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. 2,754 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,754 in last 12 months

Showing 2062120640 of 30,686 recalls

Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: 12.4cm Heavy Duty Long Heavy Short Attachment Product Usage: Pneumatic...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: eMax2 PLUS Product Usage: Electric system Recalled by The Anspach Effort,...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: Autolube-III with 20ft hose Product Usage: Pneumatic system Recalled by The...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: Bearing Sleeve Recalled by The Anspach Effort, Inc. Due to Supplied...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: 26.65CM ATTACHMENT Recalled by The Anspach Effort, Inc. Due to Supplied...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: 13.5CM ANGLE ATTACHMENT Recalled by The Anspach Effort, Inc. Due to Supplied...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: 8cm QD Angle Attachment Recalled by The Anspach Effort, Inc. Due to Supplied...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: Large Craniotome Product Usage: Pneumatic system Recalled by The Anspach...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: 5.0cm Short Attachment Recalled by The Anspach Effort, Inc. Due to Supplied...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: Autolube-III with Irrigation Product Usage: Pneumatic system Recalled by The...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: 11.0cm Long Attachment Product Usage: Pneumatic system Recalled by The...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: Autolube-III with Foot Guard Product Usage: Pneumatic system Recalled by The...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: 19cm Attachment Recalled by The Anspach Effort, Inc. Due to Supplied...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: Foot control irrigation system Product Usage: Pneumatic system Recalled by...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: 45 degree Contra Angle Attachment Product Usage: Pneumatic system Recalled...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: 90 degree Contra Angle Attachment Product Usage: Pneumatic system Recalled...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: IMRI SHORT ATTACHMENT Product Usage: Pneumatic system Recalled by The...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: Bearing Sleeve Recalled by The Anspach Effort, Inc. Due to Supplied...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: BLACKMAX-NEURO LOW PRESSURE Product Usage: Pneumatic system Recalled by The...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: Rotating Large Craniotome Recalled by The Anspach Effort, Inc. Due to...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing