Teleflex Medical recalls INFANT 20/BX, Sterile, Single use Product Usage: Catheter Connector/Accessory
- Recall date
- April 21, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2130-2017
- FDA classification
- Class II
- Brand / firm
- Teleflex Medical
- Sold / distributed
- Worldwide Distribution - U.S. Nationwide. Foreign consignees: Australia, Canada, China, Columbia, India, San Salvador, Singapore and South Korea.
What was recalled
INFANT 20/BX, Sterile, Single use Product Usage: Catheter Connector/Accessory
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