Product Recalls in Florida

Product recalls affecting Florida — including food, drugs, consumer products, medical devices, and vehicles distributed to Florida. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,815 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,815 in last 12 months

Showing 1708117100 of 30,686 recalls

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
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: 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
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: 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: Tibial 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: 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