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. 2,923 recalls have been distributed to Florida in the last 12 months.
Showing 4001–4020 of 55,837 recalls
Recalled Item: AMT Mini Enteral Extension Set Recalled by Applied Medical Technology Inc...
The Issue: The extension sets subject to this recall have ENFit connections, although...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Unitek Transbond Plus Self-Etching Primer (100 unit Recalled by 3M Unitek...
The Issue: Due to an increase of complaints for bracket bond failures and skin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Crab Cheese Rangoon Recalled by SE Tampa Inc dba Tampa Food Due to...
The Issue: Undeclared allergens: Milk, Soy, Crustacea Shellfish, Fish
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Olanzapine Tablets Recalled by Macleods Pharmaceuticals Ltd Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AURYON LASER SYSTEM 100-120 VAC. Model Number: EXM001. Product Number:...
The Issue: Potential for procedural delays or interruptions during use of the Auryon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xhibit Telemetry Receiver Recalled by Spacelabs Healthcare, Inc. Due to...
The Issue: Telemetry receiver systems may experience a Windows proxy Issue causing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xhibit Telemetry Receiver with Software Recalled by Spacelabs Healthcare,...
The Issue: Telemetry receivers with affected software versions may experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eclipse PRO The Spacelabs model 98700 is a Recalled by Spacelabs Healthcare,...
The Issue: Due to a manufacturing error the incorrect device serial number was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eclipse Mini The Eclipse MINI Model 98900 is Recalled by Spacelabs...
The Issue: Due to a manufacturing error the incorrect device serial number was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.