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MEDLINE INDUSTRIES, INC.
MEDLINE INDUSTRIES, INC. · Model MSC6102 · UDI-DI 10080196669790
1
510(k) clearances
4
Adverse events
9
Recalls
39
Facilities
Description
HYDROGEL,SKINTEGRITY,1 OZ,BELLOWS BTL
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
| 2013-07-26 | ASO, LLC | This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility. |
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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.