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. 2,723 recalls have been distributed to Florida in the last 12 months.
Showing 23241–23260 of 30,686 recalls
Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip Recalled by...
The Issue: Incorrectly packaged with a 90 degree bend at the distal tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HYDRO-TEMP(R) Neonatal Temperature Skin Sensor Recalled by DeRoyal...
The Issue: DeRoyal manufactured four lots of HNICU-32, Hydro-Temp(R) Neonatal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip 14.5 Fr/Ch (4.8mm)...
The Issue: Incorrectly packaged with a 90 degree bend at the distal tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SSS Reprocessed Zimmer Recalled by Stryker Sustainability Solutions Due to...
The Issue: It was reported that packaging was not properly sealed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision Chronic Catheter Kit Symmetrical Tip Recalled by...
The Issue: Incorrectly packaged with a 90 degree bend at the distal tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome" Chronic Catheter Kit Symmetrical Tip Recalled by Covidien LLC...
The Issue: Incorrectly packaged with a 90 degree bend at the distal tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Taut Intraducers 10/BX7.5 FR 3.5 Recalled by Teleflex Medical Due to The...
The Issue: The defective component can cause gas leakage through the device. This can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Recalled by Philips Electronics...
The Issue: The following MRx software issue has been identified: MRx model M3535A with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neptune Plus Recalled by TZ Medical Inc. Due to The IFU of the Neptune Plus...
The Issue: The IFU of the Neptune Plus Pads, does not match that submitted in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovoCut Suture Manager Recalled by Ceterix Orthopedics, Inc. Due to The...
The Issue: The NovoCut Suture Manager device may cut the suture during knot tensioning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access CEA Assay Recalled by Beckman Coulter Inc. Due to Beckman Coulter is...
The Issue: Beckman Coulter is recalling the Access CEA reagent packs because they were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Two-stage and three-stage I.V. poles are shipped as an optional Recalled by...
The Issue: It was identified by a customer complaint that some I.V. poles were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspiration Ventilator System Recalled by Event Medical LTD Due to A...
The Issue: A component on the systems power board can fail in a manner which can cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartSite Extension Set Recalled by CareFusion 303, Inc. Due to CareFusion...
The Issue: CareFusion is recalling the SmartSite Extension Set due to disconnection and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RotaWire Elite and wireClip Torquer Recalled by Boston Scientific...
The Issue: Boston Scientific is recalling its recently released RotaWire Elite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RotaWire Elite and wireClip Torquer Recalled by Boston Scientific...
The Issue: Boston Scientific is recalling its recently released RotaWire Elite...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: miraDry System consisting of the MD4000-MC Console Recalled by Miramar Labs,...
The Issue: Update to labeling for the miraDry Console to remind users to only use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Small Notch Titanium Reconstructive Plate set (SNTRP). Ti...
The Issue: The Synthes SNTRP set was released for sale as a Trauma product in 1996 with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shuttle Select Slip-Cath Catheter. Angiographic catheter. For use in...
The Issue: Reports of catheter tip splits and or separation. Loss of device function,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cyberonics Vagus Nerve Stimulator (VNS) Therapy AspireSR Generator Recalled...
The Issue: Certain Model 106 Pulse Generators demonstrate delays in sensing during use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.