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 12041–12060 of 55,837 recalls
Recalled Item: Prismaflex HF20 Set (product code 109841). For use in providing Recalled by...
The Issue: Within the current Prismaflex set IFU (instructions for use), there is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex ST Set: ST60 (product code 107643) Recalled by Baxter Healthcare...
The Issue: Within the current Prismaflex set IFU (instructions for use), there is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex M Set: M60 (product code 106696) Recalled by Baxter Healthcare...
The Issue: Within the current Prismaflex set IFU (instructions for use), there is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex M Set: M150 (product code 109990). For use in Recalled by Baxter...
The Issue: Within the current Prismaflex set IFU (instructions for use), there is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prismaflex HF Set: HF1000 (product code 107140) Recalled by Baxter...
The Issue: Within the current Prismaflex set IFU (instructions for use), there is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lisinopril Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to Foreign...
The Issue: Presence of Foreign Substance: Foreign material (metal piece) embedded in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NovoTHOR Gen 2.5 Regular whole body red light therapy bed Recalled by Thor...
The Issue: Failure of ball stud components causing the gas strut on one side to detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovoTHOR Gen 2.0 whole body red light therapy bed Recalled by Thor...
The Issue: Failure of ball stud components causing the gas strut on one side to detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G041 POD Recalled by Thor Photomedicine Ltd Due to Failure of ball stud...
The Issue: Failure of ball stud components causing the gas strut on one side to detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovoTHOR Gen 2.5 XL whole body red light therapy bed Recalled by Thor...
The Issue: Failure of ball stud components causing the gas strut on one side to detach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE ADLT BLOOD CLUTURE COLLECT KIT Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE PHERIPHERAL BLOOD CULTURE DRAW Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE PRE-OP CHG BATHING KIT Reorder #: P164756 Recalled by MEDLINE...
The Issue: Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE BLOOD CLUTURE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield...
The Issue: Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE 24 BLOOD CLUTURE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield...
The Issue: Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product/Part: MitraClip XTR Clip Delivery System US/CDS0601-XTR Recalled by...
The Issue: An increase in clip locking malfunctions, Establish Final Arm Angle and Clip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product/Part: MitraClip NTR Clip Delivery System US/CDS0601-NTR Recalled by...
The Issue: An increase in clip locking malfunctions, Establish Final Arm Angle and Clip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product/Part: MitraClip G4 CDS NT REPAIR-MR Clinical/CDS0704-NT Recalled by...
The Issue: An increase in clip locking malfunctions, Establish Final Arm Angle and Clip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Full Kit Pulset 3cc Syringe 23g x 1 Safety Tip 25u BH Recalled by SunMed...
The Issue: The kits are being recalled due to a lack of sterility of a spare needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: THERMOCOOL SMARTTOUCH SF Bi-Directional Navigation Catheter Recalled by...
The Issue: Manufacturing error resulted in potential contamination of Bi-Directional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.