot of product does...

The Issue: One lot of product does not include a screw for attachment to the tibial...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2017· GE Healthcare, LLC

Recalled Item: GE Healthcare LightSpeed VCT X-ray system Recalled by GE Healthcare, LLC Due...

The Issue: It was discovered that an issue has been identified that can result in a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2017· GE Healthcare, LLC

Recalled Item: GE Healthcare Discovery PET/CT 600 Recalled by GE Healthcare, LLC Due to It...

The Issue: It was discovered that an issue has been identified that can result in a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2017· GE Healthcare, LLC

Recalled Item: GE Healthcare Discovery NM/CT 670 CZT X-ray system Recalled by GE...

The Issue: It was discovered that an issue has been identified that can result in a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 19, 2017· GE Healthcare, LLC

Recalled Item: GE Healthcare Discovery NM/CT 670. 670 Pro Recalled by GE Healthcare, LLC...

The Issue: It was discovered that an issue has been identified that can result in a...

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

Class II — Potential Health HazardOngoing
DrugMay 18, 2017· SCA Pharmaceuticals

Recalled Item: ceFAZolin sodium added to 100 mL 0.9% Sodium Chloride injectable Recalled by...

The Issue: Lack of assurance of sterility: Product bags leaking at seam.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 18, 2017· SCA Pharmaceuticals

Recalled Item: fentaNYL (as citrate) in 0.9% Sodium Chloride injectable Recalled by SCA...

The Issue: Lack of assurance of sterility: Product bags leaking at seam.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 18, 2017· SCA Pharmaceuticals

Recalled Item: morphine sulfate in 0.9% Sodium Chloride injectable Recalled by SCA...

The Issue: Lack of assurance of sterility: Product bags leaking at seam.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 18, 2017· SCA Pharmaceuticals

Recalled Item: ceFAZolin sodium added to 100 mL 0.9% Sodium Chloride injectable Recalled by...

The Issue: Lack of assurance of sterility: Product bags leaking at seam.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 18, 2017· SCA Pharmaceuticals

Recalled Item: PHENYLephrine HCL in 0.9% Sodium Chloride injectable Recalled by SCA...

The Issue: Lack of assurance of sterility: Product bags leaking at seam.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 18, 2017· Forest Laboratories, LLC

Recalled Item: Saphris 10 mg (asenapine) sublingual tablets Recalled by Forest...

The Issue: Labeling; Label Mixup; blister lidding foil and shell-pack labeled as 10 mg...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 18, 2017· SCA Pharmaceuticals

Recalled Item: fentaNYL (as citrate) in 100mL 0.9% Sodium Chloride injectable Recalled by...

The Issue: Lack of assurance of sterility: Product bags leaking at seam.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 18, 2017· SCA Pharmaceuticals

Recalled Item: fentaNYL (as citrate) in 0.9% Sodium Chloride injectable Recalled by SCA...

The Issue: Lack of assurance of sterility: Product bags leaking at seam.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 18, 2017· SCA Pharmaceuticals

Recalled Item: morphine sulfate in 0.9% Sodium Chloride injectable Recalled by SCA...

The Issue: Lack of assurance of sterility: Product bags leaking at seam.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 18, 2017· SCA Pharmaceuticals

Recalled Item: HYDROmorphone HCL in 0.9% Sodium Chloride injectable Recalled by SCA...

The Issue: Lack of assurance of sterility: Product bags leaking at seam.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 18, 2017· SCA Pharmaceuticals

Recalled Item: MAGNESIUM Sulfate added to 100 mL 0.9% Sodium Chloride injectable Recalled...

The Issue: Lack of assurance of sterility: Product bags leaking at seam.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 18, 2017· Hospira Inc., A Pfizer Company

Recalled Item: Levophed norepinephrine bitartrate Recalled by Hospira Inc., A Pfizer...

The Issue: GMP Deviation; A foreign stopper was observed during packaging of a lot of...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 18, 2017· Correctional Industries Food Factory

Recalled Item: Item 10075 - WHITE WHOLE WHEAT BREAD SLICES Recalled by Correctional...

The Issue: Product is recalled because it was made with water contaminated with...

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

Class III — Low RiskOngoing
Refund