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. 2,824 recalls have been distributed to Florida in the last 12 months.
Showing 15561–15580 of 30,686 recalls
Recalled Item: Tritanium Posterior Lumbar (PL) cage intervertebral body fusion implant....
The Issue: The surgical technique is being updated to caution against misuse due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RESERVOIR "Y" ADAPTER Recalled by Medtronic Perfusion Systems Due to...
The Issue: Medtronic discovered that certain Y-connectors included in the suction lines...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SUCTION / ANTICOAGULATION ASSEMBLY (a) BTC93 (b) BTC98 Suction and Recalled...
The Issue: Medtronic discovered that certain Y-connectors included in the suction lines...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoform Dermal Template 2x2 Recalled by AROA BIOSURGERY Due to Potential...
The Issue: Potential for pouch seal failure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoform Dermal Template 2x2 Recalled by AROA BIOSURGERY Due to Potential...
The Issue: Potential for pouch seal failure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoform Dermal Template 4x5 Recalled by AROA BIOSURGERY Due to Potential...
The Issue: Potential for pouch seal failure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProtectIV¿ Plus Safety IV Catheter Recalled by Smiths Medical ASD Inc. Due...
The Issue: Certain lots of the Model 306701 ProtectIV¿ Plus Safety IV Catheter may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Recalled by Philips North America LLC Due to Affected...
The Issue: Affected lithium-ion batteries may contain a defective component (Thermal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Xi Surgical System Recalled by Intuitive Surgical, Inc. Due to Due...
The Issue: Due to a manufacturing variation in the arm that can result in a persistent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci X Surgical System Recalled by Intuitive Surgical, Inc. Due to Due...
The Issue: Due to a manufacturing variation in the arm that can result in a persistent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity i Ferritin Reagent Kit Recalled by Abbott Ireland Diagnostics...
The Issue: Abbott has become aware of a manufacturing issue that can result in damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity i TSH Reagent Kit Recalled by Abbott Ireland Diagnostics Division...
The Issue: Abbott has become aware of a manufacturing issue that can result in damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity i Progesterone Reagent Kit Recalled by Abbott Ireland Diagnostics...
The Issue: Abbott has become aware of a manufacturing issue that can result in damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity i Total Beta-hCG Reagent Kit Recalled by Abbott Ireland Diagnostics...
The Issue: Abbott has become aware of a manufacturing issue that can result in damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity i Estradiol Reagent Kit Recalled by Abbott Ireland Diagnostics...
The Issue: Abbott has become aware of a manufacturing issue that can result in damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity i Free T4 Reagent Kit Recalled by Abbott Ireland Diagnostics...
The Issue: Abbott has become aware of a manufacturing issue that can result in damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity i 25-OH Vitamin D Reagent Kit Recalled by Abbott Ireland Diagnostics...
The Issue: Abbott has become aware of a manufacturing issue that can result in damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power-LOAD Cot Fastening System Recalled by Stryker Medical Division of...
The Issue: The power load floor plates which hold the ambulance cot anchors in place...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: St. Jude Medical Confirm Rx Insertable Cardiac Monitor Recalled by Abbott...
The Issue: The device is unable to pair with the mobile app due to the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrex Suture Anchor Recalled by Arthrex, Inc. Due to Potentially lead to...
The Issue: Potentially lead to anchor breakage during insertion,
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.