Reported May 23, 2018 · Terminated
(1) BOX KITDE0143 BYPASS BOX (Item Number: KITDE0143, KITDE0143 BYPASS BOX) (2) BOX KITDE0154 BYPASS KH NORDWEST (Item…
Covidien Medtronic
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: COVIDIEN MEDTRONIC · 60 NIDDLETOWN AVE 2ND F · NORTH HAVEN, CT · 06473
Is this the product you have?
- (1)
- BOX KITDE0143 BYPASS BOX (Item Number
KITDE0143KITDE0143 BYPASS BOX) (2) BOX KITDE0154
- BYPASS KH NORDWEST (Item Number
KITDE0154KITDE0154
- BYPASS KH NORDWEST Product UsageThe Endo GIA universal and Endo GIA universal XL staplers place two, triple-staggered rows of titanium staples and simultaneously divides the tissue between the two, triple-staggered rows. The size of the staples is determined by the selection of the 2.0 mm, 2.5 mm, 3.5 mm or 4.8 mm single use loading unit. The Endo GIA universal staplers will accommodate any of the single use loading unit sizes that are available in the 30 mm, 45 mm and 60 mm lines
- Lot codes and dates
- Lot Numbers
(1) 02144636340215280952 (2) 02140138870214144177021426019402144707670214956044 0214620382021474495702150791030215151206
- Lot Numbers
- Amount recalled
- 171,271 units in total
This recall covers 40 products
The agency filed one notice per product. You are reading one of them; the other 39 are below.
27 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Device may be missing a sled component. The sled component is responsible for staple deployment. This may result in failure to form a staple line when tissue is divided, leading to bleeding or leakage of luminal contents.
This product could cause temporary or reversible health problems — stop using it.
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