Slider Needle 45° Left CRecalls & reported problems

T.A.G Medical Products Agricultural Cooperative Association · Class 1

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 10810190015527), received between Nov 3, 2020 and Nov 3, 2020 — 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.

Most reported problems

Device problems

Break1

Patient problems

Foreign Body In Patient1

Recent adverse event reports

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

MalfunctionNov 3, 2020Break; Break
SLIDER NEEDLE SNAPPED AT DISTAL TIP IN PATIENT.
Patient problems: Foreign Body In Patient
MAUDE report 10777402 ↗

Device details

UDI-DI	`10810190015527`
Brand	Slider Needle 45° Left
Model	C
Catalog no.	500752st
Company	T.A.G Medical Products Agricultural Cooperative Association
Product code	HWQ · Passer
Class	Class 1
FDA submission	None listed
Implant	No
Rx / OTC	—
Single use	Yes
Sterile	Yes
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Dec 4, 2020

Device type (GMDN): Suturing unit, single-use

A non-powered, hand-held device intended to pass sutures or a needle/suture assembly through tissues/prosthetic materials to facilitate suturing during an endoscopic and/or open surgical procedure; it may also knot, cut and/or tighten the sutures/ligature loop during or after placement. It typically consists of a shaft with hooks, catches, clasps, or forceps-like jaws at the distal end, and a proximal handle with controls. It typically has a pointed/cutting component to create a suture tunnel, and is loaded with the sutures or the suture is inserted through the shaft. This is a single-use device.

Other Passer devices

NA 7209485
Smith & Nephew, Inc. · PASSER
202 reports
FIRSTPASS 22-4038
Smith & Nephew, Inc. · PASSER
189 reports
FIRSTPASS 22-4035
Smith & Nephew, Inc. · PASSER
67 reports
NanoPass CAT02298
Stryker Corporation · PASSER
15 reports
NA 7210752
Smith & Nephew, Inc. · PASSER
13 reports
ENDOBUTTON 014396
Smith & Nephew, Inc. · PASSER
10 reports
SlingShot CAT02590
Stryker Corporation · PASSER
8 reports
NA 014395
Smith & Nephew, Inc. · PASSER
5 reports

All Passer 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