Reported Jul 12, 2023 · Ongoing
Pilling O'REILLY ESOPHAGEAL RETRACTOR, REF 381801A; ENT retractor
Teleflex LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: TELEFLEX LLC · 3015 Carrington Mill Blvd · Morrisville, NC · 27560-5437
Is this the product you have?
- Pilling O'REILLY ESOPHAGEAL RETRACTOR, REF 381801A; ENT retractor
- Lot codes and dates
- Lot Numbers
B5B6B9C6C7D2D6E5E9F2F3F5F8G4G5G9I3I4I7I8J2J3K4K5K7K8L2L9O2Q0R2S2U0V2W1
- Lot Numbers
- Amount recalled
- 365 units
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
- Nationwide
Why it was recalled
There are incomplete pre-cleaning instructions within the Instructions for Use (IFU).
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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