Atlas FDA

Standard tubing set, Synergetics, Inc., length 10 ft, sterile / EO, 17570. Packed 6 units per box. Manufactured for Syne

FDA device recall Z-0872-2014 · posted 2014-01-30 · Terminated

Recall details

Recalling firm
Synergetics Inc
Reason for recall
Faulty seals on the outer pouch of various, double-pouched, single-use, sterile, ophthalmic devices could result in seal failure.
Action taken
Domestic customers were sent recall notices by FedEx on December 9, 2013. Foreign customers were sent recall notices by e-mail between December 6 and December 13, 2013. The recall notice instructed customers to return the recalled product.
Root cause
Use error
Status
Terminated
Product code
HQB
Quantity affected
12 units
Distribution
Worldwide Distribution-USA (nationwide) and the countries of Argentina, Austria, Brazil, Canada, China, Egypt, France, Germany, Greece, Hong Kong, Italy, Japan, Mexico, Morocco, the Netherlands, Pakis
Date initiated
2013-12-09
Date posted
2014-01-30
Date terminated
2015-03-25
Location
O Fallon, MO

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