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. 1,091 recalls have been distributed to Arizona in the last 12 months.

52,339 total recalls
1,091 in last 12 months

Showing 15441–15460 of 52,339 recalls

Medical DeviceJuly 30, 2021· Philips North America Llc

Recalled Item: Achieva 3.0T-Magnetic Resonance Medical Electrical Systems indicated for use...

The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2021· Leica Microsystems, Inc.

Recalled Item: BOND Ready-To-Use Primary Antibody CDX2 (EP25) Recalled by Leica...

The Issue: Product may not perform as specified in IFU.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 30, 2021· Philips North America Llc

Recalled Item: Ingenia 1.5T Evoluton- Magnetic Resonance Medical Electrical Systems...

The Issue: Pressure relief valve 42 psi installed in the magnet assembly instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2021· Hitachi Healthcare Americas Corporation

Recalled Item: ECHELON Oval MRI System Recalled by Hitachi Healthcare Americas Corporation...

The Issue: There was no label on the pad packaging or notification in the user manual...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2021· Sentinel CH SpA

Recalled Item: Alinity c CRP Vario Cardiac High Sensitivity Calibrator Kit ( by Sentinel CH...

The Issue: Calibrator vials were incorrectly labeled. Use of incorrectly labeled vials...

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

Class III — Low RiskOngoing
Medical DeviceJuly 29, 2021· Lymol Medical Corporation

Recalled Item: LYMOL Medical Elite X Class Rigid Bronchoscope System Recalled by Lymol...

The Issue: Reprocessing instructions were revised November 15, 2020, to new processes...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2021· Hitachi Healthcare Americas Corporation

Recalled Item: ECHELON MRI System Recalled by Hitachi Healthcare Americas Corporation Due...

The Issue: There was no label on the pad packaging or notification in the user manual...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2021· Mizuho OSI

Recalled Item: HANA/PROFx CLASSIC FEMORAL HOOK RIGHT Recalled by Mizuho OSI Due to One...

The Issue: One batch of "regular" femoral hooks were incorrectly etched with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 29, 2021· Hitachi Healthcare Americas Corporation

Recalled Item: OASIS MRI System Recalled by Hitachi Healthcare Americas Corporation Due to...

The Issue: There was no label on the pad packaging or notification in the user manual...

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

Class II — Potential Health HazardOngoing
DrugJuly 29, 2021· PAI Holdings, LLC. dba Pharmaceutical Associates Inc

Recalled Item: Cimetidine Hydrochloride Oral Solution 300 mg/5 mL Recalled by PAI Holdings,...

The Issue: Lack of CGMP: This recall is being carried out due to potential for carry...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2021· Teva Pharmaceuticals USA

Recalled Item: Cyclobenzaprine Hydrochloride Tablets Recalled by Teva Pharmaceuticals USA...

The Issue: CGMP Deviations: Out of specification (OOS) test result for Total Aerobic...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2021· PAI Holdings, LLC. dba Pharmaceutical Associates Inc

Recalled Item: Ethosuximide Oral Solution USP 250 mg/5 mL Recalled by PAI Holdings, LLC....

The Issue: Lack of CGMP: This recall is being carried out due to potential for carry...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2021· Teva Pharmaceuticals USA

Recalled Item: Adenosine Injection Recalled by Teva Pharmaceuticals USA Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2021· Teva Pharmaceuticals USA

Recalled Item: Vecuronium Bromide for Injection 10 mg Recalled by Teva Pharmaceuticals USA...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2021· Teva Pharmaceuticals USA

Recalled Item: Metoclopramide Injection USP Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2021· Teva Pharmaceuticals USA

Recalled Item: Alprostadil Injection USP Recalled by Teva Pharmaceuticals USA Due to Lack...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2021· Teva Pharmaceuticals USA

Recalled Item: Amikacin Sulfate Injection USP 1 gram/4mL (250mg/ML) Recalled by Teva...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2021· Teva Pharmaceuticals USA

Recalled Item: Adenosine Injection Recalled by Teva Pharmaceuticals USA Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2021· Teva Pharmaceuticals USA

Recalled Item: Leucovorin Calcium for Injection Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 29, 2021· Teva Pharmaceuticals USA

Recalled Item: Haloperidol Decanoate Injection 100 mg/mL Recalled by Teva Pharmaceuticals...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund