PE CONNECTOR 5 IN 1 20/BX, Sterile, Single use, Product Usage: Catheter Connector/Accessory
Class I - DangerousWhat Should You Do?
- Check if you have this product: 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.
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Teleflex Medical
- Reason for Recall:
- Labeling: The expiration date is not stated on the labeling, there is a potential for expired product to be used.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
PE CONNECTOR 5 IN 1 20/BX, Sterile, Single use, Product Usage: Catheter Connector/Accessory
Product Codes/Lot Numbers:
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.
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-2129-2017
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