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. 2,754 recalls have been distributed to Florida in the last 12 months.
Showing 19001–19020 of 30,686 recalls
Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...
The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kelyniam Custom Skull Implant (CSI) Recalled by Kelyniam Global, Inc. Due to...
The Issue: Significant design changes made to the Custom Skull Implant (CSI) devices,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nicolet¿ Elite¿ 3 MHz OB Probe Recalled by Natus Neurology Inc Due to Some...
The Issue: Some of the Elite 2 and 3 Obstetric probes and 5 MHz Vascular Probes may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sorin Group Aortic Arch Cannula Recalled by Sorin Group USA, Inc. Due to...
The Issue: Identification of excess plastic on the tip of the cannula.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nicolet¿ Elite¿ 2 MHz OB Probe Recalled by Natus Neurology Inc Due to Some...
The Issue: Some of the Elite 2 and 3 Obstetric probes and 5 MHz Vascular Probes may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penumbra 3D Revascularization Device It is indicated for used in Recalled by...
The Issue: Penumbra has identified an issue in these four lots involving a raw material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nicolet¿ Elite¿ 5 MHz Vascular Probe Recalled by Natus Neurology Inc Due to...
The Issue: Some of the Elite 2 and 3 Obstetric probes and 5 MHz Vascular Probes may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nicolet¿ Elite¿ 2 MHz OB Water Proof Probe Recalled by Natus Neurology Inc...
The Issue: Some of the Elite 2 and 3 Obstetric probes and 5 MHz Vascular Probes may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu-Chek Connect diabetes management software app Recalled by Roche...
The Issue: Certain iOS and Android App versions contain a program error (bug) in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu-Chek Connect Diabetes Management App Recalled by Roche Diabetes Care,...
The Issue: Certain iOS and Android App versions contain a program error (bug) in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAKO RIO Standard System Recalled by Mako Surgical Corporation Due to An...
The Issue: An intermittent electrical problem that could lead to a loss of system power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath A-Kit Recalled by...
The Issue: An incomplete seal at the chevron end of the primary packaging of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThermaSure(TM) Recalled by Cenorin, LLC Due to Dryer unit not heating....
The Issue: Dryer unit not heating. Manufacturing issue causes the terminal block to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...
The Issue: An incomplete seal at the chevron end of the primary packaging of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath A-Kit Recalled by...
The Issue: An incomplete seal at the chevron end of the primary packaging of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...
The Issue: An incomplete seal at the chevron end of the primary packaging of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...
The Issue: An incomplete seal at the chevron end of the primary packaging of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...
The Issue: An incomplete seal at the chevron end of the primary packaging of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal(R) Dolphin Inflation Device Recalled by DeRoyal Industries Inc Due...
The Issue: Lack of sterility assurance. There is a defect in the primary packaging of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...
The Issue: An incomplete seal at the chevron end of the primary packaging of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.