FDA applicant

Johnson & Johnson Patient Care, Inc.

New Brunswick, NJ4 decisions1988–19890 recalls

FDA records 4 decisions for Johnson & Johnson Patient Care, Inc. (New Brunswick, NJ) from 1988 to 1989: 4 510(k) clearances. Most are in product codes FRO (Dressing, Wound, Drug) and KYZ (Syringe, Irrigating (Non Dental)). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general hospital panel, where it files most

How often FDA has decided Johnson & Johnson Patient Care, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Johnson & Johnson Patient Care, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Johnson & Johnson Patient Care, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Johnson”

FDA records each applicant name separately; these may or may not be the same firm.

Johnson & Johnson Professionals, Inc. 206 Johnson & Johnson Medical, Inc. 56 Johnson & Johnson Clinical Diagnostics, Inc. 33 Johnson & Johnson Orthopaedics, Inc. 22 Johnson & Johnson Vision Care, Inc. 13 Johnson & Johnson 12 Johnson & Johnson Surgical Vision, Inc. 11 Johnson & Johnson International 10 Johnson & Johnson Consumer Products, Inc. 8 Johnson & Johnson Medical, Div. of Ethicon, Inc. 5 Johnson & Johnson Consumer Companies, Inc. 2 Johnson and Johnson 2

Johnson & Johnson Patient Care, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Johnson”