Reported Apr 6, 2022 · Terminated

(a) CareFusion Snowden-Pencer Plastics, Endoplastic Endoscope 10 mm, 30 degrees 7", 17.5 cm, Catalog #88-5910; (b)…

Carefusion 2200 Inc.

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: Carefusion 2200 Inc · 75 N Fairway Dr · Vernon Hills, IL · 60061-1845

Is this the product you have?

7 of 7 products

Products covered by this recall
Model / numberBarcodesProduct as published
88-591010885403153341(a) - Lot numbers C17XRD and K17XRD, UDI 10885403153341
88-5920(b) - Lot numbers XRDX02, XRDZ07, K17XRD, C18XRD, G18XRD, C19XRD, D20XRD, G20XRD, J19XRD, K19XRD
10885403153358UDI 10885403153358
88-9808(c) - Lot numbers XRDV09, G20XRD, 864909
10885403155314UDI 10885403155314
88-9809and (d) - Lot numbers XRDV09, XRDV10, XRDX06, B18XRD, D18XRD, G20XRD
10885403155321UDI 10885403155321.
Amount recalled
152 units

Where it was sold

Why it was recalled

The finished device package did not contain the IFU.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated May 2, 2023 · Data as of Sep 19, 5:35 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.