Welch Allyn, Inc. 901110 (REF 4802D-AX-XB)Recalls & reported problems

Welch Allyn, Inc. · 4802D Pediatric Scale / Infant Scale with standard cradle (X), 1 gram accuracy (diaper option) (A) and standard weight (lb/kg) (X) · Class 1

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports: 3
Deaths reported: 0
Injuries reported: 0
Recalls naming it: 0

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00732094227390), received between Jan 6, 2025 and Jul 21, 2026 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Material Split, Cut or Torn” (3 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 18, 2026.

Reports received per month

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

Most reported problems

Device problems

Material Split, Cut or Torn3

Patient problems

No Clinical Signs, Symptoms or Conditions3

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

MalfunctionJul 21, 2026Material Split, Cut or Torn
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25894244 ↗
MalfunctionSep 10, 2025Material Split, Cut or Torn; Material Split, Cut or Torn
CUSTOMER REPORTED THAT THE POWER CORD TO THE SCALE WAS WORN WITH THE COPPER EXPOSED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23015301 ↗
MalfunctionJan 6, 2025Material Split, Cut or Torn; Material Split, Cut or Torn
CUSTOMER REPORTED THE CORD WAS SEPARATED AT THE POWER SUPPLY AND WIRES WERE SHOWING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21080682 ↗

Device details

UDI-DI	`00732094227390`
Brand	Welch Allyn, Inc.
Model	901110
Catalog no.	4802D-AX-XB
Company	Welch Allyn, Inc.
Product code	FRW · SCALE, PATIENT
Class	Class 1
FDA submission	None listed
Implant	No
Rx / OTC	Prescription
Single use	No
Sterile	Yes
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Feb 7, 2020

Device type (GMDN): Infant scale, electronic

An electrically-powered device designed to measure the weight of an infant, particularly a newborn, or to monitor weight changes, e.g., during critical care procedures. It typically consist of a weight tray, a flexure plate or bending beam, an electronic transducer, and an analogue or digital display; it may include markings to also measure infant length. The device is also known as paediatric or baby scale.

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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.

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