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. 1,948 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
1,948 in last 12 months

Showing 2802128040 of 55,837 recalls

Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost Recalled by Philips Medical Systems Gmbh, DMC Due to The...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712082 Recalled by...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost Release 3.1 (Stitching Patient Support) 712026 Recalled by...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· bioMerieux, Inc.

Recalled Item: BACT/ALERT VIRTUO system Recalled by bioMerieux, Inc. Due to The BACT/ALERT...

The Issue: The BACT/ALERT VIRTUO Instrument Firmware version R2.0 allows relocation of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· bioMerieux, Inc.

Recalled Item: BACT/ALERT VIRTUO system Recalled by bioMerieux, Inc. Due to The BACT/ALERT...

The Issue: The BACT/ALERT VIRTUO Instrument Firmware version R2.0 allows relocation of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost Release 3 (Stitching Patient Support) 712025 Recalled by...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost Recalled by Philips Medical Systems Gmbh, DMC Due to The...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost 4 Chest / Emergency (Stitching Patient Support) 712029...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost 4 High Performance (Stitching Patient Support) 712027...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: EasyDiagnost Eleva DRF Recalled by Philips Medical Systems Gmbh, DMC Due to...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost 4.1 (Stitching Patient Support) 712225 Recalled by Philips...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost Classic 1.x Upgrades (Stitching Patient Support) 712081...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost 4.1 Flex / Value (Stitching Patient Support) 712028 Recalled...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: CombiDiagnost R90 (Stitching Patient Support) 709030 Recalled by Philips...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost Release 3.1 (Stitching Patient Support) 712026 Recalled by...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost Classic Recalled by Philips Medical Systems Gmbh, DMC Due to...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost 4 Flex / Value (Stitching Patient Support) 712028 Recalled...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost Dual Detector (Stitching Patient Support) 712022 Recalled by...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost Single Detector (Stitching Patient Support) 712020 Recalled...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost 4.1 High Performance (Stitching Patient Support) 712031...

The Issue: The hook does not securely hold the footplate in the vertical position....

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

Class II — Potential Health HazardOngoing