Hollister Incorporated
Hollister Incorporated holds FDA 510(k) medical device clearances, first cleared 2011, most recent 2026, with 5 FDA device recalls on record.
Top product codes for Hollister Incorporated
FDA recalls by Hollister Incorporated
- Z-1179-2025 — AnchorFast SlimFit, Oral Endotracheal Tube Fastener, REF 9787,
- Z-1180-2025 — AnchorFast, Oral Endotracheal Tube Fastener, REF 9799,
- Z-1178-2025 — AnchorFast Guard Select, Oral Endotracheal Tube Fastener, REF 9700,
- Z-1181-2025 — AnchorFast Guard, Oral Endotracheal Tube Fastener, REF 9800,
- Z-1311-2021 — Vertical Drain Tube Attachment Device (VTAD) (Gastrointestinal tube and accessories) - Product Usage: designed to stabilize and secure a variety of catheters, surgical drains, and tubes from sizes 5-40 French.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Hollister Incorporated
- K253295 — Coude Sleeved IC; Coude Plus Sleeved IC
- K251468 — Sleeved IC 3 Family Sleeved IC 3 SWT (name not finalized) Sleeved IC 3 Pocket (name not finalized) Sleeved IC 3 Plus (name not finalized) Sleeved IC 3 Plus Pocket (name not finalized) (N/A)
- K233524 — Sleeved IC 2 Family +4 more
- K220667 — Sleeved IC
- K213575 — Female IC (Not Finalized)
- K211436 — Intermittent Catheter (Not Finalized)
- K193148 — VaPro Plus Pocket, VaPro Plus
- K191633 — Infyna Chic
- K183253 — ValPro 2 Plus, VaPro 2 Plus Pocket
- K180824 — VaPro 2 Intermittent Catheter
- K163179 — Onli Intermittent Catheter
- K152268 — VAPRO PLUS POCKET Intermittent Catheter
- K143594 — VaPro Pocket
- K141642 — VAPRO INTERMITTENT CATHETER
- K110862 — VAPRO PLUS INTERMITTENT CATHETER
Data sourced from openFDA. This site is unofficial and independent of the FDA.