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Ricarimpex Sas FDA Record

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

Ricarimpex Sas has 0 FDA recalls, 0 inspections, 1 510(k) clearance and 0 compliance actions on record. No FDA warning letter addressed to "Ricarimpex Sas" is on file.

What these totals cover: FDA records filed under the name "Ricarimpex Sas" and its spelling variant "Ricarimpex". Records filed under related names are not included; see Related names.

Latest 510(k): Jun 21, 2004

Summary

Record counts and when each FDA source was last refreshed
Records	Count	Last refreshed	Source as of	Status
Recalls	0	Nov 8, 2026	File dated Nov 3, 2026	Current
510(k) clearances	1	Nov 8, 2026	File dated Nov 2, 2026	Current
Inspections	0	Nov 14, 2026	Newest record Nov 5, 2026	Current
Compliance actions	0	Nov 2, 2026	Newest record Oct 29, 2026	Current

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Related names

Each name below has its own page. Its counts cover only the records FDA filed under that name and are not part of the totals for Ricarimpex Sas above.

Name	Relation	Recalls	510(k)	Inspections	Compliance actions	Most recent recall
Ricarimpex Sas	Same company group	0	0	2	0	—

Recent 510(k) clearances

1 510(k) clearance on Jun 21, 2004.

K-Number	Device	Date
K040187	MEDICINAL LEECHES	Jun 21, 2004

Ricarimpex Sas and the FDA: common questions

Has Ricarimpex Sas received an FDA warning letter?

No FDA warning letter addressed to the name "Ricarimpex Sas" 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 Ricarimpex Sas received an FDA Form 483?

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

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