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. 2,689 recalls have been distributed to Florida in the last 12 months.
Showing 34161–34180 of 55,837 recalls
Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The single use devices are provided sterile and do not have an expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The single use devices are provided sterile and do not have an expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The single use devices are provided sterile and do not have an expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The single use devices are provided sterile and do not have an expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Q Care Continue Care Kit for the non-ventilated patient Recalled by Sage...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: The expiration date of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Transderm Scop (scopolamine) Transdermal System Recalled by Sandoz Inc Due...
The Issue: Labeling: Incorrect Instructions:outer carton contains the incorrect...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mimvey Lo (estradiol and norethindrone acetate tablets USP) Recalled by Teva...
The Issue: Failed Impurities/Degradation Specifications: out of specification test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Check-Flo Hemostasis Assembly Recalled by Cook Inc. Due to Devices using a...
The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Micropuncture Check-Flo Performer Introducer Set Recalled by Cook Inc. Due...
The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Final Fit Software Version 1.11 and 1.12 Recalled by Nidek Inc Due to During...
The Issue: During treatment planning, the procedure was programmed with an unintended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Check-Flo Introducer Hausdorf-Lock Atrial Recalled by Cook Inc. Due to...
The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexor Radial Access Set Recalled by Cook Inc. Due to Devices using a...
The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Check-Flo Performer Introducer Set Recalled by Cook Inc. Due to Devices...
The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Angio WorkStation (XIDF-AWS801) used in conjunction with your Infinix System...
The Issue: It was found that during a procedure the Peak Skin Dose (PSD) value...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Check-Flo Performer Introducer Recalled by Cook Inc. Due to Devices using a...
The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TriForce Peripheral Crossing Set Recalled by Cook Inc. Due to Devices using...
The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 882478: BrightView X designed for single or dual detector nuclear Recalled...
The Issue: Four issues: 1. Motion controller problem stops scan and no data image...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 882482: BrightView XCT 882454 BrightView X upgrade to XCT Recalled by...
The Issue: Four issues: 1. Motion controller problem stops scan and no data image...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 882480: BrightView designed for single or dual detector nuclear imaging...
The Issue: Four issues: 1. Motion controller problem stops scan and no data image...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SHBG IMMULITE 2000/IMMULITE 2000 XPi For the in vitro diagnostic Recalled by...
The Issue: Certain lots of Sex Hormone Binding Globulin (SHBG) do not meet the thirty...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.