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. 2,710 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,710 in last 12 months

Showing 2548125500 of 30,686 recalls

Medical DeviceSeptember 15, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur¿ Systems HBc Total (HBcT) Recalled by Siemens...

The Issue: Increased imprecision and positive bias is observed with patient samples and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2014· Codman & Shurtleff, Inc.

Recalled Item: Codman Lumbar Drainage Catheter Kit II with EDS 3 (External Recalled by...

The Issue: tubing within the system that drains CSF may leak or disconnect from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2014· Codman & Shurtleff, Inc.

Recalled Item: Codman EDS 3 Drainage System (no Ventricular Catheter) (External Drainage...

The Issue: tubing within the system that drains CSF may leak or disconnect from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2014· Codman & Shurtleff, Inc.

Recalled Item: Codman EDS 3 Drainage System with Ventricular Catheter (External Drainage...

The Issue: tubing within the system that drains CSF may leak or disconnect from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿¿ Systems HBc Total (HBcT) Kit. For In Vitro Recalled by...

The Issue: Increased imprecision and positive bias is observed with patient samples and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2014· Invivo Corporation

Recalled Item: Philips Expression Information Portal (IP5) Model 865471. The IP5 is...

The Issue: Frozen Display Numerics and Disabled Menu Keys after extended run time. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2014· Eyemart Express Ltd

Recalled Item: Prescription eyeglass safety lenses. Vision correction Recalled by Eyemart...

The Issue: Prescription eyeglass safety lenses did not meet specifications.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: Omni Micro-electrode/ electrode for cobas b221 analyzer. The Roche...

The Issue: The default for normal values are inconsistent between cobas b 221 and other...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 12, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur¿ and ADVIA Centaur¿ XP and ADVIA Centaur¿ CP Recalled by...

The Issue: Stability of the ADVIA Centaur Cleaning Solution is not assured

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

Class III — Low RiskOngoing
Medical DeviceSeptember 11, 2014· Abbott Ireland Diagnostics Division

Recalled Item: ARCHITECT Total T3 Reagent Kit (7K64) consists of: - 1 Recalled by Abbott...

The Issue: 17% of ARCHITECT Total T3 Reagent Kit, LN 7K64-20/-25 reagent lots 38901UI00...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2014· Intuitive Surgical, Inc.

Recalled Item: ASSEMBLY Recalled by Intuitive Surgical, Inc. Due to Correction due to the...

The Issue: Correction due to the detection of a motor sensor failure in the Patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2014· Philips Medical Systems (Cleveland) Inc

Recalled Item: The Ingenuity CT Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: Ingenuity CT system can mislabel the exposure that results in an image in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2014· The Binding Site Group, Ltd.

Recalled Item: Human lgG Subclass Liquid Reagent Kits for use on the Recalled by The...

The Issue: Customer complaints identified that samples containing extremely high IgG4...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2014· The Binding Site Group, Ltd.

Recalled Item: Human lgG4 Subclass Liquid Reagent Kits for use on the Recalled by The...

The Issue: Customer complaints identified that samples containing extremely high IgG4...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2014· The Binding Site Group, Ltd.

Recalled Item: Human lgG4 Subclass kit for use on the Beckman Coulter Recalled by The...

The Issue: Customer complaints identified that samples containing extremely high IgG4...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2014· The Binding Site Group, Ltd.

Recalled Item: Human lgG4 Subclass Liquid Reagent Kits Human lgG1& lgG2 Antisera Recalled...

The Issue: Customer complaints identified that samples containing extremely high IgG4...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2014· The Binding Site Group, Ltd.

Recalled Item: MininephThl Human lgG4 Kit Product Code: ZK009.LR This kit is Recalled by...

The Issue: Customer complaints identified that samples containing extremely high IgG4...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2014· The Binding Site Group, Ltd.

Recalled Item: Human lgG4 Subclass Liquid Reagent Kits For use on the Recalled by The...

The Issue: Customer complaints identified that samples containing extremely high IgG4...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2014· The Binding Site Group, Ltd.

Recalled Item: Human Subclass Kit for use on the Beckman IMMAGE"/IMMAGE"800 Analyser...

The Issue: Customer complaints identified that samples containing extremely high IgG4...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2014· Zimmer, Inc.

Recalled Item: Persona The Personalized Knee System 2.5 mm Female Screw 48 Recalled by...

The Issue: The Persona 48mm X 2.5mm Female Screw is being recalled due to potential use...

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

Class II — Potential Health HazardOngoing