FDAClass IIJuly 10, 2024

WOM Tube Set for lrrlgatlon recall

WOM Tube Set for lrrlgatlon, single-use- Intended to transport irrigation fluid to the patient in endoscopic surgeries. Distr. by Endoscopy Smith &…

Why was WOM Tube Set for lrrlgatlon recalled?

Incorrect transponder data was written on the RFID tags triggers the error message E03, Tube Set lnvalid, may result in a delay of surgery

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

UDI: 04056702003678 Lot Numbers: 4030902, 4030903

Product
WOM Tube Set for lrrlgatlon, single-use- Intended to transport irrigation fluid to the patient in endoscopic surgeries. Distr. by Endoscopy Smith &…
Recalling firm
WOM World Of Medicine AG
Quantity
1700 units
Distribution
US Nationwide distribution.
Recall date
July 10, 2024
Classification
Class II
Status
Ongoing
Agency
FDA (device)
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