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. 1,897 recalls have been distributed to Florida in the last 12 months.
Showing 38641–38660 of 55,837 recalls
Recalled Item: USE (Ebony) PTA .014" rapid exchange (RX) Peripheral Dilatation Catheter....
The Issue: Product may kink during use rendering the product unusable.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplexa Flu A/B & RSV Direct (MOL2650) with Direct Amplification Disc...
The Issue: Focus Diagnostics is recalling the Direct Amplification Discs (DAD) supplied...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intra operative MRI Systems: Neuro II-SE Recalled by Deerfield Imaging Due...
The Issue: Emergency helium venting lines (i.e. quench lines) may not have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Insertion Tray Recalled by Arrow International, Inc., Division...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra 8 IAB: 8Fr 40cc Recalled by Arrow International, Inc., Division of...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultra 8 IAB: 8Fr 30cc Recalled by Arrow International, Inc., Division of...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation Therapy Treatment Planning System Stand-alone Software 3.0...
The Issue: A software issue with editing tools that use the left mouse button held...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RediGuard IAB: 7Fr 30cc Recalled by Arrow International, Inc., Division of...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraFlex IAB: 7.5Fr 30cc Recalled by Arrow International, Inc., Division of...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FiberOptix Ultra 8 IAB: 8Fr 30cc The Arrow¿ IAB is Recalled by Arrow...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: eValueMed Infant Transport Mattress 301-1015 Recalled by Philips Electronics...
The Issue: eValueMed Infant Heel Warmers and eValueMed Infant Transport Mattresses bear...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: evaluemed Infant Heel Warmer 301-1223 Recalled by Philips Electronics North...
The Issue: eValueMed Infant Heel Warmers and eValueMed Infant Transport Mattresses bear...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraFlex IAB: 7.5Fr 40cc Recalled by Arrow International, Inc., Division of...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Insertion Tray Recalled by Arrow International, Inc., Division...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplexa Group A Strep Direct (MOL2850) with Direct Amplification Disc...
The Issue: Focus Diagnostics is recalling the Direct Amplification Discs (DAD) supplied...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FiberOptix Ultra 8 IAB: 8Fr 40cc Recalled by Arrow International, Inc.,...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplexa HSV 1&2 Direct (MOL2150) with Direct Amplification Disc (MOL1451...
The Issue: Focus Diagnostics is recalling the Direct Amplification Discs (DAD) supplied...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult Robitussin PEAK COLD Cough & Chest Congestion DM Liquid Recalled by...
The Issue: Labeling: Label Mix-Up
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TEARS Naturale FREE (dextran 70 and hypromellose 2910) lubricant eye drops...
The Issue: Lack of Assurance of Sterility: Some single-use vials may be filled with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dimension clinical chemistry system Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics has received customer complaints regarding QC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.