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Recall Observatory FDA recall evidence

Device product

Bard(R) Premature Infant Feeding tube, ENFit(TM), REF EN0036430 Product Usage: BARD(R) Nasogastric Sump Tubes with ENFit(TM) connector are intended to be used for: Decompression of stomach by suction or aspiration of gastric contents Short-term administration of term tube feeding, lavage fluid and medications Feeding Tubes with the ENFit(TM) Connector are made of a smooth plastic with a two-eyed tube used for nasogastric feeding of neonates, infants and adults as well as diagnostic and therapeutic aspiration. These products are sold single-use, sterile. The Feeding Tube with the ENFit(TM) connector provides a way to reduce the risk of enteral device misconnections. The ENFit(TM) connector: Addresses patient side connections between feeding tubes, administration sets, medication, flush and bolus feeding syringes, and other enteral devices. Does not allow connectivity with any other connector for any other clinical use.

Z-1357-2018

February 27, 2018

Class II

Product summary

Firm
C.R. Bard, Inc.
Event
Event 79507
Status
Terminated
Classification
Class II
Quantity
4800 units
Official record key
device-enforcement:Z-1357-2018

Official wording

Reason: BMD has identified that the product code/lot number combination identified above may have ineffectively fused tubing and ENFit(TM) connector.

Code information: Lot Numbers: NGBN2862, NGAXX217, NGAVX225

Distribution pattern: US Nationwide Distribution

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    BMD has identified that the product code/lot number combination identified above may have ineffectively fused tubing and ENFit(TM) connector.