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 28421–28440 of 30,686 recalls
Recalled Item: BrightView SPECT gamma camera for Emission Computed Tomography Recalled by...
The Issue: Philips has received one report from the field that there was an unexpected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mini Cannulated Titanium Headed and Headless Screw Set and 2.5 Recalled by...
The Issue: Faded and wrong markings on bone screw Countersink/Depth Gauge instruments...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: embla Embletta Gold (It functions as a Polysomnography Recorder and Recalled...
The Issue: Calibration error for Embla Embletta Gold units calibrated through service...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEXSTENT Femoropopliteal Self-Expanding Stent System. Product Usage: The...
The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEXSTENT Biliary Self-Expanding Stent System. Product Usage: The FSS...
The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEXSTENT Femoropopliteal Self-Expanding Stent System. Product Usage: The...
The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEXSTENT Biliary Self-Expanding Stent System. Product Usage: The FSS...
The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEXSTENT Femoropopliteal Self-Expanding Stent System. Product Usage: The...
The Issue: Holes and/or tears can be introduced in the FLEXSTENT¿ inner pouch under...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fisher & Paykel Healthcare ICON CPAP (continuous positive airway pressure)....
The Issue: Fisher and Paykel Healthcare is recalling the ICON CPAP units because there...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HB1C Flex(R) Reagent Cartridge (DF105A Recalled by Siemens Healthcare...
The Issue: Positive bias on the lots listed compared to alternate methods and a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) Adult Manual Resuscitator Recalled by Carefusion 2200 Inc Due to...
The Issue: CareFusion has received four (4) customer reports of a component (oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HbA1c Flex(R) reagent cartridge (K3105A Recalled by Siemens Healthcare...
The Issue: Positive bias on the lots listed compared to alternate methods and a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD CYCLESURE 24 Biological Indicator (BI) The STERRAD CYCLESURE 24...
The Issue: Advanced Sterilization Products is recalling certain lots of STERRAD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Case Lid and Base (Inspan Recalled by SpineFrontier, Inc. Due to Non-toxic...
The Issue: Non-toxic inks, used on the silk screen graphics of the case bases and lids,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brainlab Cranial Navigation System: An Image Guided Surgery System /...
The Issue: Software Error: The effect of setup on overall navigation accuracy could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Enterprise Archive is a software product for receiving Recalled...
The Issue: GE Healthcare has become aware of a potential data loss issue associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 90 Degree Cannulated Infant Blade Plate 25mm x 5mm x Recalled by...
The Issue: Post Market Surveillance of the 90 degree Cannulated Infant Blade Plate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 90 Degree Cannulated Infant Blade Plate 35mm x 5mm x Recalled by...
The Issue: Post Market Surveillance of the 90 degree Cannulated Infant Blade Plate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 90 Degree Cannulated Infant Blade Plate 30mm x 5mm x Recalled by...
The Issue: Post Market Surveillance of the 90 degree Cannulated Infant Blade Plate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zilver PTX Drug-Eluting Peripheral Stent Recalled by Cook, Inc. Due to Cook...
The Issue: Cook Medical has received a small number of complaints related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.