Reported May 27, 2020 · Terminated
BD Posiflush SF Saline Flush Syringe (US Distributed Catalog 306553), UDI 50382903065535
Becton Dickinson & Company
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Becton Dickinson & Company · 1 Becton Dr · Franklin Lakes, NJ · 07417-1815
Is this the product you have?
- BD Posiflush SF Saline Flush Syringe (US Distributed Catalog 306553), UDI 50382903065535
- Lot codes and dates
- Lots
83539529011582901787590246769045702906099990797169127571914352991565959163601
- Lots
- Amount recalled
- 16,099,310 units
This recall covers 9 products
The agency filed one notice per product. You are reading one of them; the other 8 are below.
Where it was sold
- Nationwide
Why it was recalled
This product has been confirmed to exhibit holes in the packaging, which impacts package integrity and potentially compromises a sterile field.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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