Reported May 31, 2017 · Terminated
PE CONNECTOR 3/8 Y 20/BX, Sterile, Single use, Product Usage: Catheter Connector/Accessory
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 · 2917 Weck Dr · Research Triangle Park, NC · 27709-0186
Is this the product you have?
- PE CONNECTOR 3/8 Y 20/BX, Sterile, Single use
- Product UsageCatheter Connector/Accessory
- Lot codes and dates
- Product CodePE101
- Lot numbers
02A110007802A140341802B090048402B120133202C100232702C110125202D080266902D080396702D110133302D110197502D120149202E090090902F080027902F110176502G080204602G090010602G090285802G130227702H090165202H090260302H110393902K090056802K100026902K100199702K110312302K130103302L070146402L090152102L100257802L100352774A160169674C160105774E160094274E160282574F140127074H150137874J1502624 & 74L1500554
- Amount recalled
- 19,043 units in total
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Where it was sold
- Nationwide
Why it was recalled
Labeling: The expiration date is not stated on the labeling, there is a potential for expired product to be used.
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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