Pilling O'reilly Esophageal Retractor recall
Pilling O'REILLY ESOPHAGEAL RETRACTOR, REF 381801A; ENT retractor
Why was Pilling O'reilly Esophageal Retractor recalled?
There are incomplete pre-cleaning instructions within the Instructions for Use (IFU).
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
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
- Product
- Pilling O'REILLY ESOPHAGEAL RETRACTOR, REF 381801A; ENT retractor
- Recalling firm
- TELEFLEX LLC
- Quantity
- 365 units
- Distribution
- Nationwide and Australia, Canada, S. Korea, Singapore
- Recall date
- July 12, 2023
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)