Philips Avent Manual Breast Pump SCF430/03Recalls & reported problems

Philips Consumer Lifestyle B.V. · Trade Item: 884043003540 The Philips Avent manual breast pump is intended to express and to collect milk from the breast of a lactating woman. The device is intended for a single user. INCLUDES: 1x PUMP BODY, 1x NATURAL BOTTLE, 1x SEALING DISC, 1x SCREW RING · Class 1

Data updated Oct 18, 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 00075020109453), received between Aug 29, 2025 and Aug 29, 2025 — classified as 1 malfunction.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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 18, 2026.

Reports received per month

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

Most reported problems

Device problems

Insufficient Device Problem Information1

Patient problems

Breast Discomfort/Pain1

Recent adverse event reports

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

MalfunctionAug 29, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
CUSTOMER CLAIMS THAT THE MANUAL BREAST PUMP CAUSED MASTITIS. THE DEVICE HAS BEEN TESTED AND BEEN FOUND PERFORMING ACCORDING TO SPECIFICATIONS. NO ANOMALIES HAVE BEEN DETECTED ON THE DEVICE.
Patient problems: Breast Discomfort/Pain
MAUDE report 22920702 ↗

Device details

UDI-DI	`00075020109453`
Brand	Philips Avent Manual Breast Pump
Model	SCF430/03
Company	Philips Consumer Lifestyle B.V.
Product code	HGY · Pump, Breast, Non-Powered
Class	Class 1
FDA submission	None listed
Implant	No
Rx / OTC	OTC
Single use	No
Sterile	No
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Jun 4, 2025

Device type (GMDN): Breast pump, manual

A hand-held device used to extract milk from the breast, typically for collecting and feeding to an infant. The device produces a low-grade suction through a funnel-like component that is applied to the breast and is typically operated by the donor; the milk collects in an attached vessel (e.g., a sterilized bottle). This is a reusable device.

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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