medical MODERATE Updated 2023-07-12

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

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Recalled Product

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

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Hazard / Issue

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

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: 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

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

Looking for a safe alternative?

Search Amazon for Pilling O'REILLY ESOPHAGEAL RETRACTOR, →

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View official government recall

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