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MEDPOR CONTAIN
Stryker Leibinger GmbH & Co. KG · Model 81066 · UDI-DI 07613252084471
NPK
Prescription
1
510(k) clearances
83
Adverse events
1
Recalls
24
Facilities
Description
MEDPOR¿ CONTAIN? Implant Sheet
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-03-01 | Inion Ltd. | Aluminum pouch seal was noticed to be defective (slightly open). |
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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.
