Reported May 31, 2017 · Terminated

PE CONNECTOR 5 IN 1 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 5 IN 1 20/BX, Sterile, Single use
  • Product UsageCatheter Connector/Accessory
Lot codes and dates
  • Product CodePE102
  • Lot numbers
    • 02A1101041
    • 02B1102552
    • 02C1001258
    • 02C1003795
    • 02C1101253
    • 02C1104114
    • 02D0802670
    • 02D0803968
    • 02D1000682
    • 02D1002136
    • 02D1101334
    • 02E1001502
    • 02E1100384
    • 02F0800281
    • 02F1000667
    • 02F1002368
    • 02F1101766
    • 02F1102607
    • 02F1103754
    • 02G1000322
    • 02G1001538
    • 02H0801670
    • 02H0803375
    • 02H1000732
    • 02H1103023
    • 02H1103940
    • 02J1000236
    • 02J1001515
    • 02J1002609
    • 02J1003237
    • 02J1101139
    • 02J1102143
    • 02K1000270
    • 02K1001993
    • 02K1100519
    • 02K1103124
    • 02K1301613
    • 02L0701463
    • 02L0701958
    • 02L0702675
    • 02L1000763
    • 02M0700783
    • 02M1001319
    • 74A1600225
    • 74A1600226
    • 74B1601947
    • 74B1601948
    • 74D1600917
    • 74F1401859
    • 74F1502294
    • 74F1502573
    • 74F1602371
    • 74H1601152
    • 74J1601641
    • 74K1501590 & 74L1500555
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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Jan 27, 2020 · Data as of Sep 19, 6:00 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.