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. 2,754 recalls have been distributed to Florida in the last 12 months.
Showing 21061–21080 of 30,686 recalls
Recalled Item: Glucose Tolerance Beverage- Orange 50 gram Concentration Recalled by Azer...
The Issue: Out of Specification Microbiological test results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WECK¿ Horizon" Manual-Load Ligating Clip Applier Recalled by Teleflex...
The Issue: Misbranded: Incorrect etching on the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Cranial Access Kits Recalled by Integra LifeSciences Corp. d.b.a....
The Issue: Integra LifeSciences has been notified of a medical device recall by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS IMMULITE/IMMULITE 1000 Systems Rubella IgM (RUM) Recalled by Siemens...
The Issue: Siemens received multiple customer complaints indicating an increase in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tego Connector Recalled by ICU Medical, Inc. Due to ICU Medical Inc. has...
The Issue: ICU Medical Inc. has identified a potential risk of leaking with certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Straight Ventricular Catheter F8 Recalled by Integra LifeSciences...
The Issue: During final sampling inspection, one of the lots was discovered with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Ventricular Catheter Accessory Kit Recalled by Integra LifeSciences...
The Issue: During final sampling inspection, one of the lots was discovered with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Lumbar Drainage Set Recalled by Integra LifeSciences Corp. Due to...
The Issue: During final sampling inspection, one of the lots was discovered with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Drainage Accessory Kits Recalled by Integra LifeSciences Corp. Due...
The Issue: During final sampling inspection, one of the lots was discovered with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CUSA Dissectron Fingertip Laparoscopic Cannula Recalled by Integra...
The Issue: During final sampling inspection, one of the lots was discovered with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integral Lumbar Drainage Set Recalled by Integra LifeSciences Corp. Due to...
The Issue: During final sampling inspection, one of the lots was discovered with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sertera Biopsy Device Recalled by Hologic, Inc Due to Incorrect label on the...
The Issue: Incorrect label on the Sertera Biopsy Kit
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The EKOS cart has the catalog number 700-60101. The EKOS Recalled by EKOS...
The Issue: Casters on the EKOS carts may be missing washers which can cause premature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panoramic X-ray Model PC-1000 Recalled by Panoramic Rental Corp. Due to...
The Issue: Panoramic Corporation is performing a voluntary Medical Device Correction on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System Used to make treatment plans for patients Recalled by...
The Issue: In a specific workflow where contours are edited (enlarged, moved, copied,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HexaPOD evo RT System Product Usage: The intended use of Recalled by Elekta,...
The Issue: Potentially unrecognized incorrect position of the treatment couch in 3D...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Drape Recalled by NOVADAQ TECHNOLOGIES INC. Due to Novadaq is...
The Issue: Novadaq is informing SK6000 PAQ users that a pinhole through the drape pouch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sagittal Blade 18.0X0.97X90MM Recalled by Stryker Instruments Div. of...
The Issue: Stryker Instruments is voluntarily recalling the Sagittal Blade...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD) Recalled by HeartWare, Inc Due to...
The Issue: Foreign material found within the driveline connector of the HVAD Pump that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pathfast D-Dimer Recalled by Lsi Medience Corporation Due to Two complaints...
The Issue: Two complaints were received about decrease in sensitivity (control value...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.