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. 2,478 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,478 in last 12 months

Showing 2636126380 of 50,591 recalls

Medical DeviceMay 1, 2018· TP Orthodontics, Inc.

Recalled Item: Jasper Vektor Recalled by TP Orthodontics, Inc. Due to The firm has received...

The Issue: The firm has received 106 complaints of the device breaking in the patient's...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· TP Orthodontics, Inc.

Recalled Item: Jasper Vektor Recalled by TP Orthodontics, Inc. Due to The firm has received...

The Issue: The firm has received 106 complaints of the device breaking in the patient's...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· TP Orthodontics, Inc.

Recalled Item: Jasper Vektor Recalled by TP Orthodontics, Inc. Due to The firm has received...

The Issue: The firm has received 106 complaints of the device breaking in the patient's...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· TP Orthodontics, Inc.

Recalled Item: Jasper Vektor Recalled by TP Orthodontics, Inc. Due to The firm has received...

The Issue: The firm has received 106 complaints of the device breaking in the patient's...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· TP Orthodontics, Inc.

Recalled Item: Jasper Vektor Recalled by TP Orthodontics, Inc. Due to The firm has received...

The Issue: The firm has received 106 complaints of the device breaking in the patient's...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· TP Orthodontics, Inc.

Recalled Item: Jasper Vektor Recalled by TP Orthodontics, Inc. Due to The firm has received...

The Issue: The firm has received 106 complaints of the device breaking in the patient's...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· TP Orthodontics, Inc.

Recalled Item: Jasper Vektor Recalled by TP Orthodontics, Inc. Due to The firm has received...

The Issue: The firm has received 106 complaints of the device breaking in the patient's...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2018· Philips Electronics North America Corporation

Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...

The Issue: Five warning statements are missing from the instructions for use.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2018· Philips Electronics North America Corporation

Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...

The Issue: Five warning statements are missing from the instructions for use.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2018· Philips Electronics North America Corporation

Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...

The Issue: Five warning statements are missing from the instructions for use.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2018· Philips Electronics North America Corporation

Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...

The Issue: Five warning statements are missing from the instructions for use.

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

Class II — Potential Health HazardOngoing
DrugApril 27, 2018· Sanofi-Aventis U.S. LLC

Recalled Item: Docetaxel injection concentrate Recalled by Sanofi-Aventis U.S. LLC Due to...

The Issue: Superpotent drug: over-concentrated vials of Docetaxel injection concentrate...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 27, 2018· GE Healthcare Japan Corporation

Recalled Item: GE Healthcare Revolution EVO Recalled by GE Healthcare Japan Corporation Due...

The Issue: GE Healthcare has identified that some CT systems may have a damaged cable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2018· GE Healthcare Japan Corporation

Recalled Item: GE Healthcare Optima CT660. The systems are intended for head Recalled by GE...

The Issue: GE Healthcare has identified that some CT systems may have a damaged cable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2018· GE Healthcare Japan Corporation

Recalled Item: GE Healthcare Optima CT660. Sold under the following product names: Recalled...

The Issue: GE Healthcare has identified that some CT systems may have a damaged cable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2018· GE Healthcare Japan Corporation

Recalled Item: GE Healthcare Optima CT540. The systems are intended for head Recalled by GE...

The Issue: GE Healthcare has identified that some CT systems may have a damaged cable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2018· Stryker GmbH

Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...

The Issue: The manufacturer has discovered that potentially out-of-specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2018· Stryker GmbH

Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...

The Issue: The manufacturer has discovered that potentially out-of-specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2018· Stryker GmbH

Recalled Item: Ankle Arthrodesis Nail Recalled by Stryker GmbH Due to The manufacturer has...

The Issue: The manufacturer has discovered that potentially out-of-specification...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2018· Stryker GmbH

Recalled Item: Femoral Nail Recalled by Stryker GmbH Due to The manufacturer has discovered...

The Issue: The manufacturer has discovered that potentially out-of-specification...

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

Class II — Potential Health HazardOngoing