Grip-Lok 3200SRecalls & reported problems

Tidi Products, LLC · Small Universal Securement Device, For lines and tubes sized 4.5-13.5 Fr · Class 2

All models of Grip-Lok (11)

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

Adverse event reports: 2
Deaths reported: 0
Injuries reported: 0
Recalls naming it: 0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00618125134656), received between Jun 15, 2023 and Jun 15, 2023 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Loss of or Failure to Bond” (2 reports).

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

Loss of or Failure to Bond2

Patient problems

No Clinical Signs, Symptoms or Conditions2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

MalfunctionJun 15, 2023Loss of or Failure to Bond; Loss of or Failure to Bond
5/19/23-LK MCARTHUR COMPLAINT #: (B)(4) GRIP-LOK NOT SECURELY TUBES. HAVE HAD 2 INCIDENTS OF ABDOMINAL TUBES FALLING OUT AND 1 CHEST TUBE FALLING OUT. THE TUBES WERE NOT IN FOR LONGER THAN 2 DAYS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17140075 ↗
MalfunctionJun 15, 2023Loss of or Failure to Bond; Loss of or Failure to Bond
5/19/23 MCARTHUR COMPLAINT #: MCA0639 GRIP-LOK NOT SECURING TUBES. HAVE HAD 2 INCIDENTS OF ABDOMINAL TUBES FALLING OUT AND 1 CHEST TUBE FALLING OUT. THE TUBES WERE NOT IN FOR LONGER THAN 2 DAYS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17140012 ↗

Device details

UDI-DI	`00618125134656`
Brand	Grip-Lok
Model	3200S
Company	Tidi Products, LLC
Product code	PLI · Gastrointestional Tube Holder
Class	Class 2
FDA submission	None listed
Implant	No
Rx / OTC	OTC
Single use	Yes
Sterile	Yes
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Apr 22, 2026

Device type (GMDN): Nasogastric tube holder, noninvasive

A small, noninvasive device intended to be used to secure a nasogastric tube to prevent displacement or removal of the tube from the patient. It is typically designed as an adhesive plaster with wings that are attached to the face (e.g., across the bridge of the nose, on the cheeks). It may have a lock-ring or non-adhesive tabs that is/are attached to the nasogastric tube (placed through a nostril and via the oesophagus) to hold it safely and comfortably in place. The lock-ring or tabs can be removed without scissors for easy removal of the tube. This is a single-use device.

Other Gastrointestional Tube Holder devices

Grip-Lok 3400L
Tidi Products, LLC · Gastrointestional Tube Holder
1 report

All Gastrointestional Tube Holder 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.

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