Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Pilling O'REILLY ESOPHAGEAL RETRACTOR Recalled by TELEFLEX LLC Due to There are incomplete pre-cleaning instructions within the Instructions...
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 TELEFLEX LLC directly.
Affected Products
Pilling O'REILLY ESOPHAGEAL RETRACTOR, REF 381801A; ENT retractor
Quantity: 365 units
Why Was This Recalled?
There are incomplete pre-cleaning instructions within the Instructions for Use (IFU).
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About TELEFLEX LLC
TELEFLEX LLC has 139 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report