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. 1,942 recalls have been distributed to Florida in the last 12 months.
Showing 28081–28100 of 55,837 recalls
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: 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: 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: 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: 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: 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: 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: Foley Temperature Sensor Catheter 8FR Recalled by Degania Silicone, Ltd. Due...
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: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6)...
The Issue: The flow rate test verification was not properly executed for certain Sigma...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ossur Skull Pin Recalled by Ossur Americas Due to Halo system products...
The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ossur Recalled by Ossur Americas Due to Halo system products labeled MR...
The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott TECNIS 1-Piece Aspheric Acrylic IOL with the TECNIS iTEC Recalled by...
The Issue: Expired intraocular lenses were distributed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ossur CB Resolve Recalled by Ossur Americas Due to Halo system products...
The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ossur OB Resolve Recalled by Ossur Americas Due to Halo system products...
The Issue: Halo system products labeled MR conditional will undergo confirmatory safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.