TELEFLEX LLC Pilling O'REILLY ESOPHAGEAL RETRACTOR, REF 381801A; ENT retractor Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Pilling O'REILLY ESOPHAGEAL RETRACTOR, REF 381801A; ENT retractor
Brand
TELEFLEX LLC
Lot Codes / Batch Numbers
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
Products Sold
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
TELEFLEX LLC is recalling Pilling O'REILLY ESOPHAGEAL RETRACTOR, REF 381801A; ENT retractor due to There are incomplete pre-cleaning instructions within the Instructions for Use (IFU).. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
There are incomplete pre-cleaning instructions within the Instructions for Use (IFU).
Recommended Action
Per FDA guidance
Teleflex issued an URGENT MEDICAL DEVICE NOTIFICATION to its consignees on 05/25/2023 by Fed Ex 2nd day delivery. The notice explained the problem, the risk to health, and requested the following actions be taken: Medical facilities are to check the facilities for the product and place a copy of the notice with it. Distributors are directed to check for the product and place a copy of the notice with the product, and notify all customers to whom the product has been distributed.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026