Janssen Pharmaceutica, N.V.

FDA Regulatory Profile

Janssen Pharmaceutica, N.V. has 0 FDA recalls, 18 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Nov 21, 2025 · NAI

Newer recall under related name Ethicon: Sep 8, 2026, Z-0153-2027.

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections18Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Related names

NameRecalls510(k)InspectionsComplianceMost recent recall
Ethicon
Same company group
77208150Sep 8, 2026 (Z-0153-2027)
Johnson And Johnson Surgical Vision
Same company group
18490Jul 31, 2026 (Z-3064-2026)
Synthes (Usa) Products
Same company group
1644570Feb 25, 2026 (Z-1703-2026)
Cerenovus
Same company group
110110Oct 2, 2025 (Z-0434-2026)
Ethicon Endo-Surgery
Same company group
5418480Sep 11, 2025 (Z-0147-2026)
Johnson And Johnson Vision Care
Same company group
101230Jun 12, 2025 (Z-2163-2025)
Ethicon Endo Surgery
Same company group
4220Mar 7, 2025 (Z-1516-2025)
Biosense Webster
Same company group
337670Jan 5, 2025 (Z-1205-2025)
Ethicon Sarl, A Johnson And Johnson
Same company group
2020Jun 11, 2024 (Z-2407-2024)
Depuy Orthopaedics
Same company group
155210112Mar 12, 2024 (Z-1456-2024)
Depuy Spine
Same company group
367190May 20, 2022 (Z-1324-2022)
Janssen Pharmaceuticals
Same company group
40322Oct 23, 2018 (D-0218-2019)

Recent FDA Inspections

DateSiteProductClassificationFEI
Nov 21, 2025Beerse, BelgiumDevicesNo Action Indicated (NAI)3002807336
Sep 5, 2025Beerse, BelgiumDrugsVoluntary Action Indicated (VAI)3002807336
May 12, 2025Beerse, BelgiumDrugsVoluntary Action Indicated (VAI)3002807336
Mar 26, 2024Geel, BelgiumDrugsVoluntary Action Indicated (VAI)3002807337
Oct 27, 2022Geel, BelgiumDrugsVoluntary Action Indicated (VAI)3002807337
Jul 2, 2021Beerse, BelgiumDrugsVoluntary Action Indicated (VAI)3002807336
Jun 12, 2018Beerse, BelgiumDrugsVoluntary Action Indicated (VAI)3002807336
Dec 15, 2017Geel, BelgiumVeterinaryNo Action Indicated (NAI)3002807337
Mar 1, 2016Beerse, BelgiumDrugsVoluntary Action Indicated (VAI)3002807336
Jun 4, 2015Geel, BelgiumDrugsNo Action Indicated (NAI)3002807337
May 14, 2014Beerse, BelgiumDrugsVoluntary Action Indicated (VAI)3002807336
Sep 12, 2013Geel, BelgiumDrugsNo Action Indicated (NAI)3002807337
May 2, 2013Beerse, BelgiumDevicesNo Action Indicated (NAI)3002807336
Oct 18, 2012Geel, BelgiumDrugsVoluntary Action Indicated (VAI)3002807337
Sep 27, 2012Beerse, BelgiumDrugsNo Action Indicated (NAI)3002807336
May 6, 2011Geel, BelgiumDrugsNo Action Indicated (NAI)3002807337
Dec 10, 2010Geel, BelgiumDrugsNo Action Indicated (NAI)3002807337
Dec 18, 2009Beerse, BelgiumDrugsVoluntary Action Indicated (VAI)3002807336

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.

FDA-Inspected Facilities

FacilityLocationInspectionsLatest
FEI 3002807336Beerse, Belgium10Nov 21, 2025
FEI 3002807337Geel, Belgium8Mar 26, 2024

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