Reported May 31, 2017 · Terminated
PE CONNECTOR 3/8 STRAIGHT 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 STRAIGHT 20/BX, Sterile, Single use
- Product UsageCatheter Connector/Accessory
- Lot codes and dates
- Product CodePE100
- Lot numbers
02F080111502F090185902G080274802G090081402H090019202K090056702L090016302M090100674A160169574G150013774G1502714 & 74M1400489
- 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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