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. 2,873 recalls have been distributed to Florida in the last 12 months.
Showing 11621–11640 of 55,837 recalls
Recalled Item: R&D CBC-3D Hematology Control: (1) CBC-3D Normal Pack Hematology Control...
The Issue: For one lot of CBC-3D Hematology Control, the Normal Level may exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis Angiographic Catheter Extensions. Used to transport fluid from the...
The Issue: There is a potential for separation at the male connector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow-c Anesthesia System (Product Code 6887700) Flow-e Anesthesia System...
The Issue: The power backup battery, under certain conditions, may exhibit reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adam's Polishes ALCOHOL BASED HAND SANITIZER Recalled by Adam's Polishes LLC...
The Issue: CGMP Deviations: Other lots of hand sanitizer are being recalled because...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Adam's Polishes ALCOHOL BASED HAND SANITIZER Recalled by Adam's Polishes LLC...
The Issue: Chemical Contamination: FDA analysis found 1 lot of Adam's Polishes ALCOHOL...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The Tomato Head Beet Hummus packaged in 8oz PPE plastic cups - 8 cups per...
The Issue: Potential Metal Fragments within product
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The Tomato Head Black Bean Sriracha Hummus packaged in 8oz Recalled by...
The Issue: Potential Metal Fragments within product
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medical Action INDUSTRIES INC. Port a Cath Kit Recalled by Medical Action...
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests Japan...
The Issue: Potential for falsely elevated specific IgE mold allergen reactivity with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests (600T)-...
The Issue: Potential for falsely elevated specific IgE mold allergen reactivity with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests OUS...
The Issue: Potential for falsely elevated specific IgE mold allergen reactivity with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HF Resection Electrodes Recalled by Olympus Corporation of the Americas Due...
The Issue: An incompatible HF cable may be packaged with the HF Resection Electrodes....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nestle Toll House Edible Chocolate Chip Cookie Dough packaged in Recalled by...
The Issue: Potential of foreign material within product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VADER Pedicle System Torque Wrench Recalled by Icotec Ag Due to During...
The Issue: During internal testing (at manufacturer site) of two torque wrench devices,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Moxifloxacin Ophthalmic Solution Recalled by Direct Rx Due to cGMP...
The Issue: cGMP deviation: discontinue of stability support for product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SynCardia Total Artificial Heart System (70CC): 500101-001 SynCardia Total...
The Issue: Due to tears reported tears in the cannula due to wear and tear stress.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HENRY SCHEIN Recalled by Stradis Medical, LLC dba Stradis Healthcare Due to...
The Issue: Medical and surgical procedure trays and kits underwent certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STRADIS HEALTHCARE Recalled by Stradis Medical, LLC dba Stradis Healthcare...
The Issue: Medical and surgical procedure trays and kits underwent certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STRADIS HEALTHCARE Recalled by Stradis Medical, LLC dba Stradis Healthcare...
The Issue: Medical and surgical procedure trays and kits underwent certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HENRY SCHEIN Recalled by Stradis Medical, LLC dba Stradis Healthcare Due to...
The Issue: Medical and surgical procedure trays and kits underwent certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.