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Integra® Jarit®

INTEGRA LIFESCIENCES PRODUCTION CORPORATION · Model 110195 · UDI-DI 10381780167167

GDZ Prescription
10
510(k) clearances
128
Adverse events
13
Recalls
445
Facilities

Description

Integra® Jarit® Knife Handle, # 3KL, Hexagonal Handle For Minature Blades

Recalls

DateFirmReason
2024-12-03Sklar InstrumentsReports of various packaging issues that may result in a breach of the sterile barrier.
2024-02-23MEDLINE INDUSTRIES, LP - NorthfieldProduct may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
2022-09-02Steris CorporationThe scalpel holder may separate from the handle for certain lots. If the tip falls off during use, it could fall into the patient's mouth which may result in a cut to the patient's
2016-03-11Integra York PA, IncOne lot of self-lock chisel blade handles have a wider slot that holds the chisel blade that may result in the inability to firmly secure the blade in the handle.
2014-09-26Teleflex MedicalThe knife handles slot depth is out of specification, so blades may not fit on the handles properly.
2014-06-24Bard Access SystemsPotential for inadvertent scalpel stick injury involving the safety scalpel.
2013-11-12Ansell Sandel Medical Industries LLCSelect lots of SANDEL Weighted Safety Scalpels are packaged with the scalpel blade exposed beyond the safety shield which could compromise the integrity of the package and the ster
2013-11-12Ansell Sandel Medical Industries LLCSelect lots of SANDEL Weighted Safety Scalpels are packaged with the scalpel blade exposed beyond the safety shield which could compromise the integrity of the package and the ster
2013-11-12Ansell Sandel Medical Industries LLCSelect lots of SANDEL Weighted Safety Scalpels are packaged with the scalpel blade exposed beyond the safety shield which could compromise the integrity of the package and the ster
2013-11-12Ansell Sandel Medical Industries LLCSelect lots of SANDEL Weighted Safety Scalpels are packaged with the scalpel blade exposed beyond the safety shield which could compromise the integrity of the package and the ster

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.