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 25801–25820 of 30,686 recalls
Recalled Item: PERSONA (TM) The Personalized Knee System Tibial General Instrument Tray...
The Issue: The firm discovered that the current Personal Tibial/General Fixed Bracket...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panthera-Puncher 9 . Panthera-Puncher 9 is a sample transfer instrument...
The Issue: Risk of incorrect results from samples prepared with Panthera-Puncher 9
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERSONA (TM) The Personalized Knee System Tibial General Instrument Tray...
The Issue: The firm discovered that the current Personal Tibial/General Fixed Bracket...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood pressure (BP) circuit of the ANSAR ANX-3.0 Autonomic Monitor Recalled...
The Issue: The blood pressure (BP) circuit occasionally fails to inflate the blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IP5 Information Portal The Expression Information Portal (Model IP5)...
The Issue: The wireless function of the IP5 radio could be interrupted causing loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Recalled by Teleflex Medical Due to There is a possibility the handle...
The Issue: There is a possibility the handle of the laryngoscope may heat up and melt...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens syngo Imaging XS Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Siemens has become aware of the potential malfunction when using syngo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reliance 1227 Cart and Utensil Washer/Disinfector Product Usage: Usage: The...
The Issue: STERIS has identified that deformation of the washers door handle pin may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHAROS Excimer Laser Recalled by Ra Medical Systems Inc Due to RA Medical...
The Issue: RA Medical Systems is recalling the PHAROS EX-308 Excimer Laser because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PerkinElmer Specimen Gate Screening Center software Recalled by PerkinElmer...
The Issue: Potential for demographic information and test result to be mismatch.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The STERIS 4085 General Surgical Table Product Usage: is an Recalled by...
The Issue: STERIS engineering analysis has determined the D1 pressure switch in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Patient Data Manager 2.0 (Content manager 2.0 Recalled by Brainlab AG Due to...
The Issue: The following defects have been identified for data loaded with Patient Data...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Life Force Chamber Product Usage:The product is intended for restful...
The Issue: The Life Force chamber is marketed and promoted as a medical device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affinity¿ Four Birthing Bed Recalled by Hill-Rom, Inc. Due to The attachment...
The Issue: The attachment latch mechanism can become bent depending on user handling....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solanas 2.1mm FIXED DEPTH DRILL Recalled by Alphatec Spine, Inc. Due to...
The Issue: Alphatec Spine is recalling the 2.1mm Fixed Depth Drill 10mm because they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Esaote PA230E Transducer A portable and cart base ultrasound system Recalled...
The Issue: Using the PA230E transducer with a user-defined setting with the output...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxygen Mask Recalled by Salter Labs Due to The case label correctly states...
The Issue: The case label correctly states partial rebreather but the insert label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The synthetic non-absorbable surgical sutures CARDIOFLON Evolution are...
The Issue: A potential splitting of the surface treatment of the thread ends on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Cardiology Hemo. McKesson Cardiology" Hemo is intended for complete...
The Issue: McKesson Cardiology Hemo front-end parameter boxes must undergo annual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Essential NEO Recalled by Karl Storz Endoscopy Due to KARL STORZ...
The Issue: KARL STORZ Endoscopy-America is recalling the Essential NEO because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.