Reported Jun 5, 2019 · Terminated
RUSCH LASERTUBE (Rubber), Order No. : 102004-000050, REF 102004, SIZE I.D. mm 5,0
Teleflex Medical
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 Medical · 3015 Carrington Mill Blvd · Morrisville, NC · 27560-5437
Is this the product you have?
RUSCH LASERTUBE (Rubber)Order No. : 102004-000050REF 102004SIZE I.D. mm 50
- Lot codes and dates
- Lot Numbers
163 of 163 codes
141511416114171142011421114231142611427114291144511446114491145111504115081150911510115131151611520115211152211524115251153611538115391154111543115441154611549115501160411605116061160811609116111161211614116161161711619116201162211623116241162511626116281162911630116351163611637116381163911640116421
- Lot Numbers
- Amount recalled
- 5995 units
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Where it was sold
- Nationwide
Why it was recalled
The firm received reports indicating that the laser guard foil partially separated and/or slightly detached at the edges.
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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