TELEFLEX LLC recalls Pilling O'REILLY ESOPHAGEAL RETRACTOR, REF 381801A; ENT retractor

Recalled July 12, 2023 · FDA recall Z-2095-2023 · TELEFLEX

Hazard

There are incomplete pre-cleaning instructions within the Instructions for Use (IFU). · FDA Class II

Units

365 units

Sold at

Nationwide and Australia, Canada, S. Korea, Singapore

Description

There are incomplete pre-cleaning instructions within the Instructions for Use (IFU).

Product

Pilling O'REILLY ESOPHAGEAL RETRACTOR, REF 381801A; ENT retractor

Manufacturer(s)

TELEFLEX LLC

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →