Reported Aug 28, 2019 · Terminated
Kit BD Max MRSA; Catalog # 442953
Becton Dickinson & Co.
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 & Co. · 7 Loveton Cir · Sparks, MD · 21152-9212
Is this the product you have?
- Kit BD Max MRSA; Catalog # 442953
- Lot codes and dates
- Lot # 9071522; UDI (GTIN, DI+PI): (01)00382904429539 (17)191219(10)9071522(30)1
- Exp12/19/2019
- Amount recalled
- 176 units
This recall covers 19 products
The agency filed one notice per product. You are reading one of them; the other 18 are below.
6 more are in the archive.
Where it was sold
Why it was recalled
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
This product could cause temporary or reversible health problems — stop using it.
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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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