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. 2,670 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
2,670 in last 12 months

Showing 3842138440 of 55,837 recalls

Medical DeviceMarch 3, 2016· Roche Molecular Systems, Inc.

Recalled Item: Hand-Held Scanner USB IT3800 For sample identification and tracking when...

The Issue: The hand-held barcode scanner model IT3800 used with the COBAS AmpliPrep...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Kerlix X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Curity X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· ArthroCare Corporation

Recalled Item: TOPAZ MicroDebrider 0.8 mm Recalled by ArthroCare Corporation Due to During...

The Issue: During functional testing of devices after real time aging, it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Curity X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Kerlix" X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Curity All Purpose Sponges Recalled by Covidien LLC Due to Compromised...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Curity X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Curity X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Vistec X-Ray Detectable Sponges Recalled by Covidien LLC Due to Compromised...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Curity X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Vistec X-Ray Detectable Sponges Recalled by Covidien LLC Due to Compromised...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Kerlix" X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Curity" X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Dynarex Corporation

Recalled Item: dynarex Specimen Containers Recalled by Dynarex Corporation Due to Exterior...

The Issue: Exterior carton is mis-labeled as Sterile. Non-sterile, bulk specimen...

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

Class II — Potential Health HazardOngoing
DrugMarch 3, 2016· Dr. Reddy's Laboratories, Inc.

Recalled Item: Zoledronic Acid Injection Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Lack of Assurance of Sterility; defective seals where the metal silver ring...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 2, 2016· GE Inspection Technologies, LP

Recalled Item: GE Inspection Technologies Recalled by GE Inspection Technologies, LP Due to...

The Issue: Radiation emissions which exceeded the limit in the performance standard...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc...

The Issue: Software bugs in these SOMATOM systems could possibly cause scan aborts,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA,...

The Issue: Software bugs in these SOMATOM systems could possibly cause scan aborts,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens SOMATOM Definition Recalled by Siemens Medical Solutions USA, Inc...

The Issue: Software bugs in these SOMATOM systems could possibly cause scan aborts,...

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

Class II — Potential Health HazardOngoing