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 2950129520 of 30,686 recalls

Medical DeviceSeptember 18, 2012· Instratek, Incorporated

Recalled Item: Endotrig Trigger Release Sterile Micro Hook Blade Product Usage: The...

The Issue: Instratek, Inc.has received multiple complaints of the 1052 Trigger Finger...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2012· Trophy Sas

Recalled Item: CareStream Dental Kodak 2100 Intraoral X-ray system Product Usage: The...

The Issue: There have been approximately 2% of the x-ray generators manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2012· Philips Medical Systems (Cleveland) Inc

Recalled Item: Mx8000 IDT Whole Body Computed Tomography X-ray system Distributed by...

The Issue: The low contrast pins in the Image Quality (IQ) phantom deteriorates over...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2012· Elekta, Inc.

Recalled Item: MOSAIQ MOSAIQ is an image-enabled electronic medical record system (EMR)...

The Issue: A patient was seriously mistreated after a user made and saved an...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint¿ 500 system blood gas analyzer Product Usage: RAPIDPoint...

The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDLab¿ 1265 system blood gas analyzer Product Usage: RAPIDLab...

The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint¿¿ 405 system blood gas analyzer Product PUsage: These...

The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDLab¿ 1240 system blood gas analyzer Product Usage: RAPIDLab...

The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDLab¿ 1245 system blood gas analyzer Product Usage: RAPIDLab...

The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint¿ 400 system blood gas analyzer Product Usage: These...

The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2012· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDLab¿ 1260 system blood gas analyzer Product Usage: RAPIDLab...

The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2012· KCI USA, Inc.

Recalled Item: BariAir Therapy System The BariAir Therapy System is a risk Recalled by KCI...

The Issue: KCI has issued a medical device correction for the BariAir Therapy System...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2012· Ge Healthcare It

Recalled Item: Centricity PACS System versions 3.X and higher and 4.X and Recalled by Ge...

The Issue: There is a potential loss of image(s) associated with the Centricity to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2012· Sorin Group USA, Inc.

Recalled Item: Gish 3/8 x 1/2" Reducer Connector with Luer fitting Recalled by Sorin Group...

The Issue: Due to a molding irregularity, certain lots of connectors have the potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2012· Hologic, Inc.

Recalled Item: Hologic Fluoroscan Mini C-Arm Model with InSight- FD Software Version...

The Issue: Fluoroscan Mini C-Arm models -InSight2, version 4.0 and 4.0.1 - DICOM images...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2012· Zimmer, Inc.

Recalled Item: Trilogy F/M Acetabular Shell without holes. Several ODs: 40MM Recalled by...

The Issue: Some units of Trilogy shells manufactured since March 2009 may be below the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2012· Zimmer, Inc.

Recalled Item: Trilogy Acetabular Shell Spiked. The Trilogy Acetabular System is indicated...

The Issue: Some units of Trilogy shells manufactured since March 2009 may be below the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2012· Sorin Group USA, Inc.

Recalled Item: Gish 3/8 x 3/8" Straight Connector with Luer fitting Recalled by Sorin Group...

The Issue: Due to a molding irregularity, certain lots of connectors have the potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2012· Zimmer, Inc.

Recalled Item: Trilogy Acetabular AB Shells with Cluster Holes. The Trilogy Acetabular...

The Issue: Some units of Trilogy shells manufactured since March 2009 may be below the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2012· Zimmer, Inc.

Recalled Item: Trilogy Acetabular Shells with Holes. The Trilogy Acetabular System is...

The Issue: Some units of Trilogy shells manufactured since March 2009 may be below the...

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

Class II — Potential Health HazardOngoing