FDANovember 13, 2020device

Resect. Intest. Laparo-LF, Model DYNJ42667A - Product Usage: This is a type of convenience kit used in various surgeries including cardiac, abdominal, and neck surgeries.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The cylindrical sponge component is not x-ray detectable.

What to do

FDA enforcement status: Terminated

Brands named

medline

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Resect. Intest. Laparo-LF, Model DYNJ42667A - Product Usage: This is a type of convenience kit used in various surgeries including cardiac, abdominal, and neck surgeries. — Recall Details · AllClear