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 12001–12020 of 55,837 recalls
Recalled Item: Tuscan Garden Restaurant Style Italian Dressing Recalled by Treehouse Foods...
The Issue: Undeclared soy and wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Hamilton-C6 Recalled by Hamilton Medical AG Due to Due to a malfunction...
The Issue: Due to a malfunction related to the backlight on the ventilator screen. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AutoPulse Li-ion Battery used on the AutoPulse Resuscitation System Model...
The Issue: Due to increase in Li-Ion Battery failures
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ampicillin for Injection Recalled by Viatris Inc Due to Presence of...
The Issue: Presence of Particulate Matter: A complaint was received for the presence of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rifampin Capsules Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed impurities/degradation specifications: Finished product exceeds the 5...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rifampin Capsules Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed impurities/degradation specifications: Finished product exceeds the 5...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: WEB Detachment Controller Recalled by MICROVENTION INC. Due to Detachment...
The Issue: Detachment controller, of an aneurysm embolization system, has an out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GORE CARDIOFORM ASD Occluder. cardiovascular implant. Recalled by W L Gore &...
The Issue: Due to manufacturing records (Release Test Results) indicating "Failed".
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: oxyTOCIN 30 Units/500 mL (0.06 Units/mL) added to 0.9% Sodium Chloride...
The Issue: Incorrect Product Formulation: Oxytocin 30 units was added to an IV bag of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Insulin Pump/Model: MiniMed 620G/ MMT-1750 MiniMed 640G/ MMT-1711 Recalled...
The Issue: Medtronic identified a cybersecurity vulnerability in the MiniMed 600 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Teleflex Medical RUSCH Pocket Pac i.c. Closed System Intermittent Catheter...
The Issue: Product may not be sterile
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Insulin Pump/Model: MiniMed 630G/ MMT-1715 Recalled by Medtronic MiniMed Due...
The Issue: Medtronic identified a cybersecurity vulnerability in the MiniMed 600 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci X (IS4200) and Xi (IS4000) systems Recalled by Intuitive Surgical,...
The Issue: Inadvertent energy delivery from surgical system instrument if 1) Force...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex MP Port Titanium Low Profile Implanted Port with 5F Recalled by...
The Issue: Printed Instructions for Use (IFU) not shipped with device. The Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS pheno Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...
The Issue: Siemens has become aware of three potential software issues with ARTIS pheno...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clonidine Hydrochloride Tablets Recalled by UNICHEM PHARMACEUTICALS USA INC...
The Issue: Product mix-up:0.2 mg strength Clonidine Hydrochloride Tablets, USP in a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Indian Gooseberry Alcohol-Free Extract Recalled by Secrets Of The Tribe Due...
The Issue: Product has elevated level of lead.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Amla Alcohol-Free Extract Recalled by Secrets Of The Tribe Due to Product...
The Issue: Product has elevated level of lead.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dutch Red Potatoes with Dijon Mustard Sauce. NET WT. 1 Recalled by World...
The Issue: Dutch Red Potatoes were packed with a Dijon Mustard Sauce packet that did...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 125 series iGO2 Portable Oxygen Concentrator-indicated for the...
The Issue: An unapproved adhesive used to manufacture the accumulator tank sub assembly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.