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. 2,710 recalls have been distributed to Florida in the last 12 months.
Showing 29061–29080 of 55,837 recalls
Recalled Item: Praluent 75 mg Pen (2 pens/Pkg) NDC 00024-5901-02 28 days supply Recalled by...
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Revlimid 5 mg oral cap NDC 59572-0405-28 28 days supply Recalled by Kroger...
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Capecitabine 150 mg Tablet NDC 00378-2511-91 28 days supply Recalled by...
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Letrozole 2.5 mg tab NDC 51991-0759-33 30 days supply Recalled by Kroger...
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Xalkori 250 mg cap NDC 00069-8140-20 30 days supply Recalled by Kroger...
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tecfidera 240 mg capsule NDC 64406-0006-02 30 days supply Recalled by Kroger...
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Temozolomide 20 mg NDC 43975-0253-05 28 days supply Recalled by Kroger...
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pediasure Liq. Vanilla G+G (CAN) #24 24 days supply Recalled by Kroger...
The Issue: Lack of Processing Controls.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Baxter Sigma Spectrum Infusion Pump with Master Drug Library (Version...
The Issue: Service technician improperly documented final release testing on product,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Sigma Spectrum Infusion Pump with Master Drug Library (Version...
The Issue: Service technician improperly documented final release testing on product,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Sigma Spectrum Infusion Pump with master Drug Library (Version...
The Issue: Service technician improperly documented final release testing on product,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Sigma Spectrum Infusion Pump with master Drug Library (Version...
The Issue: Service technician improperly documented final release testing on product,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Sigma Spectrum Infusion Pump with Master Drug Library (Version...
The Issue: Service technician improperly documented final release testing on product,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthopedic Salvage System (OSS) Modular Arthrodesis 0 Degree Locking Collar...
The Issue: There is a potential dry blast irregularity on the locking collar screws...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WipeEssentials Wet Wipes (benzalkonium chloride 0.13%) Recalled by Diamond...
The Issue: CGMP Deviations: finished products were manufactured with poor quality water.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ACURE Recalled by Diamond Wipes International, Inc. Due to CGMP Deviations:...
The Issue: CGMP Deviations: finished products were manufactured with poor quality water.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PR4100 Microplate Reader US Recalled by Bio-Rad Laboratories Inc Due to The...
The Issue: The connector of the power supply was capable of fitting other components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T2100 Micro flex Drive Treadmill Recalled by GE Medical Systems Ultrasound &...
The Issue: A performance issue with customer owned spare parts, T2100 Microflex drive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bivona¿ Tracheostomy Tube Tracheostomy Tubes Recalled by Smiths Medical ASD...
The Issue: Carton labeling is printed with "Sterile" indicated labeling, however the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Retractor f/Sciatic Nerve Recalled by Synthes (USA) Products LLC Due to...
The Issue: There is a potential for microspores to form on the hollow handle of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.