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. 1,132 recalls have been distributed to Florida in the last 12 months.

55,837 total recalls
1,132 in last 12 months

Showing 14141–14160 of 55,837 recalls

Medical DeviceFebruary 25, 2022· CELLTRION USA INC

Recalled Item: Celltrion DiaTrust COVID-19 Ag Rapid Test Recalled by CELLTRION USA INC Due...

The Issue: Kits were labeled with incorrect expiration dates.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: Total Knee Pack - Surgical Kit Recalled by Stradis Medical, LLC dba Stradis...

The Issue: The outer bag may be perforated or torn, which may result in a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis icono biplane- in combination with a Siemens Healthineers table...

The Issue: Five potential software issues affecting Artis pheno and Artis icono systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2022· Microbiologics Inc

Recalled Item: Mycoplasma genitalium Control Panel (Inactivated Pellet) Recalled by...

The Issue: Distributed product did not undergo proper release testing.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: Anterior Hip Pack - Surgical Kit Recalled by Stradis Medical, LLC dba...

The Issue: The outer bag may be perforated or torn, which may result in a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2022· Philips North America Llc

Recalled Item: DigitalDiagnost C50 1.1 Recalled by Philips North America Llc Due to...

The Issue: Following a system restart where the Table Height 2 (TH2) is the default...

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

Class II — Potential Health HazardOngoing
DrugFebruary 25, 2022· B. Braun Medical, Inc.

Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by B. Braun Medical, Inc. Due to...

The Issue: Lack of sterility assurance: leaking bags

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 24, 2022· The Harvard Drug Group

Recalled Item: hydrALAZINE HCl Tablets Recalled by The Harvard Drug Group Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification result...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 24, 2022· International Science & Technology, LP, DBA Diamatrix Ltd.

Recalled Item: Outer Packaging Label: Protekt Sharps Safety Knives - 44620MU Recalled by...

The Issue: Surgical knives may contain incorrect description printed on handles....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2022· Boston Scientific Corporation

Recalled Item: SpaceOAR Vue System Recalled by Boston Scientific Corporation Due to Users...

The Issue: Users need to be aware that embolism is a possible adverse event associated...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2022· ROi CPS LLC

Recalled Item: Regard Custom Procedure Kits containing BD Luer Lok Access Devices Recalled...

The Issue: Recalled devices were packaged in convenience kits.

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

Class III — Low RiskOngoing
Medical DeviceFebruary 24, 2022· Boston Scientific Corporation

Recalled Item: SpaceOAR System Recalled by Boston Scientific Corporation Due to Users need...

The Issue: Users need to be aware that embolism is a possible adverse event associated...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q.zen ceiling Recalled by Siemens Medical Solutions USA, Inc Due to If...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zeego Recalled by Siemens Medical Solutions USA, Inc Due to If the...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q zeego Recalled by Siemens Medical Solutions USA, Inc Due to If the...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q biplane Recalled by Siemens Medical Solutions USA, Inc Due to If the...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q.zen floor Recalled by Siemens Medical Solutions USA, Inc Due to If...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q.zen biplane Recalled by Siemens Medical Solutions USA, Inc Due to If...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee ceiling Recalled by Siemens Medical Solutions USA, Inc Due to If...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q floor Recalled by Siemens Medical Solutions USA, Inc Due to If the...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

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

Class II — Potential Health HazardOngoing