Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
(a) CareFusion Snowden-Pencer Plastics Recalled by Carefusion 2200 Inc Due to The finished device package did not contain the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Carefusion 2200 Inc directly.
Affected Products
(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 #88-9808; and (d) CareFusion Snowden-Pencer MIS, Endoplastic Fitting, Wolf Scope, Catalog #88-9809.
Quantity: 152 units
Why Was This Recalled?
The finished device package did not contain the IFU.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Carefusion 2200 Inc
Carefusion 2200 Inc has 112 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report