N/A HAR736Recalls & reported problems

Stryker Sustainability Solutions, Inc. · Class U

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports: 1
Deaths reported: 0
Injuries reported: 0
Recalls naming it: 0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327663389), received between May 20, 2026 and May 20, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Reports received per month

Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

Break1
Use of Device Problem1

Patient problems

No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

MalfunctionMay 20, 2026Break; Use of Device Problem
IT WAS REPORTED THE DEVICE WAS OPENED DURING A PROCEDURE AND HAVING AN ISSUE TIGHTENING. BEFORE THE DEVICE WAS USED THE PHYSICIAN AND TECH NOTICED A CHIP IN THE DEVICE JAW. THERE WAS NO PATIENT INJURY, MEDICAL INTERVENTION, OR EXTENDED PROCEDURE TIME REPORTED. THESE ARE COMMONLY USED DEVICES THAT ARE READILY AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25236524 ↗

Device details

UDI-DI	`07613327663389`
Brand	N/A
Model	HAR736
Company	Stryker Sustainability Solutions, Inc.
Product code	NLQ · Single-use reprocessed ultrasonic surgical instruments
Class	Class U
FDA submission	K250898
Implant	No
Rx / OTC	Prescription
Single use	Yes
Sterile	Yes
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Sep 4, 2025

Device type (GMDN): Soft-tissue ultrasonic surgical system holder/tip, reprocessed

A hand-held component of an ultrasonic surgical system which includes a holder with controls and a surgical endpiece (tip) intended to be connected to a system transducer (not included) whereby the tip oscillates (vibrates) at high frequency in order to fragment soft-tissue cells for cutting and/or coagulating tissue during surgery. It may be referred to as a handpiece but does not include a transducer; the tip is available in a variety of forms and sizes, and is typically made of metal. This device is utilized in a variety of surgical disciplines. This is a previously used single-use device that has been processed for an additional single-use patient application.

Other Single-use reprocessed ultrasonic surgical instruments devices

N/A
Stryker Sustainability Solutions, Inc. · Scalpel, ultrasonic, reprocessed
1 recall94 reports
N/A
Stryker Sustainability Solutions, Inc. · Scalpel, ultrasonic, reprocessed
1 recall24 reports
MEDLINE HARH36R
Medline Industries, Inc. · Single-use reprocessed ultrasonic surgical instruments
1 recall24 reports
N/A
Stryker Sustainability Solutions, Inc. · Scalpel, ultrasonic, reprocessed
67 reports
Medline HARH45R
Medline Industries, Inc. · Single-use reprocessed ultrasonic surgical instruments
1 recall2 reports
N/A
Stryker Sustainability Solutions, Inc. · Scalpel, ultrasonic, reprocessed
1 death31 reports
N/A HAR1136
Stryker Sustainability Solutions, Inc. · Single-use reprocessed ultrasonic surgical instruments
24 reports
Medline HAR36MR
Medline Industries, Inc. · Scalpel, ultrasonic, reprocessed
16 reports

All Single-use reprocessed ultrasonic surgical instruments devices →

Sources and updates

Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.

How reports and recalls are matched · Editorial policy · Report an error on this page