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. 2,710 recalls have been distributed to Florida in the last 12 months.
Showing 26341–26360 of 30,686 recalls
Recalled Item: Apex Arc Hip Stem Recalled by Omnilife Science Inc. Due to Staining on hip...
The Issue: Staining on hip implant.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anspach Pneumatic and Electric Motor Systems. Intended for cutting and...
The Issue: Several attachments and handpieces failed to meet the expected sterility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Devon Supine Recalled by Covidien LLC Due to Straps may separate from the...
The Issue: Straps may separate from the foam pad.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MACROLYTE Premie Dispersive Electrode Recalled by ConMed Corporation Due to...
The Issue: ConMed Corporation has received complaints regarding sparking, no output and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G7 Acetabular System Positioning Guide Rod Recalled by Biomet, Inc. Due to...
The Issue: Guide rod may fracture during impaction of the acetabular shell and be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G7 Acetabular System Positioning Guide Post Recalled by Biomet, Inc. Due to...
The Issue: Guide rod may fracture during impaction of the acetabular shell and be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Luxurian. These include all products labeled as UltraSlim Recalled by...
The Issue: Marketing without marketing clearance or approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultraslim. These include all products labeled as UltraSlim Recalled by...
The Issue: Marketing without marketing clearance or approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens LANTIS System Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: There is a potential risk when using LANTIS OIS System client software with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Photonica Light Modulator. These include all products labeled as UltraSlim...
The Issue: Marketing without marketing clearance or approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Visitec Anterior Chamber Cannula Recalled by Beaver-Visitec International...
The Issue: Contains a sharp tip needle when the product should contain a blunt tip cannula
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: All Philips Ingenia Recalled by Philips Medical Systems, Inc. Due to In...
The Issue: In spine clinical workflows, cross lines may be used to determine the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips XRE Recalled by Philips Healthcare Informatics, Inc. Due to When...
The Issue: When using XIRIS Rio version (8.1.50.0) in conjuncture with iSite PACS a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVOCATE Redi-Code+ BMB-BA006A Blood Glucose test strips Product Usage: The...
The Issue: "Advocate Redi-Code + BMB-BA006A Blood Glucose test strips" are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Horizon Medical Imaging It is a medical image and information Recalled by...
The Issue: The firm has identified a software issue which may cause a discrepancy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Triage¿ D-Dimer Test PN 98100 Recalled by Alere San Diego, Inc. Due to...
The Issue: Alere initiated this recall because a limited number of Alere Triage¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kenex Radiation Shield and surgical lamps installed with GE Healthcare...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Triathlon Tritanium Patella Inserter Recalled by...
The Issue: Tritanium Patella Inserter Instrument fracture during implantation. .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PATH(R) THREAD CUP ADAPTOR Recalled by Microport Orthopedics INC. Due to...
The Issue: Difficulty removing the cup adaptor from the impaction handle during surgery
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Robotic Arm Interactive Orthopedic System (RIO) Recalled by Mako Surgical...
The Issue: Revision of the field manual
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.