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Teleflex Medical recalls PE CONNECTOR 3/8 STRAIGHT 20/BX, Sterile, Single use, Product Usage: Catheter Connector/Accessory
Recalled May 31, 2017 · FDA recall Z-2127-2017 · Teleflex Medical
Hazard
Labeling: The expiration date is not stated on the labeling, there is a potential for expired product to be used. · FDA Class II
Units
19,043 units in total
Sold at
Worldwide Distribution - U.S. Nationwide. Foreign consignees: Australia, Canada, China, Columbia, India, San Salvador, Singapore and South Korea.
Description
Labeling: The expiration date is not stated on the labeling, there is a potential for expired product to be used.
Product
PE CONNECTOR 3/8 STRAIGHT 20/BX, Sterile, Single use, Product Usage: Catheter Connector/Accessory
Manufacturer(s)
Teleflex Medical
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →