FDA Device Intelligence
HomeMUNCHKIN, INC. › Munchkin

Munchkin

MUNCHKIN, INC. · Model MKFE0923 Rev 1 · UDI-DI 00735282381850

HGY
10
510(k) clearances
82
Adverse events
2
Recalls
92
Facilities

Description

Munchkin Silicone Breast Pump

Recalls

DateFirmReason
2015-02-12Ameda, Inc.Devices were not sterilized
2015-02-12Ameda, Inc.Devices were not sterilized

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.