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. 2,815 recalls have been distributed to Florida in the last 12 months.
Showing 16681–16700 of 30,686 recalls
Recalled Item: QUIKFLAP Recalled by Stryker Leibinger GmbH & Co. KG Due to After a three...
The Issue: After a three year term, there is a potential for the external packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXS PP Recalled by Stryker Leibinger GmbH & Co. KG Due to After a three year...
The Issue: After a three year term, there is a potential for the external packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUIKFLAP Recalled by Stryker Leibinger GmbH & Co. KG Due to After a three...
The Issue: After a three year term, there is a potential for the external packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXS PP Recalled by Stryker Leibinger GmbH & Co. KG Due to After a three year...
The Issue: After a three year term, there is a potential for the external packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clarity Urocheck 10SG Urinalysis Strips Recalled by Clarity Diagnostics Llc...
The Issue: Clarity Diagnostics LLC discovered specific lots of Clarity 10SG Strips are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aplicare Povidone Iodine Prep Pads packaged within Portex Pro-Vent Arterial...
The Issue: The povidone iodine prep pads packaged with the arterial blood sampling kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUIKFLAP Recalled by Stryker Leibinger GmbH & Co. KG Due to After a three...
The Issue: After a three year term, there is a potential for the external packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXS PP Recalled by Stryker Leibinger GmbH & Co. KG Due to After a three year...
The Issue: After a three year term, there is a potential for the external packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aplicare Povidone Iodine Prep Pads packaged within Portex Pulsator Arterial...
The Issue: The povidone iodine prep pads packaged with the arterial blood sampling kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Partial Knee System Spacer Block Alignment Tower Recalled by Zimmer...
The Issue: The PPK System Spacer Block Alignment Tower mating feature that mates with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature sensing catheter 16FR Recalled by Degania Silicone, Ltd. Due to...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foley Catheter with temperature sensor 400TM 16FR Recalled by Degania...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature sensor Foley catheter 10FR Recalled by Degania Silicone, Ltd....
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensor Catheter 16FR Recalled by Degania Silicone, Ltd. Due to...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature sensing catheter 18FR Recalled by Degania Silicone, Ltd. Due to...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foley Catheter with temperature sensor 400TM 8FR Recalled by Degania...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foley Temperature Sensor Catheter 12FR Recalled by Degania Silicone, Ltd....
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foley Temperature Sensor Catheter 14FR Recalled by Degania Silicone, Ltd....
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.