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 3022130240 of 55,837 recalls

DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Human Chorionic Gonadotropin 20 Recalled by KRS Global Biotechnology, Inc...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Human Chorionic Gonadotropin 5 Recalled by KRS Global Biotechnology, Inc Due...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Sermorelin Recalled by KRS Global Biotechnology, Inc Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: 7-Keto DHEA 25mg Capsule Recalled by KRS Global Biotechnology, Inc Due to...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Vitamin 10 B Lyophilized Vial Recalled by KRS Global Biotechnology, Inc Due...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Human Chorionic Gonadotropin 11 Recalled by KRS Global Biotechnology, Inc...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Amphotericin 60 mg/Chloramphenicol 600 mg/Hydrocortisone 10 mg Otic Powder...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Sincalide 5 mcg Lyophilized Vials Recalled by KRS Global Biotechnology, Inc...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 15, 2017· Cordis Corporation

Recalled Item: Cordis S.M.A.R.T. Flex Biliary Stent System Product Usage: Is indicated...

The Issue: Potential for cracked luer hubs

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2017· Implant Direct Sybron Manufacturing, LLC

Recalled Item: Spectra System/Legacy Guided Surgery Handle Kit (Part Number: G-HK) Spectra...

The Issue: The Spectra System/Legacy Guided Surgery Handle Kit had guided handle...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with...

The Issue: Products do not contain the Central Venous Catheter Placement Procedures...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Multi- Lumen CVC Kit Recalled by Arrow International Inc...

The Issue: Products do not contain the Central Venous Catheter Placement Procedures...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2017· Alere San Diego, Inc.

Recalled Item: Triage Drugs of Abuse Plus TCA 25 Test Kit Recalled by Alere San Diego, Inc....

The Issue: The recalled lots have demonstrated unexpected false positive THC results.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2017· Arrow International Inc

Recalled Item: ARROWg+ard Blue PLUS Pressure Injectable Multi-Lumen CVC Kit. Intended to...

The Issue: Products do not contain the Central Venous Catheter Placement Procedures...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2017· Carl Zeiss Metrology Inc

Recalled Item: Metrotom 800 (130kV CT scanner) Industrial CT scanner for measuring Recalled...

The Issue: Due to a software error, it was observed that when the user closes the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2017· Arrow International Inc

Recalled Item: Percutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port...

The Issue: Products do not contain the Central Venous Catheter Placement Procedures...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2017· Arrow International Inc

Recalled Item: Percutaneous Sheath Introducer Kit with ARROWg+ard Blue Sheath Recalled by...

The Issue: Products do not contain the Central Venous Catheter Placement Procedures...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with...

The Issue: Products do not contain the Central Venous Catheter Placement Procedures...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Two- Lumen Central Venous Catheterization Kit with Blue...

The Issue: Products do not contain the Central Venous Catheter Placement Procedures...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2017· Arrow International Inc

Recalled Item: Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with...

The Issue: Products do not contain the Central Venous Catheter Placement Procedures...

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

Class II — Potential Health HazardOngoing