Class II — T.A.G. MEDICAL PRODUCTS CORPORATION, LTD.
| Recalling firm | F & L MEDICAL PRODUCTS LLC |
|---|---|
| Registered facility | F & L MEDICAL PRODUCTS LLC (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | There is potential for the blister tray to be cracked causing the sterile barrier to be compromised and potential for particulate within the sterile barrier. |
| Product | FlipCutter III Drill |
| Quantity | 6625 units |
| Distribution | Product distributed throughout the United States, Austria, Australia, Bermuda, Switzerland, China, Germany, Denmark, France, Great Britain, Italy, Netherlands, Poland, Sweden and Taiwan. |
| Initiated | 2020-01-20 |
| Classified | 2020-03-20 |
| Terminated | 2025-04-21 |
| Recall number | Z-1542-2020 |
| 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 — T.A.G. MEDICAL PRODUCTS CORPORATION, LTD. (Z-1542-2020).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/85019/
Alerts for F & L MEDICAL PRODUCTS LLC
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.