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. 2,706 recalls have been distributed to Florida in the last 12 months.
Showing 32401–32420 of 55,837 recalls
Recalled Item: Ventolin HFA (albuterol sulfate) Inhalation Recalled by GlaxoSmithKline, LLC...
The Issue: Defective Delivery System: Elevated number of units with out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Beckman Coulter Synchron AQUA CAL Level 1 Recalled by Beckman Coulter Inc...
The Issue: The firm identified a negative shift of 5mmol/L for sodium recovery in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD¿ High Volume Administration Set with FlowStop Recalled by Smiths...
The Issue: One lot of CADD¿ High Volume Administration sets, part number 21-7381-24,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multiphor II Electrophoresis System GE HealthCare Product Number: 18-1018-06...
The Issue: Potential for electric shock in the case of a failure to install the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MesaLabs Conductivity Standard Solution Recalled by Mesa Laboratories, Inc....
The Issue: Mesa Laboratories is recalling Conductivity/TDS Calibrator Solution due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nutri-Dyn Calcium D-Glucarate Plus Recalled by Nutri-Dyn Midwest, Inc. Due...
The Issue: During production of St. John's Wort, Lot 160876, a number of bottles were...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Tubing Pack Convenience Kit Recalled by Terumo Cardiovascular Systems Corp...
The Issue: Kit was labeled with the incorrect Expiration Date of April 30, 2019.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Queso Fresco x LB (Barra)/ Whole Milk Cheese Recalled by Global Garlic, Inc....
The Issue: Product contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sara Lee CP Quiche 10 Spinach Recalled by Tyson Foods, inc. Due to Potential...
The Issue: The firm is voluntarily recalling multiple lots of frozen Chef Pierre 10...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chef Pierre 10 Spinach Quiche Recalled by Tyson Foods, inc. Due to Potential...
The Issue: The firm is voluntarily recalling multiple lots of frozen Chef Pierre 10...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: De Mi Pais Recalled by Global Garlic, Inc. Due to Potential Listeria...
The Issue: Product contaminated with Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kite Hill Mushroom and Ricotta Ravioli Recalled by Lyrical Foods Inc Due to...
The Issue: Ingredient statement for Lyrical Foods Mushroom and Ricotta Flavor Ravioli...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Clear Flashback Needle 7cm x 18G AMC/4 Recalled by Argon Medical Devices,...
The Issue: Argon Medical has received a complaint from one of their distributors of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix PMIC-107 Recalled by Becton Dickinson & Co. Due to BD has...
The Issue: BD has recently confirmed quality control failures, related to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima MR450w 1.5T Product Usage: The Optima MR450w 1.5T system Recalled by...
The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips DigitalDiagnost 3.1.x X-Ray System Recalled by Philips Electronics...
The Issue: During recent evaluations of the Philips DigitalDiagnost 3.1.x, we have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5T Signa HDxt Recalled by GE Medical Systems, LLC Due to Possible...
The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima MR750 3.0T Product Usage: The Optima MR450 1.5T system Recalled by GE...
The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brivo MR355 Recalled by GE Medical Systems, LLC Due to Possible incorrect...
The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Signa PET/MR (K163619 Recalled by GE Medical Systems, LLC Due to Possible...
The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.