Home / Recalls / Medical Devices
Becton Dickinson & Company recalls BD Posiflush SF Saline Flush Syringe (US Distributed Catalog 306553), UDI 50382903065535
Recalled May 27, 2020 · FDA recall Z-2065-2020 · Becton Dickinson &
Hazard
This product has been confirmed to exhibit holes in the packaging, which impacts package integrity and potentially compromises a sterile field. · FDA Class II
Units
16,099,310 units
Sold at
Nationwide domestic distribution. Foreign distribution to Austria, Belgium, Denmark, Finland, France, Germany, Italy, Netherlands, Norway, Portugal, Spain, Sweden, Switzerland, UK, Australia, Canada, Mexico, Malaysia, New Zealand
Description
This product has been confirmed to exhibit holes in the packaging, which impacts package integrity and potentially compromises a sterile field.
Product
BD Posiflush SF Saline Flush Syringe (US Distributed Catalog 306553), UDI 50382903065535
Manufacturer(s)
Becton Dickinson & Company
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →