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 4674146760 of 55,837 recalls

Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Venoatrial Cannulae 36/46 Fr with 1/2" flare or connector Recalled by...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Three-stage Venous Return Cannulae 28 Fr with 3/8" flare Recalled by...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: CPB Catheter Kit Product Usage: Venous Return Cannula is indicated Recalled...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Malleable Venous Return Cannulae 24 Recalled by Terumo Cardiovascular...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Soft-Flow Aortic Cannulae 6.0mm Recalled by Terumo Cardiovascular...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Soft-arc Aortic Cannula 8.0mm curved tip Recalled by Terumo...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo TenderFlow Pediatric Venous Cannulae Recalled by Terumo...

The Issue: During an in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Zimmer, Inc.

Recalled Item: Zimmer M/L Taper Hip Prosthesis with Kinectiv Technology Recalled by Zimmer,...

The Issue: Black residue observed in the sterile pouch of the M/L Taper and Kinectiv stems.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Zimmer, Inc.

Recalled Item: Zimmer M/L Taper Hip Stem Standard & Extended Offset Recalled by Zimmer,...

The Issue: Black residue observed in the sterile pouch of the M/L Taper and Kinectiv stems.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2014· Zimmer, Inc.

Recalled Item: Zimmer M/L Taper Reduced Neck Standard & Extended Offset Recalled by Zimmer,...

The Issue: Black residue observed in the sterile pouch of the M/L Taper and Kinectiv stems.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 5.0mm Acorn Bur Sterile Product Usage: The devices are Recalled by...

The Issue: There may be missing notches, partial notches or no notches at all in some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 5.5mm Round Fluted Bur Soft Touch Sterile Product Usage: Recalled by...

The Issue: There may be missing notches, partial notches or no notches at all in some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 3.0mm x 3.8mm Neuro Drill Less Aggressive Sterile Product Recalled...

The Issue: There may be missing notches, partial notches or no notches at all in some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 5.0mm Round Fluted Bur Aggressive Sterile Product Usage: The...

The Issue: There may be missing notches, partial notches or no notches at all in some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 5.0mm Barrel Bur Sterile Product Usage: The devices are Recalled by...

The Issue: There may be missing notches, partial notches or no notches at all in some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 6.0mm Acorn Bur Sterile Product Usage: The devices are Recalled by...

The Issue: There may be missing notches, partial notches or no notches at all in some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 0.5mm Round Fluted Bur Sterile Product Usage: The devices Recalled...

The Issue: There may be missing notches, partial notches or no notches at all in some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 5.5mm Round Fluted Bur Aggressive Sterile Product Usage: The...

The Issue: There may be missing notches, partial notches or no notches at all in some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Philips Medical Systems, Inc.

Recalled Item: IntelliVue MX40 Wearable Patient Monitor in use with the Philips Recalled by...

The Issue: IntelliVue MX40 (part numbers 865350, 865352) with software revisions B.00...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 22, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker 3.0mm Round Fluted Bur Soft Touch Sterile Product Usage: Recalled by...

The Issue: There may be missing notches, partial notches or no notches at all in some...

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

Class II — Potential Health HazardOngoing