TELEFLEX LLC: Medical Device Recall in 2023 - (Recall #: Z-2095-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: May 25, 2023

Date Posted: July 12, 2023

Recall Number: Z-2095-2023

Event ID: 92416

Reason for Recall:

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

Status: Ongoing

Product Quantity: 365 units

Code Information:

Lot Numbers: B5, B6, B9, C6, C7, D2, D6, E5, E9, F2, F3, F5, F8, G4, G5, G9, I3, I4, I7, I8, J2, J3, K4, K5, K7, K8, L2, L9, O2, Q0, R2, S2, U0, V2, W1

Distribution Pattern:

Nationwide and Australia, Canada, S. Korea, Singapore

Voluntary or Mandated:

Voluntary: Firm initiated