medical MODERATE Updated 2017-05-31

Teleflex Medical recalls PE CONNECTOR 5 IN 1 20/BX, Sterile, Single use, Product U

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Recalled Product

PE CONNECTOR 5 IN 1 20/BX, Sterile, Single use, Product Usage: Catheter Connector/Accessory

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Hazard / Issue

Labeling: The expiration date is not stated on the labeling, there is a potential for expired product to be used.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Product Code: PE102, 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.

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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