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.
Showing 30021–30040 of 30,686 recalls
Recalled Item: IDEV Technologies SUPERA VERITAS Interwoven Self-Expanding Nitinol Stent...
The Issue: There was an error on the outer labeling of this device. The inner label was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Isothermal Breathing Circuit Accessory - Infant Patient Y Connector...
The Issue: The Y adapter within the breathing circuit may spontaneously crack, causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trinity Biotech Recalled by Clark Laboratories, Inc. (dba,Trinity Biotech...
The Issue: The Positive Control for the Captia Varicella-Zoster Virus (VZV) IgG Kit has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Isothermal Breathing Circuit Recalled by Carefusion 2200 Inc Due to...
The Issue: The Y adapter within the breathing circuit may spontaneously crack, causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Isothermal Breathing Circuit Recalled by Carefusion 2200 Inc Due to...
The Issue: The Y adapter within the breathing circuit may spontaneously crack, causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microbiologics 217 Osseo Avenue North Recalled by Microbiologics Inc Due to...
The Issue: Microbiologics is recalling a number of lots of KWIK-QC Gram Stain Slides....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: This voluntary medical device correction is related to Alcon products...
The Issue: This medical device correction is related to Alcon products that present a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC unit model 8015 Product Usage: The device is Recalled by...
The Issue: The recall was initiated because the Alaris PC unit model 8015 has a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Volume Viewer Plus 5.x (Advantage Workstation 4.2) Volume...
The Issue: Incorrect views and measurements possible. GE Healthcare became aware of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AdvantageSim MD versions 7.4 through 7.6 Recalled by GE Healthcare, LLC Due...
The Issue: It was reported by a customer site that when using GE AdvantageSim MD on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of inaccurate Scale factor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Advantage CT/PET Fusion for Advantage Windows Workstation with Volume...
The Issue: GE Healthcare has become aware of a potential safety issue due to incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Advantage Workstations Recalled by GE Healthcare, LLC Due to...
The Issue: GE Healthcare is informing you of incorrect measurements when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Seno Advantage 1.x Recalled by GE Healthcare, LLC Due to GE Healthcare...
The Issue: GE Healthcare has become aware of an issue associated with the magnification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra(TM) Jarit(R) Take-Apart Endoscopic Instruments. Integra(TM) Jarit(R)...
The Issue: The Integra(TM) Jarit(R) Take-Apart Laparoscopic Instrument shafts were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LMA Esophageal Intubation Detector (EID) Recalled by LMA North America Inc...
The Issue: The recall was initiated because LMANA has received a complaint that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliSpace Portal software and Extended Brillance Workspace software...
The Issue: The Intellispace Portal software and Extended Brillance Workspace software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bipolar Forceps model number: S02-XXX Recalled by Stingray Surgical...
The Issue: On 05/23/2012, Stingray Surgical Products, LLC., Boca Raton, FL initiated a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intellispace Portal software. Intellispace Portal is a multimodality thin...
The Issue: Philips is issuing a software update to the Intellispace Portal systems to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Triage BNP PN 98000XR Intended to be used as Recalled by Alere San...
The Issue: Certain lots of the affected products may have significantly decreased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.