Teleflex Medical De Tecate, S. De R.L De C.V. (A Teleflex Medical Company)

FDA Regulatory Profile

Teleflex Medical De Tecate, S. De R.L De C.V. (A Teleflex Medical Company) has 0 FDA recalls, 2 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Dec 9, 2022 · NAI

Newer recall under related name Teleflex: May 7, 2026, Z-2639-2026.

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances0Oct 4, 2026Not statedCurrent
Inspections2Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Related names

NameRecalls510(k)InspectionsComplianceMost recent recall
Teleflex
Same company group
1511090May 7, 2026 (Z-2639-2026)
Teleflex Medical
Same company group
2364170Apr 11, 2022 (Z-1127-2022)

Recent FDA Inspections

DateSiteProductClassificationFEI
Dec 9, 2022Tecate, MexicoDevicesNo Action Indicated (NAI)3003898360
Jan 12, 2012Tecate, MexicoDevicesVoluntary Action Indicated (VAI)3003898360

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.