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. 2,622 recalls have been distributed to Florida in the last 12 months.
Showing 44161–44180 of 55,837 recalls
Recalled Item: AQUAPAK 640 SW Recalled by Teleflex Medical Due to Foreign Object Contamination
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI¿ Humidifier Adaptor Recalled by Teleflex Medical Due to Foreign...
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUAPAK 640 SW Recalled by Teleflex Medical Due to Foreign Object Contamination
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUAPAK SW/EAU STERILE Recalled by Teleflex Medical Due to Foreign Object...
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUAPAK 640 SW Recalled by Teleflex Medical Due to Foreign Object Contamination
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUAPAK 340 SW Recalled by Teleflex Medical Due to Foreign Object Contamination
The Issue: The packages may contain foreign material (black particles).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Honey & Oat Mixers ready-to-eat dry cereal sold under the Recalled by...
The Issue: Undeclared almonds
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sony LMD-1951MD Recalled by Sony Medical Systems Due to Tthe medical monitor...
The Issue: Tthe medical monitor has either not turned on or has lost image during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LMA (Laryngeal Mask Airway) Supreme (New Cuff) Size 5 Recalled by Teleflex...
The Issue: The labelling of units from the affected lot indicates that it contains a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KYPHON EXPRESS Recalled by Medtronic Sofamor Danek USA Inc Due to The...
The Issue: The product, labeled as containing, one bevel-tipped instrument and one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartSite Low Sorbing Infusion Set Recalled by CareFusion 303, Inc. Due to...
The Issue: CareFusion is recalling the SmartSite Low Sorbing Infusion set due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.plaza: Syngo.plaza is a Picture Archiving and Communication System...
The Issue: In case of a system crash, images may not be written to the hard disk and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Recalled by Noven...
The Issue: Defective Delivery System: One lot exceeded the mechanical peel specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: My Spice Sage CUMIN GROUND under the following labels and Recalled by...
The Issue: Cumin may contain undeclared peanut protein.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Melatonin Control- Released Tablets Recalled by HVL, LLC Due to Bottles...
The Issue: Bottles contained a vegetarian digestive enzyme dietary supplement instead...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Servo-I ventilator system CO2 analyzer. Part number 65 23 588. Recalled by...
The Issue: A calibration problem was detected in a specific number of the Servo-I...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAQUET Recalled by Teleflex Medical Due to Defects: Cracks that may occur in...
The Issue: Defects: Cracks that may occur in the center of the corrugated flex tube of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 980 Ventilator System Recalled by Covidien LP (formerly...
The Issue: Covidien is issuing a voluntary field action for all Puritan Bennett 980...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.