Evenflo Company, Inc. FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

Evenflo Company, Inc. has 0 FDA recalls, 3 inspections, 11 510(k) clearances and 1 compliance action on record. FDA has issued 1 warning letter to Evenflo Company, Inc., the most recent on Aug 25, 2009.

What these totals cover: FDA records filed under the name "Evenflo Company, Inc." and its spelling variants "Evenflo Company", "Evenflo Co".

Latest inspection
Jan 17, 2013 · NAI
Latest 510(k)
Dec 22, 2010

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances11Nov 8, 2026File dated Nov 2, 2026Current
Inspections3Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

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Evenflo Company, Inc. FDA Warning Letters

1 warning letter on Aug 25, 2009.

IssuedSubjectIssuing officeClose-out letter
Aug 25, 2009 · Record page

A warning letter is FDA's formal notice that a company has violated FDA requirements. Each date links to the letter on fda.gov where FDA has it online. Search the text of every letter with the FDA warning letter search.

Recent FDA inspections

3 inspections from Feb 2, 2009 to Jan 17, 2013.

DateSiteProductClassificationFEI
Jan 17, 2013Miamisburg, OHDevicesNo Action Indicated (NAI)3001329238
Mar 4, 2010Miamisburg, OHDevicesNo Action Indicated (NAI)3001329238
Feb 2, 2009Miamisburg, OHDevicesOfficial Action Indicated (OAI)3001329238
NAI
No objectionable conditions or practices were found during the inspection.
VAI
Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
OAI
Regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

Compliance Actions

FDA's compliance actions data lists 1 compliance action under Evenflo Company, Inc.: warning letters, injunctions and seizures. None came from FDA's Center for Tobacco Products.

Most recent: Warning Letter, Aug 25, 2009.

The warning letters in this data are listed above, together with the letters FDA posts online; a letter found in both is shown once. Other actions are not listed on this page. Search them with the FDA warning letter search or browse all compliance actions.

FDA-inspected facilities

1 inspected site, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3001329238Miamisburg, OH3Jan 17, 2013

Recent 510(k) clearances

11 510(k) clearances from Jul 22, 1996 to Dec 22, 2010.

K-NumberDeviceDate
K102600SIMPLYGO BREAST PUMPDec 22, 2010
K100435AMEDA PLATINUM BREAST PUMPMay 28, 2010
K092770SIMPLYGO HANDS FREE BREAST PUMPOct 9, 2009
K082307EVENFLO COMFORT SELECT PERFORMANCE BREAST PUMP KITSep 11, 2008
K053493BERRY FRUITY TEETHERFeb 22, 2006
K052909EVENFLO ELAN BREAST PUMPNov 1, 2005
K022933EVENFLO COMFORT SELECT AUTO-CYCLE BREAST PUMP KITDec 2, 2002
K013226EVENFLO COMFORT EASE MANUAL BREAST PUMP KITDec 20, 2001
K983776EVENFLO COMFORT CONTROL BREAST PUMP, EVENFLO COMFORT CONTROL DUAL BREAST PUMPApr 26, 1999
K960727EVENFLO NATURAL MOTHER ELECTRIC BREAST PUMP KITFeb 14, 1997
K960726EVENFLO SOFT-TOUCH ULTRA BATTERY OPERATED BREAST PUMPJul 22, 1996

Evenflo Company, Inc. and the FDA: common questions

Has Evenflo Company, Inc. received an FDA warning letter?

Yes. FDA has issued 1 warning letter to Evenflo Company, Inc.. The most recent is dated Aug 25, 2009.

Has Evenflo Company, Inc. received an FDA Form 483?

FDA has not published a Form 483 for "Evenflo Company, Inc." in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Evenflo Company, Inc.?

The most recent FDA inspection on file ended Jan 17, 2013 at Miamisburg, OH and was classified NAI. FDA has 3 inspections of Evenflo Company, Inc. on file, 1 of them classified OAI (official action indicated).

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Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.