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. 1,819 recalls have been distributed to Florida in the last 12 months.
Showing 45521–45540 of 55,837 recalls
Recalled Item: MINI PEDIATRIC Radiotransparent Electrode Recalled by ConMed Corporation Due...
The Issue: Philips Healthcare made changes to the design of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CONMED PEDIATRIC R2 Multifunction Electrodes Recalled by ConMed Corporation...
The Issue: Philips Healthcare made changes to the design of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS CHEMISTRY PRODUCTS TRIG Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: Potential for biased results using the specific lot of VITROS CHEMISTRY...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Small Electric Drive (SED) Recalled by Synthes (USA) Products LLC...
The Issue: The device may operate solely in reverse mode, not operate in reverse mode...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Healon EndoCoat Ophthalmic Viscosurgical Device 3% sodium hyaluronate...
The Issue: AMO has received complaints where the finger grip dislodged while depressing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADULT Radiotransparent Electrode Recalled by ConMed Corporation Due to...
The Issue: Philips Healthcare made changes to the design of the connection between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiac Function Analysis Software Product Data No. MPDCT0301EAD CSCF-003A...
The Issue: Potential problem with the cardiac function analysis software (CFA)....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiac Function Analysis Software Product Data No. MPDCT0301EAD CSCF-003A...
The Issue: Potential problem with the cardiac function analysis software (CFA)....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Q-Station Quantification Software. Q-Station 3.0 with a2DQ and/or aCMQ...
The Issue: When using the QLAB Auto 2D Quantification (a2DQ) and Auto Cardiac Motion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polyflux Revaclear Max Dialyzer Recalled by Gambro Renal Products Inc Due to...
The Issue: Gambro is initiating a field action for Polyflux Revaclear Dialyzer and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIQ 7 Ultrasound System Recalled by Philips Ultrasound, Inc. Due to When...
The Issue: When using the QLAB Auto 2D Quantification (a2DQ) and Auto Cardiac Motion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Additional devices identified in new FSN MA-FCO 83000190: QLAB versions...
The Issue: When using the QLAB Auto 2D Quantification (a2DQ) and Auto Cardiac Motion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polyflux Revaclear Dialyzer Recalled by Gambro Renal Products Inc Due to...
The Issue: Gambro is initiating a field action for Polyflux Revaclear Dialyzer and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIQ 5 Ultrasound System Recalled by Philips Ultrasound, Inc. Due to When...
The Issue: When using the QLAB Auto 2D Quantification (a2DQ) and Auto Cardiac Motion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-sterile drape Recalled by Novadaq Technologies, Inc. Due to Mislabeling
The Issue: Non sterile-drape LUNA drape was inadvertently mislabeled with an additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch & Lomb Stellaris PC w/ Laser Recalled by Bausch & Lomb Inc Due to A...
The Issue: A software anomaly was identified where the system may automatically...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUNA Chest Recalled by Novadaq Technologies, Inc. Due to Mislabeling
The Issue: Non sterile-drape LUNA drape was inadvertently mislabeled with an additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch & Lomb Stellaris PC w/ Laser Upgrade BL1433 (Stellaris Recalled by...
The Issue: A software anomaly was identified where the system may automatically...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch & Lomb Stellaris PC w/ Laser Upgrade BL14334 (Stellaris Recalled by...
The Issue: A software anomaly was identified where the system may automatically...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView product code: 882478 BrightView X product code: 882480 BrightView...
The Issue: Software issues
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.