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. 1,819 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
1,819 in last 12 months

Showing 4554145560 of 55,837 recalls

Medical DeviceNovember 4, 2014· Aircraft Medical Limited

Recalled Item: McGrath MAC2 Video Laryngoscope Blades Product supplied in box of 50 items...

The Issue: The blade retaining clip may be difficult to engage and thereby increase the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2014· Smith & Nephew, Inc.

Recalled Item: LEGION(TM) COCR CONSTRAINED FEMORAL COMPONENT Recalled by Smith & Nephew,...

The Issue: The stem taper on this device is undersized; the gauge point is not deep enough.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2014· Smith & Nephew, Inc.

Recalled Item: LEGION(TM) COCR CONSTRAINED FEMORAL COMPONENT Recalled by Smith & Nephew,...

The Issue: The stem taper on this device is undersized; the gauge point is not deep enough.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2014· Medtronic MiniMed Inc.

Recalled Item: Medtronic MiniMed Silhouette and/or MiniMed Sure-T Infusion Sets Recalled by...

The Issue: Tubing may detach at the connect/disconnect location on the MiniMed...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2014· Smith & Nephew, Inc.

Recalled Item: LEGION(TM) COCR CONSTRAINED FEMORAL COMPONENT Recalled by Smith & Nephew,...

The Issue: The stem taper on this device is undersized; the gauge point is not deep enough.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2014· Pulsion Medical Inc

Recalled Item: Pulsiocath PiCCO ProAQT Monitoring Kit Recalled by Pulsion Medical Inc Due...

The Issue: Internal testing and investigation of the packaging revealed cracks and...

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

Class II — Potential Health HazardOngoing
FoodNovember 4, 2014· R and S Gourmet Warehouse

Recalled Item: Gourmet Warehouse Recalled by R and S Gourmet Warehouse Due to Undeclared Non

The Issue: Undeclared non-allergens, soy, wheat, anchovies.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodNovember 4, 2014· International Sprout Holding Inc.

Recalled Item: Alfalfa Seed in plastic lined bags labeled in part *** VNS Alfalfa Recalled...

The Issue: A sample of one lot of product tested positive for salmonella.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodNovember 4, 2014· R and S Gourmet Warehouse

Recalled Item: Gourmet Warehouse Recalled by R and S Gourmet Warehouse Due to Undeclared Non

The Issue: Undeclared non-allergens, soy, wheat, anchovies.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM MONOPOLAR CURVED SCISSORS Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM FENESTRATED BIPOLAR FORCEPS Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2014· Intuitive Surgical, Inc.

Recalled Item: 8MM Recalled by Intuitive Surgical, Inc. Due to Deviations in reprocessing...

The Issue: Deviations in reprocessing steps from those stated in the reprocessing...

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

Class II — Potential Health HazardOngoing