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. 2,801 recalls have been distributed to Florida in the last 12 months.
Showing 17741–17760 of 30,686 recalls
Recalled Item: Artis one fluoroscopic x-ray system and patient table Artis one Recalled by...
The Issue: Certain patient table systems may have a missing or incorrectly installed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINC Benchtop Incubator (Mini Incubator) catalog (K-MINC-1000) G20079 is a...
The Issue: The temperature of the incubation lids of the MINC Bench top Incubators may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE HEALTHCARE CARESCAPE Central Station (CSCS) software version 2.0.2 The...
The Issue: CARESCAPE Central Station (CSCS) software version 2.0.2 units may experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ellex I.Science iTRACK 250A Recalled by Ellex iScience, Inc. Due to...
The Issue: Sterility failure found in one of the units in the lot.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PDS Plus Antibacterial (Polydioxanone) Suture Size 0 PDS Plus Violet...
The Issue: Three (3) lots were distributed with the incorrect expiry date on the label....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PDS Plus Antibacterial (Polydioxanone) Suture Size 0 PDS Plus Violet...
The Issue: Three (3) lots were distributed with the incorrect expiry date on the label....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PDS Plus Antibacterial (Polydioxanone) Suture Size 1 PDS PLUS Violet...
The Issue: Three (3) lots were distributed with the incorrect expiry date on the label....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RP RIVERPOINT MEDICAL 18G Brachy Grid B&K(TM) style Recalled by Riverpoint...
The Issue: Product is labeled with "CE", but is not yet approved in the European Union.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemodynamic monitoring system (HMS) Recalled by ICU Medical, Inc. Due to...
The Issue: When continuous cardiac output monitoring with a pulmonary artery catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diamedix Is-EBV-EA-D IgG Enzyme Immunoassay Test Kit for In Vitro Recalled...
The Issue: Contains a gel-like contaminant that may affect product performance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diamedix Is-Mumps IgG Enzyme Immunoassay Test Kit for In Vitro Recalled by...
The Issue: Contains a gel-like contaminant that may affect product performance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Artis angiographic x-ray system Recalled by Siemens Medical Solutions...
The Issue: Certain systems may have leaking of the plastic coolant couplings, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper systems with Certeray X-ray Generator located in regions...
The Issue: There is an increase in the failure rate of certain Anode Drive Units (ADU5)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioMerieux mini VIDAS System in combination with Quality Control VIDAS*...
The Issue: Increase of events affecting performance regarding pump clogging and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioMerieux VIDAS System in combination with Quality Control VIDAS* (QCV*)...
The Issue: Increase of events affecting performance regarding pump clogging and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diagnostic Ultrasound System Recalled by Toshiba American Medical Systems...
The Issue: The power supply unit may be damaged and may fail to start up when the power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percuvance(R) Percutaneous Shaft 36cm Recalled by Teleflex Medical Due to...
The Issue: There is potential for a piece of the distal tip on the Percuvance shaft to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percuvance(R) Percutaneous Shaft 29cm Recalled by Teleflex Medical Due to...
The Issue: There is potential for a piece of the distal tip on the Percuvance shaft to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MyLab Ultrasound System Recalled by ESAOTE S.P.A. Due to The ultrasound...
The Issue: The ultrasound system used in certain settings may result in overheating of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MyLab Ultrasound System Recalled by ESAOTE S.P.A. Due to The ultrasound...
The Issue: The ultrasound system used in certain settings may result in overheating of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.