Home › BOUND TREE MEDICAL, LLC › Curaplex
Curaplex
BOUND TREE MEDICAL, LLC · Model XT605-BK-EN · UDI-DI 00810071636110
10
510(k) clearances
89
Adverse events (2 deaths)
8
Recalls
334
Facilities
Description
CURAPLEX SAM XT- BLACK EXTREMITY TOURNIQUET FOR AMAZON 1/EA 25EA/CS
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2020-12-28 | Mar-Med Co | A failure can occur if the user attempts to remove the device by partially snipping the edge and pulling on it. The device may tear into two pieces with a portion remaining in plac |
| 2018-05-02 | The Seaberg Company Inc | Based on internal testing, results indicated a possible failure of the stitches securing the buckle to the nylon belt could occur, posing a potential risk when used on a human pati |
| 2018-05-02 | The Seaberg Company Inc | Based on internal testing, results indicated a possible failure of the stitches securing the buckle to the nylon belt could occur, posing a potential risk when used on a human pati |
| 2018-05-02 | The Seaberg Company Inc | Based on internal testing, results indicated a possible failure of the stitches securing the buckle to the nylon belt could occur, posing a potential risk when used on a human pati |
| 2015-08-31 | Pyng Medical Corporation | Once tested, it is required that the tourniquet be returned to its Ready position then placed in its packaging. Each tourniquet was tested for functionality, but in some cases, the |
| 2014-08-05 | ICU Medical, Inc. | ICU Medical is recalling the BD PosiFlush Sterile Field Saline Flush Syringe because some unit packages may exhibit open seals which impacts package sterility and potentially produ |
| 2014-08-05 | ICU Medical, Inc. | ICU Medical is recalling the BD PosiFlush Sterile Field Saline Flush Syringe because some unit packages may exhibit open seals which impacts package sterility and potentially produ |
| 2014-08-05 | ICU Medical, Inc. | ICU Medical is recalling the BD PosiFlush Sterile Field Saline Flush Syringe because some unit packages may exhibit open seals which impacts package sterility and potentially produ |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.