FDASeptember 28, 2022device

Endo Stitch V-Loc 180 Absorbable Reload, Models VLOCA004L, VLOCA006L, VLOCA008L, VLOCA204L, VLOCA206L, VLOCA208L, VLOCA304L, VLOCA306L, VLOCA308L. Automated suturing device.

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

The hazard

Medtronic has received 210 reports of needles breaking during endoscopic suturing. The potential harm(s) include a delay in treatment/therapy, the potential for a portion of the needle to remain in the patient, foreign body reaction, allergic reaction, tissue injury and unintended radiation exposure from additional imaging for both intra-op and postoperative scenarios.

What to do

FDA enforcement status: Ongoing

Brands named

covidien lpcovidiencovidien lp

UPCs

208845210680842088452106809120884521068275208845210681142088452106812120884521068282208845210681382088452106815220884521068787

Recall history

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

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Endo Stitch V-Loc 180 Absorbable Reload, Models VLOCA004L, VLOCA006L, VLOCA008L, VLOCA204L, VLOCA206L, VLOCA208L, VLOCA304L, VLOCA306L, VLOCA308L. Automated suturing device. — Recall Details · AllClear