Reported Oct 16, 2019 · Terminated

BD Microtainer SST Part/Catalog No.365967

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 Microtainer SST Part/Catalog No.365967
Lot codes and dates
  • Lot Number/UDI8094573 (01)30382903659679 (17)190630(10)8094573(30)50 (17)190630(10)8094573(30)200 (01)50382903659673 8094575 (01)30382903659679 (17)190630(10)8094575(30)50 (17)190630(10)8094575(30)200 (01)50382903659673 8094578 (01)30382903659679 (17)190630(10)8094578(30)50 (17)190630(10)8094578(30)200 (01)50382903659673 8117697 (01)30382903659679 (17)190731(10)8117697(30)50 (17)190731(10)8117697(30)200 (01)50382903659673 8165883 (01)30382903659679 (17)190831(10)8165883(30)50 (17)190831(10)8165883(30)200 (01)50382903659673 8165884 (01)30382903659679 (17)190831(10)8165884(30)50 (17)190831(10)8165884(30)200 (01)50382903659673 8170911 (01)30382903659679 (17)190831(10)8170911(30)50 (17)190831(10)8170911(30)200 (01)50382903659673 8171861 (01)30382903659679 (17)190831(10)8171861(30)50 (17)190831(10)8171861(30)200 (01)50382903659673 8220937 (01)30382903659679 (17)191031(10)8220937(30)50 (17)191031(10)8220937(30)200 (01)50382903659673 8220938 (01)30382903659679 (17)191031(10)8220938(30)50 (17)191031(10)8220938(30)200 (01)50382903659673 8282848 (01)30382903659679 (17)191231(10)8282848(30)50 (17)191231(10)8282848(30)200 (01)50382903659673 8284571 (01)30382903659679 (17)191231(10)8284571(30)50 (17)191231(10)8284571(30)200 (01)50382903659673 8284574 (01)30382903659679 (17)191231(10)8284574(30)50 (17)191231(10)8284574(30)200 (01)50382903659673
Amount recalled
N/A

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

Why it was recalled

Damaged reservoir may lead to a decreased fill volume causing samples to be insufficient for testing and improper blood-to-additive ratio, potentially producing erroneous results.

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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Aug 6, 2020 · Data as of Sep 19, 5:31 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.