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. 2,021 recalls have been distributed to Florida in the last 12 months.
Showing 20261–20280 of 55,837 recalls
Recalled Item: Multi Display Manager in the Artis Systems (Image-Intensified Fluoroscopic...
The Issue: Artis systems containing a Multi Display Manager of a specific lot, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dover 100% Silicone Foley Catheter with Temperature Sensor 14FR 5CC2W...
The Issue: Temperature sensing catheters failed to meet the established calibrated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dover 100% Silicone Foley Catheter with Temperature 16FR 5CC2W Recalled by...
The Issue: Temperature sensing catheters failed to meet the established calibrated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dover 100% Silicone Silver-Hydrogel Coated Foley Catheter with Temperature...
The Issue: Temperature sensing catheters failed to meet the established calibrated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dover 100% Silicone Silver-Hydrogel Coated Premium Urine Meter Foley Tray...
The Issue: Temperature sensing catheters failed to meet the established calibrated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Giraffe OmniBed with installed Servo Oxygen module. Infant incubator and...
The Issue: Potential for certain Giraffe Incubators and Giraffe OmniBeds to deliver a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Giraffe Incubator with installed Servo Oxygen module. Infant incubator....
The Issue: Potential for certain Giraffe Incubators and Giraffe OmniBeds to deliver a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Benefiber Prebiotic Fiber Supplement Recalled by Glaxosmithkline Consumer...
The Issue: Fiber prebiotic product potentially contaminated with small plastic pieces
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Benefiber Healthy Shape Prebiotic Fiber Supplement Recalled by...
The Issue: Fiber prebiotic product potentially contaminated with small plastic pieces
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DDU-2400EN Lifeline PRO Recalled by Defibtech, LLC Due to A component issue...
The Issue: A component issue may cause the AED to abort a shock delivery or reset...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DDU-2450 Lifeline ECG Model Numbers DDU-A2450EN DDU-E2450DE DDU-E2450EN...
The Issue: A component issue may cause the AED to abort a shock delivery or reset...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillators Model numbers M3535A Recalled...
The Issue: HeartStart XL MonitorlDefibrillators may not have been included in prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DDU-2300 Lifeline/ReviveR View Recalled by Defibtech, LLC Due to A component...
The Issue: A component issue may cause the AED to abort a shock delivery or reset...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1/2 - 3/8 REDUC CONN Recalled by LivaNova USA Inc. Due to The firm has...
The Issue: The firm has identified through internal tests that the sterile barrier of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extremities Recalled by Medtronic Sofamor Danek USA Inc Due to Product may...
The Issue: Product may not maintain its setting characteristics for the labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal Sterile Custom Kits packaged as a Piggy Back with Recalled by...
The Issue: DeRoyal manufactured procedure packs using BDPosiFlush syringes which were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Bone Void Filler Recalled by Medtronic Sofamor Danek USA Inc Due...
The Issue: Product may not maintain its setting characteristics for the labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Disposable Connectors ASY CONN REDUCER 1/2 X 3/8 24 Recalled by...
The Issue: The firm has identified through internal tests that the sterile barrier of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Disposable Connectors ASY 3/16 X 3/16 STR CONNW/LL24. REF/ Recalled...
The Issue: The firm has identified through internal tests that the sterile barrier of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Disposable Connectors ASY Y CONN 3/8 X 3/8 X Recalled by LivaNova...
The Issue: The firm has identified through internal tests that the sterile barrier of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.