FDAFebruary 23, 2022device

(a) CareFusion Snowden-Pencer Plastics, Endoplastic Endoscope 10 mm, 30 degrees 7", 17.5 cm, Catalog #88-5910; (b) CareFusion Snowden-Pencer Plastics, Endoplastic Endoscope 5 mm, 30 degrees 7", 17.5 cm, Catalog #88-5920; (c) CareFusion Snowden-Pencer MIS, Endoplastic Fitting, Storz Scope, Catalog...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The finished device package did not contain the IFU.

What to do

FDA enforcement status: Terminated

Brands named

carefusion 2200carefusion

UPCs

10885403153341108854031533581088540315531410885403155321

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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(a) CareFusion Snowden-Pencer Plastics, Endoplastic Endoscope 10 mm, 30 degrees 7", 17.5 cm, Catalog #88-5910; (b) CareFusion Snowden-Pencer Plastics, Endoplastic Endoscope 5 mm, 30 degrees 7", 17.5 cm, Catalog #88-5920; (c) CareFusion Snowden-Pencer MIS, Endoplastic Fitting, Storz Scope, Catalog... — Recall Details · AllClear