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. 2,615 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,615 in last 12 months

Showing 5266152680 of 55,837 recalls

DrugFebruary 1, 2013· Fresenius Kabi USA LLC (FK USA)

Recalled Item: CALCIUM GLUCONATE INJECTION Recalled by Fresenius Kabi USA LLC (FK USA) Due...

The Issue: Labeling: Missing label

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

Class III — Low RiskOngoing
Refund
FoodFebruary 1, 2013· GoldCoast Salads

Recalled Item: GoldCoast Salads Smoked Salmon Spread (8oz and 16oz in flexible Recalled by...

The Issue: Product may be contaminated with Listeria Monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 1, 2013· GoldCoast Salads

Recalled Item: GoldCoast Salads Marine Lobster Spread (8oz and 16oz in flexible Recalled by...

The Issue: Product may be contaminated with Listeria Monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 1, 2013· GoldCoast Salads

Recalled Item: GoldCoast Salads Lobster & Shrimp Spread (8oz and 16oz in Recalled by...

The Issue: Product may be contaminated with Listeria Monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 1, 2013· GoldCoast Salads

Recalled Item: GoldCoast Salads Blue Crab Spread (8oz and 16oz in flexible Recalled by...

The Issue: Product may be contaminated with Listeria Monocytogenes

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+ Hyperbaric Infusion System is a cassette based Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+3 Infusion System is a cassette based multifunction Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+3 Infusion System is a cassette based multifunction Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+ Infusion System is a cassette based multifunction Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+3 Infusion System is a cassette based multifunction Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+ Infusion System is a cassette based multifunction Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing