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 20561–20580 of 30,686 recalls
Recalled Item: OR Table Recalled by Trumpf Medical Systems, Inc. Due to Trumpf has...
The Issue: Trumpf has identified six incidents of pinched cables.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquilion Prime TSX-303A Aquilion PRIME is a multislice helical CT Recalled...
The Issue: Toshiba American Medical Systems (TAMS) is recalling the Aquilion CT system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SONNET Mini Battery Pack CableProduct Usage: The SONNET Mini Battery...
The Issue: Unit Defect: Firm inspection revealed units did not have the compartment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gammex Non-Latex Sensitive Neoprene Surgical Gloves Ansell Lanka (pvt) Ltd....
The Issue: Ansell Healthcare Products is initiating a voluntary recall involving 15...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Ostase QC Recalled by Beckman Coulter Inc. Due to Beckman Coulter has...
The Issue: Beckman Coulter has determined that the Access Ostase Calibrator and Access...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Ostase Calibrators Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter has determined that the Access Ostase Calibrator and Access...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FMsealer Open Shears. Model FM3001 Recalled by Domain Surgical, Inc. Due to...
The Issue: Domain Surgical, Inc. announces a voluntary field action for the FMsealer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVION S250 Product Usage: Proton Radiation Therapy System Recalled by...
The Issue: Recovery of Incorrect Isocenter -operational change
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi-Med Single Lumen Catheters sold in Centurion convenience kits. The...
The Issue: The kits contain Multi-Med Single Lumen Catheters that have a potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 560 Hematology Systems Recalled by Siemens Healthcare Diagnostics,...
The Issue: Siemens is investigating an issue which may cause an incorrect result to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Force Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...
The Issue: Siemens is providing software update version VA50A_SP3 to address the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Recalled by Merge Healthcare, Inc. Due to A product issues happens for...
The Issue: A product issues happens for RF projection images. If user measures on RF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVION S250 Product Usage: Proton Radiation Therapy System Recalled by...
The Issue: Software defect:2D projection of contours in Verity. The defect causes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nordson Micromedics FibriJet Endoscopic Catheter Introducer Recalled by...
The Issue: The sterile packaging may contain small channels in the seal of the pouch,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition AS system Recalled by Siemens Medical Solutions USA, Inc...
The Issue: Hardware issue that may expose the User to a potential risk for serious...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultroid Procedure Pack including the Ultroid Sterile Disposable Probes....
The Issue: Products are not designed, qualified, manufactured, and/or managed under a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultroid Hemorrhoid Management Systems 110/220 VAC and procedures kit...
The Issue: Products are not designed, qualified, manufactured, and/or managed under a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Offset Reamer Handle Recalled by Greatbatch Medical Due to On June 14, 2016,...
The Issue: On June 14, 2016, Greatbatch discovered a significant increase in the number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultroid Sterile Disposable Probes sold individually Recalled by Ultroid...
The Issue: Products are not designed, qualified, manufactured, and/or managed under a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: A problem can occur with the small light marker windows, used for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.