BD Posiflush SF Saline Flush Syringe (US Distributed Catalog 306553), UDI 50382903065535
Reported: May 27, 2020 Initiated: April 16, 2020 #Z-2065-2020
Product Description
BD Posiflush SF Saline Flush Syringe (US Distributed Catalog 306553), UDI 50382903065535
Reason for Recall
This product has been confirmed to exhibit holes in the packaging, which impacts package integrity and potentially compromises a sterile field.
Details
- Recalling Firm
- Becton Dickinson & Company
- Units Affected
- 16,099,310 units
- Distribution
- 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
- Location
- Franklin Lakes, NJ
Frequently Asked Questions
What product was recalled? ▼
BD Posiflush SF Saline Flush Syringe (US Distributed Catalog 306553), UDI 50382903065535. Recalled by Becton Dickinson & Company. Units affected: 16,099,310 units.
Why was this product recalled? ▼
This product has been confirmed to exhibit holes in the packaging, which impacts package integrity and potentially compromises a sterile field.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on May 27, 2020. Severity: Moderate. Recall number: Z-2065-2020.
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