Home › APPLIED MEDICAL RESOURCES CORPORATION › DR. GARY LAP CHOLE
DR. GARY LAP CHOLE
APPLIED MEDICAL RESOURCES CORPORATION · Model K2738 · UDI-DI 30607915134359
0
510(k) clearances
508
Adverse events
7
Recalls
78
Facilities
Description
Kit Contains: CA090, DIRECT DRIVE® LCA 3/BX CD001, 10mm RETRIEVAL SYSTEM, 10/BX C0R47, 12x100 Kii® BALLOON BLUNT TIP 6/BX CFS02, 5x100 Kii® SLEEVE ADVFIX 12/BX CFB03, 5x100 Kii® SH BLD ADVFIX, 6/BX CB010, 5MMx34CM SCISSOR REPOS CRTR 10/BX C4120, 38CM GRASPER REPOS CART, 10/BX CTB73, 12x100 Kii® SH BLD ZTHR 6/BX
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2020-03-17 | Applied Medical Resources Corp | There may be a slightly protruding rivet on the distal end of the laparoscopic grasper which has the potential for tissue to catch on it during use and lead to tissue damage. |
| 2020-03-17 | Applied Medical Resources Corp | There may be a slightly protruding rivet on the distal end of the laparoscopic grasper which has the potential for tissue to catch on it during use and lead to tissue damage. |
| 2020-03-17 | Applied Medical Resources Corp | There may be a slightly protruding rivet on the distal end of the laparoscopic grasper which has the potential for tissue to catch on it during use and lead to tissue damage. |
| 2020-03-17 | Applied Medical Resources Corp | There may be a slightly protruding rivet on the distal end of the laparoscopic grasper which has the potential for tissue to catch on it during use and lead to tissue damage. |
| 2017-04-25 | Cook Inc. | reprocessing instructions do not provide sufficient detailed information for the cleaning, disinfection, and sterilization of these products |
| 2015-12-01 | JosNoe Medical, Inc. | Damage to package seals potentially compromising sterility. |
| 2013-05-01 | Applied Medical Resources Corp | Applied Medical is conducting a voluntary recall on specific lot numbers of its Epix and Direct Drive Laparoscopic Graspers. When the ratchet trigger is activated, if a great enoug |
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.