Mercy Hospital St Louis Blood Bank FDA Record

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

  • Latest inspection NAI · Aug 20, 2024
  • No warning letters matched by name
Inspections 8 0 OAI
Recalls 0 0 Class I
Warning letters 0 None on file
510(k) clearances 0 None on file

Mercy Hospital St Louis Blood Bank has 0 FDA recalls, 8 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Mercy Hospital St Louis Blood Bank" is on file.

What these totals cover: FDA records filed under the name "Mercy Hospital St Louis Blood Bank".

Latest inspection
Aug 20, 2024 · NAI

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 11, 2026 (checked Nov 15, 2026, unchanged)File dated Nov 10, 2026Current
510(k) clearances0Nov 15, 2026File dated Nov 9, 2026Current
Inspections8Nov 15, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

Mercy Hospital St Louis Blood Bank's FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Mercy Hospital St Louis Blood Bank: FDA inspections per year

YearInspectionsOAIWarning lettersRecall recordsClass I
202600000
202500000
202410000
202300000
202200000
202100000
202000000
201910000
201800000
201700000

Inspections are counted by the date they ended, warning letters by the date FDA issued them and recall records by the recall start date. FDA lists one recall record per recalled product, so one recall event can add several.

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Recent FDA inspections

8 inspections from Jun 18, 2009 to Aug 20, 2024.

DateSiteProductClassificationFEI
Aug 20, 2024Creve Coeur, MOBiologicsNo Action Indicated (NAI)1974608
Jan 18, 2019Creve Coeur, MOBiologicsNo Action Indicated (NAI)1974608
Oct 21, 2016Creve Coeur, MOBiologicsNo Action Indicated (NAI)1974608
Nov 7, 2014Creve Coeur, MOBiologicsNo Action Indicated (NAI)1974608
Nov 1, 2013Creve Coeur, MOBiologicsNo Action Indicated (NAI)1974608
Mar 21, 2012Creve Coeur, MOBiologicsNo Action Indicated (NAI)1974608
Feb 16, 2011Creve Coeur, MOBiologicsVoluntary Action Indicated (VAI)1974608
Jun 18, 2009Creve Coeur, MOBiologicsNo Action Indicated (NAI)1974608
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.

FDA-inspected facilities

1 inspected site, newest inspection first.

FacilityLocationInspectionsLatest
FEI 1974608Creve Coeur, MO8Aug 20, 2024

Mercy Hospital St Louis Blood Bank and the FDA: common questions

Has Mercy Hospital St Louis Blood Bank received an FDA warning letter?

No FDA warning letter addressed to the name "Mercy Hospital St Louis Blood Bank" is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has Mercy Hospital St Louis Blood Bank received an FDA Form 483?

FDA has not published a Form 483 for "Mercy Hospital St Louis Blood Bank" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Mercy Hospital St Louis Blood Bank?

The most recent FDA inspection on file ended Aug 20, 2024 at Creve Coeur, MO and was classified NAI. FDA has 8 inspections of Mercy Hospital St Louis Blood Bank on file.

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