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FDA (Device enforcement)Recalled 2019-07-17closedclass ii

Becton Dickinson & Co.: Kit BD Max Cdiff EU; Catalog # 442555

Is my product affected?

Kit BD Max Cdiff EU; Catalog # 442555

  • UPC 00382904425555

Check against the official notice below — it lists the full affected range.

What happened

Becton Dickinson & Co. is recalling the BD MAX Cdiff EU Kit (Catalog # 442555) because the foil bags containing extraction tubes for BD MAX Reagent products may not have been sealed properly. Only 4 units were affected, specifically those from Lot # 9127912. The product was distributed across multiple U.S. states (including Alabama, Arizona, California, Florida, New York, Texas, and others) as well as internationally in countries such as Australia, Canada, Japan, Mexico, and Singapore.

The recall notice does not specify a remedy or corrective action that affected consumers should take.

Written by software from the official notice below. Not reviewed by a lawyer.

Hazard

The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.

Details from the source

Reason for recall: The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly. Distribution: AL, AR, AZ, CA, CO, CT, FL, GA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MT, NC, NH, NJ, NM, NV, NY, OH, OR, PA, PR, RI, SC, TN, TX, VA, WA, WI, WV Worldwide: Australia, Belgium, Brazil, Canada, Chile, China, Hong Kong, Japan, Korea, Mexico, Singapore, Taiwan Quantity: 4 units Lot/code info: Lot # 9127912 ; UDI (GTIN, DI+PI): (01)00382904425555 (17)201114(10)9127912(30)1

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.

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