Class II — Applied Medical Resources Corp
| Recalling firm | APPLIED MEDICAL RESOURCES |
|---|---|
| Registered facility | View this company's 3 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | There is the potential for extended length of the blade obturator after assembly into the cannula and seal housing. |
| Product | Kii Low Profile, Bladed Dual Pack , Qty. 1 5x55mm REF: CTB23 |
| Quantity | 450 units |
| Distribution | US: MI, CA, ME, OUS: France Great Britain, Germany |
| Initiated | 2025-12-11 |
| Classified | 2026-01-02 |
| Recall number | Z-1010-2026 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Applied Medical Resources Corp (Z-1010-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/98191/
Alerts for APPLIED MEDICAL RESOURCES
Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.
Want a one-page facility brief?
A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.