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
| Model / number | Barcodes | Product as published |
|---|---|---|
88-5910 | 10885403153341 | (a) - Lot numbers C17XRD and K17XRD, UDI 10885403153341 |
88-5920 | (b) - Lot numbers XRDX02, XRDZ07, K17XRD, C18XRD, G18XRD, C19XRD, D20XRD, G20XRD, J19XRD, K19XRD | |
| — | 10885403153358 | UDI 10885403153358 |
88-9808 | (c) - Lot numbers XRDV09, G20XRD, 864909 | |
| — | 10885403155314 | UDI 10885403155314 |
88-9809 | and (d) - Lot numbers XRDV09, XRDV10, XRDX06, B18XRD, D18XRD, G20XRD | |
| — | 10885403155321 | UDI 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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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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