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. 967 recalls have been distributed to Florida in the last 12 months.
Showing 46621–46640 of 55,837 recalls
Recalled Item: Columbia Agar with 5% Sheep Blood Columbia Agar with 5% Recalled by Becton...
The Issue: A low level of surface and subsurface contamination of Listeria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TrypticaseTM Soy Agar with 5% Sheep Blood (TSA IITM) // Recalled by Becton...
The Issue: A low level of surface and subsurface contamination of Listeria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Medical System Allura Xper X-Ray Angiographic Recalled by Philips...
The Issue: In certain circumstances, a software error can lead to a situation where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDC Anaerobe 5% Sheep Blood Agar CDC Anaerobe 5% Sheep Recalled by Becton...
The Issue: A low level of surface and subsurface contamination of Listeria...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heparin Sodium in 5% Dextrose Injection Recalled by Hospira Inc. Due to Lack...
The Issue: Lack of Assurance of Sterility: Confirmed consumer report of fluid leaking...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DENBLAN Anticavity Fluoride Toothpaste Recalled by Estee Lauder Inc Due to...
The Issue: Stability Data Does Not Support Expiry
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GreenSmoothieGirl TriOmega Superfood Recalled by Green Smoothie Girl Due to...
The Issue: The products contain Organic Sprouted Chia Powder that may be contaminated...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kirkland Signature Coarse Ground Malabar Pepper Recalled by Olde Thompson,...
The Issue: Olde Thompson is recalling Kirkland Signature Coarse Ground Malabar Black...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Adaptor Recalled by Teleflex Medical Due to The seals of the adaptor...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquapak 640 SW Recalled by Teleflex Medical Due to The seals of the adaptor...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquapak 340 SW Recalled by Teleflex Medical Due to The seals of the...
The Issue: The seals of the respiratory gas humidifier adaptor packaging may be creased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquapak 640 SW Recalled by Teleflex Medical Due to The seals of the adaptor...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Artis or Artis zee system Product Usage: Axiom Artis Recalled by...
The Issue: There is a potential problem with the AXIOM Artis or Artis zee system in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraStream Peel Away Kit Recalled by Argon Medical Devices, Inc Due to...
The Issue: UltraStream Chronic Hemodialysis Catheter may develop cracks on the red...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraStream Chronic Hemodialysis Catheter Standard Kit Recalled by Argon...
The Issue: UltraStream Chronic Hemodialysis Catheter may develop cracks on the red...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DMI Duro-Med Industries Rollator Transport Chair Recalled by Briggs Medical...
The Issue: There have been 5 customer reports of a 501-1018 series DMI Rollator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Excelsior Medical Sterile Triple Lead Tubing Set and Sterile Heavy Recalled...
The Issue: There is a potential for a leak. A molding defect in the connector that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraStream Exchange Kit Model Numbers 32001524 (24 cm) Recalled by Argon...
The Issue: UltraStream Chronic Hemodialysis Catheter may develop cracks on the red...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquapak 340 SW Recalled by Teleflex Medical Due to The seals of the adaptor...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquapak SW/EAU Recalled by Teleflex Medical Due to The seals of the adaptor...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.