Product Recalls in Alabama

Product recalls affecting Alabama — including food, drugs, consumer products, medical devices, and vehicles distributed to Alabama. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,969 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
1,969 in last 12 months

Showing 1508115100 of 50,591 recalls

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 30, 2021· Philips North America Llc

Recalled Item: Ingenia 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· Philips North America Llc

Recalled Item: Ingenia 1.5T-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· Philips North America Llc

Recalled Item: Ingenia Elition X-Magnetic Resonance Medical Electrical Systems indicated...

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: 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
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· 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· 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· 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
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· Teligent Pharma, Inc.

Recalled Item: Lidocaine Ointment USP Recalled by Teligent Pharma, Inc. Due to Failed...

The Issue: Failed Viscosity Specifications: lot does not meet specification for...

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

Class III — Low RiskOngoing
Refund
DrugJuly 29, 2021· Teligent Pharma, Inc.

Recalled Item: Erythromycin Topical Solution USP Recalled by Teligent Pharma, Inc. Due to...

The Issue: Defective container: possibility for lack of seal integrity.

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: Epoprostenol Sodium for Injection Recalled by Teva Pharmaceuticals USA Due...

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: DAUNOrubicin Hydrochloride Injection 20 mg/4mL 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: 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: Methylprednisolone Acetate Injectable Suspension USP 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: Norepinephrine Bitartrate Injection Recalled by Teva Pharmaceuticals USA Due...

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