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Device, Percutaneous, Biopsy
FDA product code MJG · Class 1 · General, Plastic Surgery
727
Registered devices
44
Adverse events
4
Recalls
7
510(k) clearances
Devices with this code
CARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCPalium Needle — M.D.L. S.R.L.CARDINAL HEALTH — Cardinal Health 200, LLCCook — COOK INCORPORATEDCARDINAL HEALTH — Cardinal Health 200, LLCCook — COOK INCORPORATEDGreene — COOK INCORPORATEDCARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCCook — COOK INCORPORATEDCARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLCPalium Needle — M.D.L. S.R.L.CARDINAL HEALTH — Cardinal Health 200, LLCCARDINAL HEALTH — Cardinal Health 200, LLC
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-04-08 | MEDLINE INDUSTRIES, LP - Northfield | Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have bee |
| 2024-03-01 | Cook Incorporated | Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility |
| 2021-08-05 | M.D.L. S.r.l. | Sterility assurance may be compromised. |
| 2010-07-02 | Medical Device Technologies, Inc. | Medical Device Technologies, Inc., dba Angiotech, Gaineville, Florida is recalling Tru-Core II Disposable Biopsy Devices due to compromised packaging integrity |
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