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Teleflex, and Arrow International, Recall Pressure Injectable Catheter Kits for Mislabeling

Teleflex, and its subsidiary Arrow International, are recalling the Pressure Injectable Catheter Kits due to mislabeling regarding the presence of chlorhexidine in these products. The product code and product name are incorrectly listed as non-coated on the lids of the affected Pressure Injectable Catheter Kits. However, the banner card correctly lists the product code and product name as chlorohexidine coated.

The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.

Questions?

If you have questions about this recall, contact Teleflex and its subsidiary, Arrow International Customer Service by phone at 1-866-396-2111 or by emailing recalls@teleflex.com.